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โ | journal
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stringlengths 0
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โ | abstract_en
stringclasses 100
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โ | url
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stringlengths 23
23
|
|---|---|---|---|---|---|---|---|---|---|---|---|---|
ART000852409
|
oai_dc
|
๊ธ์ฑ ์ท์ฅ์ผ ๋ฐ๋ณ์ผ๋ก ์ง๋จ๋ ์ IVaํ ๋ด๊ด ๋ญ์ข
1๋ก
|
A Case of Type IVa Choledochal Cyst Presented with Acute Pancreatitis
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์กฐํ์ (ํ์๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852410
|
oai_dc
|
Laurence-Moon-Biedl ์ฆํ๊ตฐ 1๋ก
|
A Case of Laurence-Moon-Biedl Syndrome
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ ํ๊ทผ(์์ฒํฅ๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852403
|
oai_dc
|
์์ฒด ๋ถ๋ถ ๊ฐ์ด์์์ De Novo Hepatitis B์ ๋ํ Bํ ๊ฐ์ผ ๋ฉด์ญ๊ธ๋ก๋ถ๋ฆฐ์ ์๋ฐฉ์ ํจ๊ณผ
|
Efficacy of Hepatitis B Immune Globulin for Prevention of De NovoHepatitis B in Living-related Liver Transplantation
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊น์์ข
(์ฑ๊ท ๊ด๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852399
|
oai_dc
|
์์ Helicobacter pylori ๊ฐ์ผ์์ ๊ท ์ ์ ์ ํ, ์ ์ํผ์ธํฌ์ ์ฆ์๊ณผ ์ธํฌ์ฌ
|
The Genotypes of Helicobacter pylori, Gastric Epithelial CellProliferation and Apoptosis in Children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ ์ง์(ํ๋ฆผ๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852400
|
oai_dc
|
์์์์ ์์ฉ๋ ์์คํผ๋ฆฐ์ ์ฅ๊ธฐ๊ฐ ์ฌ์ฉ์ ์ํ ์ยท์ฅ๊ด ์ถํ ์ํ์ฑ์ ๋ํ ์ฐ๊ตฌ
|
Risk of Gastrointestinal Bleeding Associated with Use ofLow-dose Aspirin in Korean Children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋ฐฐ์ ํ(์์ง์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852402
|
oai_dc
|
Hirschsprung๋ณ์์ ํญ๋ฌธ์ง์ฅ ๋ด์๊ฒ์ฌ์ ์ง๋จ์ ์ ์ฉ์ฑ
|
Diagnostic Efficacy of Anorectal Manometry for theDiagnosis of Hirschsprung's Disease
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ฅ์ํฌ(์ธ์ฐ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852411
|
oai_dc
|
Duarte Variant/Classical Galactosemia (D/G) Heterozygote ํ์์์ Galactose-1-Phosphate Uridyltransferase (GALT) Gene์ ๋ํ ์ ์ ์ ๋ถ์ 1๋ก
|
Analysis of the Galactose-1-Phosphate Uridyltransferase (GALT) Gene ina Duarte Variant/classical Galactosemia (D/G) Compound Heterozygote
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ํ๋(์์ธ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART001279466
|
oai_dc
|
์ธํฐํ๋ก ์น๋ฃ์ ๋ฐ์์ด ์์๋ ์์์ ๋ง์ฑ Bํ ๊ฐ์ผ์ ๋ํ ๋ผ๋ฏธ๋ถ๋์ ์น๋ฃ ํจ๊ณผ
|
Effect of Lamivudine Treatment on Chronic Hepatitis B Infection in Children Unresponsive to Interferon
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ฐ๊ท๋ฏผ(๋ถ์ฐ๋ํ๊ต); ๊นํ์(๋ถ์ฐ๋ํ๊ต); ๋ฐ์ฌํ(๋ถ์ฐ๋ํ๊ต)"
] |
Purpose: Interferon is a widely used treatment for chronic hepatitis B in children. However, additional treatment options are needed because more than 50% of hepatitis B patients are unresponsive to interferon. Although lamivudine is widely used to treat hepatitis B, there are few studies on the effect of lamivudine in hepatitis B patients unresponsive to interferon. Methods: Eight interferon unresponsive patients (6 males and 2 females) were treated with lamivudine (3 mg/kg/day, maximum 100 mg/day) from 6โผ12 months after interferon treatment was discontinued among 33 children with chronic hepatitis B. They were treated with interferon (interferon ฮฑ-2b, 10 MU/m2 or pegylated interferon 1.5ฮผg/kg) for 6 months from January 2000 to December 2007 at the Pusan National University Hospital. The medical records were analyzed retrospectively. Results: The age at treatment with interferon and lamivudine was 4.9ยฑ3.1 and 6.1ยฑ3.2 years, respectively. The serum ALT level before treatment with interferon was 148.1ยฑ105.8 IU/L and the log HBV-DNA PCR mean value was 6.95ยฑ0.70 copies/mL. The serum ALT level after treatment with interferon was 143.1ยฑ90.4 IU/L and the log HBV-DNA mean PCR value was 6.46ยฑ2.08. HBeAg negativization occurred in 2 patients. For all patients, normalization of the serum ALT levels and HBeAg seroconversion (except 2 patients with HBeAg negativization) occurred at 7.4ยฑ2.1 and 7.9ยฑ2.1 months respectively after lamivudine treatment. The HBV-DNA PCR became negative in 7 patients (87.5%) at 2.4ยฑ2.8 months. Complete response was achieved in 7 patients and no recurrence was observed in 2 patients for 3 years after the completion of treatment. Five patients are still under treatment for a mean treatment duration of 24.4ยฑ9.1 months. In one patient, viral breakthrough occurred and the treatment was stopped. Conclusion: The number of patients was small, however, lamivudine treatment in patients with chronic hepatitis B who were unresponsive to interferon was highly effective.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279511
|
oai_dc
|
์ฒญ์๋
๊ธฐ์ ๊ฐ๊ฒฝํ์ฆ์ผ๋ก ์งํ๋ ๋น์์ฝ์ฑ ์ง๋ฐฉ๊ฐ์งํ 1์
|
Nonalcoholic Fatty Liver Disease Progressing to Cirrhosis in an Obese Boy with Hypopituitarism
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋ฐ์ง์ฉ(์์ธ๋ํ๊ต); ๊ณ ์ฌ์ฑ(์์ธ๋ํ๊ต); ์ด๋(๊ฑด๊ตญ๋ํ๊ต); ์ ์ถฉํธ(์์ธ๋ํ๊ต); ๊ฐ๊ฒฝํ(์์ธ๋ํ๊ต); ๊น์ฐ์ (์์ธ๋ํ๊ต); ์์ ๊ธฐ(์์ธ๋ํ๊ต)"
] |
Non-alcoholic fatty liver disease (NAFLD) is typically associated with obesity and insulin resistance. Non-alcoholic steatohepatitis (NASH) is a more serious form of NAFLD. Although fibrosis is common in pediatric NASH, cirrhosis has been rarely reported. Patients with hypothalamic or pituitary dysfunction are at risk for obesity and insulin resistance with subsequent development of NAFLD. We report a case of NAFLD progressing to cirrhosis in an obese 16 year-old boy with hypopituitarism.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279526
|
oai_dc
|
์์ ๋ณํ์ ๊ตฌํ ๋ฅผ ์ฃผ์๋ก ๋ด์ํ Grayanotoxin Intoxication 1์
|
A Case of Grayanotoxin Intoxication Presenting with Mental Changes and Vomiting
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊น๊ท๋ฆฌ(์์ง๋ํ๊ต); ๊น๋์(์์ง๋ํ๊ต); ์ดํฌ์ฐ(์์ง๋ํ๊ต); ์์๋ฏผ(์์ง๋ํ๊ต); ์์งํ(์์ง๋ํ๊ต)"
] |
Rhododendron species is one of the largest and most diverse genera in the plant kingdom, comprising over 800 species and existing all over the globe. Grayanotoxin intoxication is caused by ingestion of honey and flowers. Grayanotoxin exists in honey, flowers, pollen, and nectar of the Rhododendron species. Grayanotoxin-intoxicated patients may present with nausea, vomiting, dizziness, weakness, hypotension, bradycardia, and syncope for several hours. We report a case of grayanotoxin intoxication associated with mental changes. A 9-year-old male presented with impaired consciousness and delirium 26 hours after eating about 10 rhododendron sclippenbachii flowers. A brain MRI and EEG were normal. Parenteral fluids were administered and these symptoms resolved completely in 17 hours.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279512
|
oai_dc
|
ํ๋์ค๋ฆฐ์ผ๋ก ์์นํ ๋ฒ์ฏ ์ค๋
์ ์ํ ์์ ๊ธ์ฑ ๊ฐ๋ถ์ 1์
|
A Case of Hyperacute Liver Failure from Mushroom Intoxication in a Child Treated with Penicillin
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊ณฝ๋ณ์ฅ(๊ฑด๊ตญ๋ํ๊ต); ๋ฐฐ์ ํ(๊ฑด๊ตญ๋ํ๊ต)"
] |
Hyperacute liver failure from mushroom intoxication in children is rare and has a low survival rate. We report a case of hyperacute liver failure from mushroom intoxication in a 29-month-old boy. The patient ingested a mushroom about three days prior to presentation. He was admitted to the hospital with vomiting, abdominal pain, seizures, and hematemesis. During the hospitalization the patient developed hepatic encephalopathy (stage IV-a), and a coagulopathy. He recovered fully with specific medication, Penicillin GK and N-acetylcysteine.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279516
|
oai_dc
|
์ผ์ฆ์ฑ ๊ฑฐ์ง ์ข
์์ผ๋ก ์ค์ธ๋ ๊ฐ ๋ด ๋ฐ์ํ ์์์ ๊ฒฝ์ธ๋ฐฐ์ฝ์ข
์
|
Primitive Neuroectodermal Tumor of the Liver in a 13-year-old Boy: A Case Report
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ด์๊ตฌ(์ฑ๊ท ๊ด๋ํ๊ต); ๊น์ง์(์ฑ๊ท ๊ด๋ํ๊ต); ์ด์งํ(์ฑ๊ท ๊ด๋ํ๊ต); ์ดํ์ง(์ฑ๊ท ๊ด๋ํ๊ต); ์ด์ข
์น(์ฑ๊ท ๊ด๋ํ๊ต); ์ด์งํ(ํ๋ฆผ๋ํ๊ต); ์ต์ฐํธ(์ฑ๊ท ๊ด๋ํ๊ต)"
] |
Primary primitive neuroectodermal tumor (PNET) of the liver is a rare disease with aggressive behavior and poor prognosis. We report a case of a PNET of the liver in a 13-year-old boy. The patient was admitted to the hospital with fever and abdominal pain. Abdominal CT and MRI revealed a 5.5 cm sized, septated, non-enhancing mass in the hepatic hilum. The patient was initially diagnosed with an inflammatory pseudotumor. Despite 9 days of antibiotic therapy, the patientโs clinical symptoms did not improve. A liver biopsy was performed in the interest of formulating a differential diagnosis. This procedure revealed tumor cells positive for CD99 on immunohistochemistry. The patient was diagnosed with a PNET.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279492
|
oai_dc
|
์ญ์ทจ ๋ฌธ์ ๊ฐ ์๋ ์์ ์ ์๋์ ๋ํ ๋ถ๋ชจ์ค๋ฌธ์กฐ์ฌ
|
Parental Survey for Children with Feeding Problems
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊นํ์ง(์ฐ์ธ๋ํ๊ต); ๋ฐ๋ฏธ์ (์ธ์ ๋ํ๊ต); ์ต์ฐํธ(์ฑ๊ท ๊ด๋ํ๊ต); ์ ๊ฒฝ๋ฏธ(์ฐ์ธ๋ํ๊ต)"
] |
Purpose: Feeding problems are common for typically developing children and have negative effects on physical, behavioral, and cognitive development. The purpose of the current study was to examine factors related to childhood feeding problems for typically developing children via parental reports. Methods: The feeding questionnaire developed by the authors and the Childhood Eating Behavior Inventory (CEBI) were administered to 796 parents of children who recruited from 2 pediatric outpatient clinics (n=379) and community (n=417). Problem eaters (PE) were identified by parental report and frequency analysis was conducted for types of feeding problems and its severity, problem behaviors during mealtime, the feeding methods of the parents, and the need for treatment. Results: The CEBI scores were significantly different between the PE and non-problem eaters (NPE), which suggests that the parental reports were reliable. The younger children had more feeding problems than the older children. The most frequent and severe feeding problems were selective eating and longer mealtimes across all age groups. One-half of the children had more than one problem behaviors during mealtime. Most parents of PE used ineffective methods to deal with children's behaviors during meal time, such as cajoling, which was related to their increased level of stress. Many parents reported their children need professional help for the feeding problems. Conclusion: Feeding problems are prevalent among children, especially younger children. Children with feeding problems showed a number of problem behaviors during mealtime and parental coping methods appeared to be ineffective. The need for treatment was considerable, thus the characteristics of this population must be acknowledged for providing proper treatment and advice.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279520
|
oai_dc
|
์ ์ ์ ๊ฒ์ฌ๋ก ์ง๋จ๋ ์ 2ํ Crigler-Najjar ์ฆํ๊ตฐ 1์
|
A Case of Crigler-Najjar Syndrome Type 2 Diagnosed UsingGenetic Mutation Analysis
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊น์์ด(์ฐ์ธ๋ํ๊ต); ์ด์ํ(์ฐ์ธ๋ํ๊ต); ๊ณ ํ(์ฐ์ธ๋ํ๊ต); ์ด์นํ(์ฑ๊ท ๊ด๋ํ๊ต); ๊ธฐ์ฐฝ์(์ฑ๊ท ๊ด๋ํ๊ต); ๊น์ข
์(์ฑ๊ท ๊ด๋ํ๊ต); ์ ๊ธฐ์ญ(์ฐ์ธ๋ํ๊ต)"
] |
Crigler-Najjar syndrome is a rare inherited disease associated with unconjugated hyperbilirubinemia. It is inherited via an autosomal recessive pattern and is caused by mutation in one of the five exons of the bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) gene. The synthesis of inactive isoforms of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (B-UGT) results in unconjugated hyperbilirubinemia. A 13-year-old boy with jaundice for 4 months was admitted to our hospital. He had unconjugated hyperbilirubinemia with no evidence of infection, hemolysis, or structural abnormalities on abdominal ultrasonography or 99mTc-DISIDA scan. The authors identified a missense mutation of Tyr486Asp in the fifth exon of the UGT1A1 gene and diagnosed the patient with Crigler-Najjar syndrome type II. This is the first reported case of Crigler-Najjar syndrome in a Korean child, and it is also the first reported case of a genetic mutation leading to Crigler-Najjar syndrome in Korea.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279506
|
oai_dc
|
Blue Rubber Bleb Nevus Syndrome 1์
|
A Case of Blue Rubber Bleb Nevus Syndrome
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊ฐ๊ธฐ์(์ ์ฃผ๋ํ๊ต); ์คํ์ฃผ(์ ์ฃผ๋ํ๊ต); ๊ณ ์ฌ์ฑ(์์ธ๋ํ๊ต); ๋ฐ๊ท์(์์ธ๋ํ๊ต); ๊ฐ๊ฒฝํ(์์ธ๋ํ๊ต); ๊น์ฐ์ (์์ธ๋ํ๊ต); ์์ ๊ธฐ(์์ธ๋ํ๊ต)"
] |
We report a 10-year-old girl with the blue rubber bleb nevus syndrome (BRBNS) who had chronic severe anemia caused by chronic occult bleeding in the gastrointestinal (GI) tract. The patient was admitted to the hospital frequently for recurrent pallor and fatigue since the age of 7 years. Gastroduodenoscopy and capsule endoscopy revealed multiple venous malformations with blood oozing in the stomach, small bowel and colon. The patient was treated by aggressive surgical resection of the 23 vascular malformations in the GI tract. The patient is well without anemia 15 months post surgery.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279455
|
oai_dc
|
์ฅ์ค์ฒฉ์ฆ์์ ๋น์์ ์ ์ ๋ณต์ ์คํจ ์ํ์ธ์
|
Risk Factors for the Failure of Non-operative Reduction of Intussusceptions
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊ณ ๊ด๋ฏผ(๊ณ ๋ ค๋ํ๊ต); ์ก์์ฐ(๊ณ ๋ ค๋ํ๊ต); ์ ๋ณด๊ฒฝ(๊ณ ๋ ค๋ํ๊ต); ํ์ฌ์ค(๊ณ ๋ ค๋ํ๊ต); ์ฐ์ฐฌ์ฑ(๊ณ ๋ ค๋ํ๊ต); ์ต๋ณ๋ฏผ(๊ณ ๋ ค๋ํ๊ต); ์ด์ ํ(๊ณ ๋ ค์ฌ์ด๋ฒ๋ํ๊ต)"
] |
Purpose: Intussusceptions are one of the most common causes of intestinal obstruction in infants and young children. Although it is easily treated by non-operative reduction using barium, water or air, this treatment is very stressful for young patients and may cause bowel perforation, peritonitis and shock. In this study, we identified the risk factors associated with the failure of non-operative reduction, to identify a group of children that would benefit from the procedure and those who would not.
Methods: We reviewed the medical records of patients with intussusception who were treated at the Korea University Medical Center Ansan hospital from March 1998 to July 2006. Three hundred fourteen children with intussusception were identified. Among them, non-operative reductions were performed in three hundred. Clinical and radiological variables were compared according to the failure or success of the non-operative reduction.
Results: Non-operative reductions were successful in 243 (81%) and failed in 57 (19%). The group that had failed procedures had a younger age (12.3ยฑ17.2 months vs. 18.0ยฑ15.8 months, p=0.03), longer symptom duration before reduction (33.6ยฑ29.0 hr vs. 21.5ยฑ20.3 hr, p๏ผ0.01), more vomiting and lethargy (p๏ผ0.01), but less abdominal pain and irritability (p๏ผ0.01), compared with the group that had a successful procedure. Logistic regression analysis showed that the factors associated with the failure of non-operative reductions were a younger age, less than 6 months of age (odds ratio: 2.5, 95% confidence interval: 1.2โผ5.2, p=0.01), duration of symptoms, longer than 24 hrs before reduction (odds ratio: 2.1, 95% confidence interval: 1.2โผ4.2, p=0.03), bloody stool (odds ratio: 4.8, 95% confidence interval: 1.9โผ12.2, p๏ผ0.01), lethargy (odds ratio: 3.4, 95% confidence interval: 1.1โผ10.4, p=0.04), and abdominal pain or irritability (odds ratio: 0.2, 95% confidence interval: 0.1โผ0.4, p๏ผ0.01).
Conclusion: For children with intussusception, an age younger than 6 months, and duration of symptoms more than 24 hrs before reduction, as well as the presence of bloody stools, lethargy and abdominal pain or irritability were variables associated with failure of a non-operative reduction. Knowledge of these variables should be considered in making clinical decisions for therapeutic interventions.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279463
|
oai_dc
|
์์ ๋ง์ฑ Bํ ๊ฐ์ผ ํ์์์ ๋ผ๋ฏธ๋ถ๋์ ์น๋ฃ ํจ๊ณผ
|
Efficacy of Lamivudine Therapy for Chronic Hepatitis B in Children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ด์ํ(์ธ์ฐ๋ํ๊ต); ์ฅ์ฃผ์(์ธ์ฐ๋ํ๊ต); ๊น๊ฒฝ๋ชจ(์ธ์ฐ๋ํ๊ต)"
] |
Purpose: Lamivudine is known to be effective for the treatment of chronic hepatitis B in adults. However, data on lamivudine therapy in pediatrics is limited. The aim of this study was to evaluate the efficacy and durability of lamivudine therapy for chronic hepatitis B in Korean children. Methods: A total of 44 children (27 males and 17 females, ages 6 months to 14.8 years, mean age 6.7 years) with chronic hepatitis B who received lamivudine (3 mg/kg/day, max 100 mg) for at least 12 months were enrolled. We evaluated the serum AST, ALT and serological HBV markers (HBsAg and anti-HBs, HBeAg and anti HBe, and HBV DNA) periodically. Predictive three year cumulative seroconversion rates were obtained using the Kaplan-Meier method. Results: Twenty one (48%) of 44 children achieved seroconversion of HBeAg by three years, while 23 (42%) children did not. HBV DNA was cleared in 34 (77%) children and the serum ALT levels were normalized in 41 children (93%). The three year cumulative seroconversion rates were 60% for HBeAg, and the clearance rates were 76% for HBV DNA. Eighteen children who discontinued lamivudine after HBeAg seroconversion maintained the therapeutic response for three years (treatment duration 13โผ58 months mean 24 months). Viral breakthrough developed in 12 children (27%) during the therapy and the YMDD mutation was documented in 11 children (25%). The mean duration for the development of a mutation was 22.7 months. Loss of HBsAg occurred in 6 children (14%). The pretreatment ALT levels were higher in responders; however, the differences were not statistically significant (p๏ผ0.05). Conclusion: The results of this study showed that lamivudine treatment had a favorable effect and durable therapeutic response in children with chronic hepatitis B. Long term follow-up and alternative therapy are warranted for those patients who do not respond to this treatment.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279485
|
oai_dc
|
6โผ7์ธ ๋น๋ง์์์ ํ์ฒญ ์ง์ง๊ณผ ์์ ์ํ์ ๊ดํ ์ฐ๊ตฌ
|
Serum Lipid Profile and Nutritional Status in 6โผ7 Year Old Obese Children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์์ง์ฐ(์กฐ์ ๋ํ๊ต); ๋ฌธ์ง์(์กฐ์ ๋ํ๊ต); ์ด์ฒ ๊ฐ(์กฐ์ ๋ํ๊ต); ๋ฌธ๊ฒฝ๋(์กฐ์ ๋ํ๊ต)"
] |
Purpose: This study was designed to characterize the nutritional status and assess obesity to determine the relationship between obesity and serum lipid profiles in 6โผ7 year old children. Methods: In 2007, we surveyed 483 children (233 boys and 250 girls) aged 6โผ7 years. The total cholesterol, triglyceride levels and HDL-cholesterol were measured in the fasting state. Dietary information was obtained by a questionnaire. Results: The prevalence of obesity was 9.9%. There was no significant difference between genders. The mean caloric intake was 1,781 kcal in boys and 1,640 kcal in girls. The prevalence of excessive calories was 33% in boys and 30% in girls. The prevalence of a total cholesterol โฅ200 mg/dL was 8.4%, TG โฅ130 mg/dL was 5.0%, LDL-cholesterol โฅ130 mg/dL was 3.1%, and HDL-cholesterol <35 mg/dL was 4.4%. The prevalence of hypertension was 2.1%. There was no significant difference between genders. The systolic blood pressure, triglyceride levels and LDL-cholesterol were significantly related to an increased obesity index (p๏ผ0.05). The mean caloric intake and nutritive component were not related to the obesity index. The obesity group was compared to the control group: for triglycerides โฅ130 mg/dL the odds ratio was 4.08; for LDL-cholesterol โฅ130 mg the odds ratio was 2.85; for a TC/HDL-cholesterol โฅ4.0 the odds ratio was 1.16. The BMI and triglyceride levels in the group with hypertension were higher than control group (p๏ผ0.05). There were significant positive correlations between the BMI and blood pressure as well as the LDL-cholesterol and triglycerides (p๏ผ0.05). The BMI was not correlated with the mean caloric intake or nutrition. Conclusion: The prevalence of hypertension and hyperlipidemia in 6โผ7 year old children was significantly related to an increased obesity index. The management of obesity in 6โผ7 year old children should include a reduction in the risk for hyperlipidemia and hypertension.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279461
|
oai_dc
|
๋ง์ฑ ์ํ๊ธฐ ์งํ ํ์์์ ๋ฏธ๋์์ ๊ฒฐํ๊ณผ ๋ชจ๋ฐ ๊ฒ์ฌ์ ์ ์ฉ์ฑ
|
Trace Elements Deficiency and the Diagnostic Usefulness of Hair Mineral Analysis in Children with Chronic Gastrointestinal Disease
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"ํ์ง๋(์์ธ๋ํ๊ต); ์ด์ ํ(๊ฒฝ๊ธฐ๋๋ฆฝ์๋ฃ์); ์ด๋(๊ฑด๊ตญ๋ํ๊ต); ์ ์ง์ฐ(์์ธ๋ํ๊ต); ๊ณ ์ฌ์ฑ(์์ธ๋ํ๊ต); ์์ ๊ธฐ(์์ธ๋ํ๊ต)"
] |
Purpose: Patients with chronic gastrointestinal disease are at risk for trace element deficiency due to impaired absorption and gastrointestinal loss. The aim of this study was to evaluate the trace element status of patients with gastrointestinal disease by blood and hair analysis, and to determine the usefulness of hair mineral analysis for diagnosing trace element deficiency not detected by a blood test. Methods: An analysis of hair minerals was performed and compared with blood mineral analysis in 13 patients with chronic gastrointestinal disease. The concentration of each element in the hair and blood was compared in the subgroups based on parenteral nutritional support or clinical symptoms. Results: Almost all patients had trace element deficiency. The trace elements deficient in the blood or hair analysis included zinc, selenium and copper. The hair zinc concentration was significantly lower in the group receiving parenteral nutritional support. The hair selenium concentration was statistically associated with the clinical symptoms of hair loss, brittle hair and loss of hair pigmentation. Conclusion: The results of this study suggest that patients with chronic gastrointestinal disease should receive adequate zinc and selenium replacement to avoid trace element deficiency especially when treated with long-term parenteral nutrition. Hair mineral analysis is useful as a complementary tool for the detection of a trace element deficiency.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279480
|
oai_dc
|
์์์ฒญ์๋
๋น๋ง์์ ์ํ์ต๊ด๊ณผ ๋์ฌ์ฆํ๊ตฐ์ ์ฐ๊ด์ฑ
|
The Relationship between Lifestyle and Metabolic Syndromein Obese Children and Adolescents
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์กฐ๊ธฐ์(์ดํ์ฌ์๋ํ๊ต); ๋ฐํ์(์ดํ์ฌ์๋ํ๊ต); ์์ ์(์ดํ์ฌ์๋ํ๊ต)"
] |
Purpose: To assess the relationship between lifestyle and metabolic syndrome in obese children and adolescents. Methods: We retrospectively reviewed the medical records and laboratory results of 109 subjects (7โผ15 years of age) who visited our pediatric obesity clinic between January 2004 and December 2007. They completed the parent- and self-report questionnaire developed by the Committee on Nutrition of the Korean Pediatric Society to assess lifestyle. The metabolic syndrome was defined as having 3 or more of the following metabolic risk factors: obesity, hypertension, serum triglycerides โฅ110 mg/dL, HDL-cholesterol โค40 mg/dL, fasting glucose โฅ110 mg/dL, and insulin โฅ20ฮผIU/mL. Results: All subjects had at least 1 risk factor (obesity). Sixty-three percent of subjects had 2 or more risk factors, 32% of subjects had 3 or more risk factors, and 10% had 4 or more metabolic risk factors. Hypertriglyceridemia (36%), hypertension (32%), hyperinsulinemia (24%), and HDL-hypocholesterolemia (20%) were observed. Fasting blood glucose levels were normal in all subjects. Hypertension was significantly associated with an unbalanced diet and hyperinsulinemia was significantly associated with parental obesity (p๏ผ0.05). Those who ate after 8 PM were at a risk of hypertension (odds ratio, 2.5; 95% CI, 1.0โผ6.1). Those who did not have a preference for exercise were at a risk of hyperinsulinemia (odds ratio, 10.4; 95% CI, 2โผ54.1). Those who watched TV for โฅ3 hours/day were at a risk of metabolic syndrome (odds ratio, 4.8; 95% CI, 1.2โผ18.8). Conclusion: Lifestyle, such as eating late, no preference for exercise, and TV watching โฅ3 hours/day, were related to metabolic syndrome in obese children and adolescents.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279488
|
oai_dc
|
๋ชจ์ ์์ ์์ ์ฒ ๊ฒฐํ๊ณผ ์กฐ๊ธฐ ์ ์ฉ๋ ์ฒ ๋ถ๋ณด์ถฉ์๋ฒ์ ํจ๊ณผ์ ๋ํ ์ฐ๊ตฌ
|
Iron Deficiency and Early, Low-dose Iron Supplementation in Breast-fed Infants
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋
ธ์์ (์ถฉ๋ถ๋ํ๊ต); ๋๋ณด๋ฏธ(์ถฉ๋ถ๋ํ๊ต); ๊น๋ฏธ์ (์ถฉ๋ถ๋ํ๊ต)"
] |
Purpose: The purpose of this study was to determine the efficacy of early low-dose iron supplementation in term breast-fed infants. Methods: Eighty-seven healthy term infants were divided into 3 groups: A, formula-fed; B, breast-fed only; S, breast-fed with iron supplementation (5 mg/day from 2 months of age). We measured ferritin, iron, total iron binding capacity (TIBC), transferrin saturation rate (TFSAT), hemoglobin (Hb), hematocrit (Hct), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), and red cell distribution width (RDW) at birth, 6 months of age, and 12 months of age. Results: 1) At 6 months of age, ferritin, iron, TFSAT, and Hb in Group B were the lowest among the 3 groups, whereas TIBC and RDW were the highest. The incidences of iron deficiency (ID) and iron deficiency anemia (IDA) in Group B were 33% and 30%, respectively, significantly higher than those seen in Groups A (5% and 8%, respectively) and S (7% and 5%, respectively). 2) At 12 months of age, ferritin, TFSAT, Hb, MCV, and MCH in Group B were the lowest among the 3 groups, whereas TIBC and RDW were the highest. Iron and Hct did not differ among the 3 groups. The incidences of ID and IDA in Group B were 64% and 50%, respectively, again significantly higher than those seen in Groups A (4% and 3%, respectively) and S (9% and 7%, respectively). Conclusion: The prevalences of ID and IDA were higher in breast-fed infants than in formula-fed infants, even at 6 months of age. Early and low-dose iron supplementation in breast-fed infants improved iron status and lowered the incidence of iron deficiency anemia in early infancy.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279476
|
oai_dc
|
Lamivudine ๋ด์ฑ ์์ ์ฒญ์๋
๋ง์ฑ Bํ ๊ฐ์ผ์์ Adefovir์ ์น๋ฃ ํจ๊ณผ
|
Therapeutic Efficacy of Adefovir Dipivoxil in Korean Children and Adolescents with Chronic Hepatitis B who have Developed Lamivudine Resistance
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"ํฉ์๊ฒฝ(๊ฒฝ๋ถ๋ํ๊ต); ๋ฐ์ ๋ฏผ(๊ฒฝ๋ถ๋ํ๊ต); ๊น์ ๋ฏธ(๊ฒฝ๋ถ๋ํ๊ต); ๊น์ ์ฅ(๊ฒฝ๋ถ๋ํ๊ต); ๊น์๋ฏธ(๊ฒฝ๋ถ๋ํ๊ต); ์ด์งํ(๊ฒฝ๋ถ๋ํ๊ต); ์กฐ๋ฏผํ(๊ฒฝ๋ถ๋ํ๊ต); ํ์์(๊ฒฝ๋ถ๋ํ๊ต); ๊ถ์์ค(๊ฒฝ๋ถ๋ํ๊ต); ์ต๋ณํธ(๊ฒฝ๋ถ๋ํ๊ต)"
] |
Purpose: To estimate the long-term therapeutic efficacy and safety of adefovir dipivoxil in children and adolescents with chronic hepatitis B who have developed lamivudine resistance. Methods: Sixteen patients (12 boys and 4 girls; ages 4.3โผ20.9 years; mean age 14.2 years) with chronic hepatitis B infection resistant to lamivudine therapy received adefovir (0.3 mg/kg/day, maximal dose 10 mg) orally for at least 9 months between March 2004 and April 2008. Each patient was followed up for a mean period of 27 months (range 9โผ49 months) until April 2008 at Kyungpook National University Hospital in Korea. Therapeutic responses to adefovir were evaluated at 12, 24, 36, and 48 months from the initiation of therapy using the Kaplan-Meier method. Response measurements included ALT normalization, HBV DNA negativization, 2 log10 IU/mL decrement of HBeAg titer, HBeAg loss, and HBeAg/Ab seroconversion rate. Results: Three (18.8%) of the 16 patients treated with adefovir showed HBeAg/Ab seroconversion. Kaplan-Meier estimates of cumulative ALT normalization were 12.5% (12 months), 43.8% (24 months), 63.5% (36 months), and 92.7% (48 months), respectively. Cumulative HBV DNA negativization was 6.7%, 30.0%, 45.6%, and 78.2% at 12, 24, 36, and 48 months, respectively. Cumulative 2 log10 copies/mL decrement of HBeAg titer was 12.5%, 43.8%, 56.3%, and 86.9% at 12, 24, 36, and 48 months, respectively. Cumulative HBeAg loss and HBeAg/Ab seroconversion were 6.7% (12 months) and 22.2% (24 months), respectively. Conclusion: The long-term therapeutic efficacy of adefovir dipivoxil was favorable in children and adolescents with chronic hepatitis B who had developed lamivudine resistance. The long-term use of adefovir should be safe in children.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279501
|
oai_dc
|
์ค๋ ๊ด์ฝ๊ทผ ๊ธฐ๋ฅ ์ด์์ผ๋ก ์ธํ ์์์ ์ฌ๋ฐ ๊ธ์ฑ ์ท์ฅ์ผ 1์
|
Recurrent Acute Pancreatitis Associated with Sphincter of Oddi Dysfunction in a Child
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ต๋ณํธ(๊ฒฝ๋ถ๋ํ๊ต); ๋ฐ์ ๋ฏผ(๊ฒฝ๋ถ๋ํ๊ต); ๊นํธ๊ฐ(๋๊ตฌ๊ฐํจ๋ฆญ๋ํ๊ต); ๊น์ ๋ฏธ(๊ฒฝ๋ถ๋ํ๊ต); ํ์์ง(๊ฒฝ๋ถ๋ํ๊ต); ๊น์ ์ฅ(๊ฒฝ๋ถ๋ํ๊ต); ์กฐ๋ฏผํ(๊ฒฝ๋ถ๋ํ๊ต); ์ต๋ณํธ(๊ฒฝ๋ถ๋ํ๊ต)"
] |
Recent studies suggest that sphincter of Oddi dysfunction (SOD) is one of the possible causes of unexplained recurrent acute pancreatitis in children. A 14-year-old boy who had suffered from idiopathic recurrent acute pancreatitis was diagnosed with SOD. Abdominal ultrasonography, computerized tomography, and magnetic resonance cholangiopancreatography revealed no evidence of stone, tumor, or pancreatic ductal anomaly. Endoscopic retrograde cholangiopancreatography (ERCP) and sphincter of Oddi manometry (SOM) revealed elevated basal pressure and tachyoddia consistent with SOD. Hence, an endoscopic pancreatic sphincterotomy was performed. We report a case of recurrent acute pancreatitis associated with SOD in a child. ERCP and SOM may be considered in patients with multiple unexplained attacks of pancreatic pain and negative abdominal imaging.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279458
|
oai_dc
|
์ ์์ ๋ฐ ์์๊ธฐ ์ค์์ธ๋ ํ์กฐ๋ถ๋ฅ์ ์์์ ๊ณ ์ฐฐ
|
Clinical Features of Cricopharyngeal Incoordination in Newborns and Infants
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"ํ์๋ฏธ(๋ถ์ฐ๋ํ๊ต); ๋ฐ์ฌํ(๋ถ์ฐ๋ํ๊ต)"
] |
Purpose: Cricopharyngeal incoordination is a rare cause of swallowing difficulties in newborns and infants; it is characterized by delayed pharyngeal contractions related to cricopharyngeal relaxation. Dysphagia and repeated aspiration are common findings despite normal sucking. We conducted this study to assess the clinical features of cricopharyngeal incoordination in newborns and infants. Methods: An analysis of the clinical data from 17 patients with cricopharyngeal incoordination who were admitted to the Department of Pediatrics, Pusan National University Hospital, between 2000 and 2006 was conducted retrospectively. The diagnosis of cricopharyngeal incoordination was established by the clinical characteristics and the videofluoroscopic swallowing studies. Results: The male to female ratio was 1๏ผ1.1 (males 8, females 9) the age range 1 to 60 days. The body weight of 11 patients (64.7%) was less than the 10th percentile at diagnosis. Six patients (35.3%) were born prematurely. The associated anomalies or diseases were chromosomal anomaly (2 cases), congenital heart disease (3 cases), and laryngomalacia, hypoxic brain damage or neonatal seizures (1 case each). The chief complaints of patients were recurrent aspiration pneumonia (10 cases), feeding difficulty (9 cases), dyspnea (4 cases), and chocking (4 cases). The severity of aspiration on the videoesophagogram or esophagogram was mild in 12 cases. The correlation between the severity of aspiration and the duration of tube feeding after the diagnosis was significant (p๏ผ0.05). Conclusion: Cricopharyngeal incoordination should be considered in the differential diagnosis of newborns and infants, without known risk factors associated with swallowing dysfunction, when they present with unexplained respiratory problems. Although the prognosis of cricopharyngeal incoordination is good, early diagnosis and tube feeding are recommended to prevent the complications associated with this disorder.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279496
|
oai_dc
|
์์์์ ๊ฒฐ์ ์ฑ ์์ผ์ผ๋ก ๋ฐํํ ์ ์ ๋ง์ฐ๊ด๋ฆผํ์กฐ์ง ๋ฆผํ์ข
1์
|
A Case of Gastric MALT Lymphoma Presenting as Nodular Gastritis in a Child
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ด๊ฑด์ก(์์ธ๋ํ๊ต); ๊ณ ์ฌ์ฑ(์์ธ๋ํ๊ต); ์์ ๊ธฐ(์์ธ๋ํ๊ต); ์ดํ์น(๋ถ๋น์์ธ๋ํ๊ต๋ณ์); ์ํ๋(์์ธ๋ํ๊ต)"
] |
Most cases of mucosa-associated lymphoid tissue (MALT) lymphoma occur in adults. MALT lymphoma is very rare in children. Helicobacter pylori (H. pylori) infection is known to be an important etiologic factor predisposing to the development of gastric MALT lymphoma. A 12-year-old girl was admitted because of intermittent abdominal pain occurring over the preceding 2 years. Nodular gastritis of the stomach was demonstrated on endoscopy. H. pylori infection was confirmed using the rapid urease test and histopathology. Histopathological examination of gastric biopsy specimens revealed lymphoepithelial lesions pathognomonic of MALT lymphoma, and immunohistochemical staining for CD20 was diffusely positive. Therefore, the patient was diagnosed with gastric MALT lymphoma. Clinical manifestations and histopathologic findings compatible with MALT lymphoma improved with the eradication of H. pylori infection. We report a case of primary gastric MALT lymphoma in a child, associated with H. pylori infection and presenting as nodular gastritis.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001279449
|
oai_dc
|
๋ณตํต์ด ์๋ ์์์ฒญ์๋
์์ ์๋์ผ์ ์ ๋ณ๋ฅ ๊ณผ ์ํ์ธ์
|
Prevalence and Risk Factors Associated with Esophagitis in Children with Abdominal Pain
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊ถํ์ (๊ฐ์ฒ์๊ณผ๋ํ๊ต); ์ด๋์ฉ(๊ฐ์ฒ์๊ณผ๋ํ๊ต); ์กฐ๊ฐํธ(๊ฐ์ฒ์๊ณผํ๋ํ๊ต); ์๋์ฐ(๊ฐ์ฒ์๊ณผํ๋ํ๊ต); ์ฐจํ(๊ฐ์ฒ์๊ณผ๋ํ๊ต); ๋ฅ์ผ(๊ฐ์ฒ์๊ณผํ๋ํ๊ต)"
] |
Purpose: Children with esophagitis express a variety of nonspecific symptoms and signs depending on their age, and diagnosis is limited because gastrointestinal endoscopy (GFS) and biopsy are difficult to perform. The aim of this study was to examine the prevalence of esophagitis in children with upper abdominal pain, to determine the necessity of esophageal biopsy, and to evaluate the associated risk factors.
Methods: We reviewed 266 pediatric patients with upper abdominal pain who underwent history-taking, physical examination, and GFS with esophageal and gastric biopsies between January 2006 and December 2007. Esophagitis was confirmed on biopsy. We analyzed the risk factors for histologic esophagitis and the necessity of esophageal biopsy.
Results: The prevalence of esophagitis was 19.9% (53/266 patients). The sensitivity and specificity of endoscopic diagnosis were 41.5% and 77%. Of 53 patients with histologic esophagitis, reflux esophagitis was seen in 50 patients, eosinophilic esophagitis was seen in 2 patients, and esophageal candidiasis was seen in 1 patient. Vomiting was a significant factor in patients under 8 yr of age (p๏ผ0.05). H. pylori infection was documented in 41.5% of patients with histologic esophagitis, compared with 58.5% of patients not infected with H. pylori (p๏ผ0.05). The possibility of histologic esophagitis was higher in patients with H. pylori infection (OR 2.5, 95% CI 1.2544 to 4.8286) and in those who visited in the spring (OR 2.5, 95% CI 1.2544 to 4.8286).
Conclusion: We believe esophageal tissue biopsy should be performed in pediatric patients with upper gastrointestinal symptoms who are undergoing GFS and stomach tissue biopsy, especially preschoolers and H. pylori-infected children in the spring
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001047116
|
oai_dc
|
์์ ๋์ฅ์์ ๋ฐ์ํ ์ ์ด์ฑ ๋ฐ์ง์ธํฌ์ 1์
|
A Case of Metastatic Signet Ring Cell Carcinoma ofthe Colon in a Child
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ค๋์ฑ(์์ธ๋ํ๊ต); ํ๊ฒฝํฌ(์์ธ๋ํ๊ต); ์ ์ง์ฐ(์์ธ๋ํ๊ต); ์ฌ์ ์ฅ(์์ธ๋ํ๊ต); ๋ฐ์ง์(์์ธ๋ํ๊ต); ์ํ๋(์์ธ๋ํ๊ต); ๊ณ ์ฌ์ฑ(์์ธ๋ํ๊ต); ์ ํฌ์(์์ธ๋ํ๊ต); ์ํจ์ญ(์์ธ๋ํ๊ต); ๋ฐ๊ท์(์์ธ๋ํ๊ต); ๊ฐ๊ฒฝํ(์์ธ๋ํ๊ต); ์ฒ์ ์(์์ธ๋ํ๊ต); ๊น์ฐ์ (์์ธ๋ํ๊ต); ์์ ๊ธฐ(์์ธ๋ํ๊ต)"
] |
์์์์์ ์ฅ๊ด๊ณ ์
์ฑ ์ข
์ ํนํ, ๋์ฅ์์ ๊ทนํ ๋๋ฌธ ์งํ์ด๋ค. ๊ทธ๋ฌ๋, ๋์ฅ์ ์์ ์ฅ๊ด๊ณ ์ํผ์ธํฌ์์ด ๊ฐ์ฅ ํธ๋ฐํ๋ ๋ถ์์ด๋ฉฐ, ๋ฐ์ง์ธํฌ์์ ์ฑ์ธ๊ณผ๋ ๋ฌ๋ฆฌ ์์ ๋์ฅ์ ์ค์์ ๊ฐ์ฅ ํํ ์กฐ์งํํ ์ค ํ๋์ด๋ค. ๊ตญ๋ด์์๋ ์์ ๋์ฅ์์ ๋ฐ์ํ ๋ฐ์ง์ธํฌ์์ ๋ํ ๋ณด๊ณ ๋ ์์ง ์์๋ค. ๋ฐ์ง์ธํฌ์์ ์ ์ก์ด ์ธํฌ ๋ด์ ํ๋ถํ๊ณ ํต์ด ํ์ชฝ์ผ๋ก ์น์ฐ์ณ ์๋ ํน์ง์ ๊ณ ๋ฆฌ ๋ชจ์์ ์ ์ธํฌ๊ฐ ์ ์ฒด ์ ์ธํฌ์ 50% ์ด์์ ์ฐจ์งํ๋ ์กฐ์ง ์๊ฒฌ์ผ๋ก ์ง๋จ๋๋ค. ์ ์๋ค์ ๋ณตํต, ์ฒด์ค๊ฐ์, ์ํต, ์ข์ธก ๋ํด๋ถ ํต์ฆ, ํ๋ณ์ผ๋ก ๋ด์ํ 11์ธ ๋จ์์์ ๋ด์๊ฒฝ ์กฐ์ง๊ฒ์ฌ ์๊ฒฌ์ผ๋ก ํ์ง๋ ๋ณต๊ฐ๋ด ์นจ์ต, ํ์ก ๋ฐ ๋ฆผํ์ฑ ์ ์ด๊ฐ ์งํ๋ ์์ ๋์ฅ์์์ ์ ์ด์ฑ ๋ฐ์ง์ธํฌ์์ ๊ฒฝํํ์๊ธฐ์ ๋ณด๊ณ ํ๋ ๋ฐ์ด๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001047111
|
oai_dc
|
์์์์ ๋จ์ ๋ณต๋ถ X-์ ์ฌ์ง์ผ๋ก ๋ณ๋น๋ฅผ ์ง๋จํ๋๋ฐ ์์ด Barr, Blethyn๊ณผ Leech ์ ์์ฒด๊ณ์ ์ ํ๋
|
The Accuracy of Barr, Blethyn and Leech Scoring Systems onPlain Abdominal Radiographs in Childhood Constipation
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋ฌธ์ง์(์กฐ์ ๋ํ๊ต); ๋ฌธ๊ฒฝ๋(์กฐ์ ๋ํ๊ต)"
] |
๋ชฉ ์ : ์์์์ ๊ธฐ๋ฅ์ฑ ๋ณ๋น๋ ์ํ๊ธฐ ์ฆ์ ์ค ๊ฐ์ฅ ํํ ์ฆ์์ด๋ ๊ฐ ๊ฐ์ธ์ด ํธ์ํ๋ ์ฆ์์ด ๋ค์ํ์ฌ ์ฝ๊ฒ ์ ์ํ๊ธฐ ์ด๋ ต๋ค. ๋จ์ ๋ณต๋ถ X-์ ์ฌ์ง์ ์ด์ฉํ ์ ์์ฒด๊ณ(scoring system)๋ ๊ฐ๋จํ๊ณ ๋น์ฉ์ด ์ ๊ฒ ๋ค์ด ๋ณ๋น์ ์ ๋๋ฅผ ํ๊ฐํ๋๋ฐ ์ฌ์ฉํ๊ณ ์๋ค. ๊ทธ๋ฌ๋ ์์ ๋ณ๋น์ ์ ๋๋ฅผ ํ๊ฐํ๋๋ฐ ์ด๋ค ์ ์์ฒด๊ณ๊ฐ ์์์ ์ผ๋ก ๋ ์ ์ฉํ์ง์ ๋ํ ์ฐ๊ตฌ๋ ๋งค์ฐ ๋๋ฌผ๋ค. ๋ฐ๋ผ์ ์ ์๋ค์ ์์ ๋ณ๋น ํ์์์ ๋จ์ ๋ณต๋ถ ๋ฐฉ์ฌ์ ์ฌ์ง์ ์ด์ฉํ์ฌ Barr, Blethyn๊ณผ Leech ์ ์๋ฅผ ์ธก์ ํ์ฌ ์ ์ฉ์ฑ์ ๋น๊ต ์ฐ๊ตฌํ์๋ค.๋ฐฉ ๋ฒ: 2006๋
1์๋ถํฐ 8์๊น์ง ์กฐ์ ๋ํ๊ต ๋ณ์ ์์๊ณผ ์ธ๋๋ฅผ ๋ฐฉ๋ฌธํ๊ฑฐ๋ ์
์ํ 4์ธ์์ 15์ธ ์ฌ์ด์ ํ์ 77๋ช
(๋ณ๋น๊ตฐ 38๋ช
, ๋์กฐ๊ตฐ 39๋ช
)์ ๋์์ผ๋ก ํ์๋ค. ๋ค ๋ช
์ ์ ๊ณต์๊ฐ 77๋งค์ ๋์ผํ ๋จ์ ๋ณต๋ถ X-์ ์ฌ์ง์ ๋ณด๊ณ Barr, Blethyn๊ณผ Leech ์ ์์ฒด๊ณ๋ฅผ ์ฌ์ฉํ์ฌ 1์ฃผ ๊ฐ๊ฒฉ์ผ๋ก ๊ฐ๊ฐ 2ํ ์ ์๋ฅผ ๋งค๊ฒผ์ผ๋ฉฐ ์ ์ ์ธก์ ์์ ํ์์ ๋ํ ์ฌ์ ์ ๋ณด๋ฅผ ๋ฐฐ์ ํ์๋ค. ๊ฐ ์ ์์ฒด๊ณ ๋ฐฉ๋ฒ์ ๋ํ ๊ฒ์ฌ์๋ค์ ์ ์์ฑ์ ฮบ ์์์ ๊ณ์ฐํ์ฌ ํ๊ฐํ์๋ค.๊ฒฐ ๊ณผ: ๋์์ 77๋ช
์ค ๋จ์๋ 41๋ช
(53.2%), ์ฌ์๋ 36๋ช
(46.8%)์ด์๊ณ ๋ณ๋น๊ตฐ์ 38๋ช
(49.4%), ๋์กฐ๊ตฐ์ 39๋ช
(50.6 %)์ด์๋ค. ๋ค ๋ช
์ ๊ฒ์ฌ์๊ฐ ์ธก์ ํ Barr ์ ์๋ก ๊ณ์ฐํ ฮบ ์์๋ ๊ฐ๊ฐ 0.75, 0.66, 0.68, 0.71์ด์๊ณ , Blethyn ์ ์๋ก ๊ณ์ฐํ ฮบ ์์๋ 0.61, 0.58, 0.55, 0.63์ด๋ฉฐ, Leech ์ ์๋ก ๊ณ์ฐํ ฮบ ์์๋ 0.88, 0.92, 0.86, 0.89์ด์๋ค. Barr ์ ์๋ก ๊ณ์ฐํ ฮบ ์์๋ ์ฒซ ๋ฒ์งธ ์ธก์ ์์ ๊ฐ๊ฐ 0.66, 0.67, 0.69, 0.66์ด์์ผ๋ฉฐ, 1์ฃผ ํ์ ๋ ๋ฒ์งธ ์ธก์ ์์๋ ๊ฐ๊ฐ 0.68, 0.65, 0.71, 0.68๋ก ์ธก์ ์๊ธฐ์ ๋ฐ๋ผ ์ ์ํ ์ฐจ์ด๊ฐ ์์๋ค(p๏ผ0.05)(Fig. 1). ๋ค๋ช
์ ๊ฒ์ฌ์๊ฐ ์ธก์ ํ Blethyn ์ ์๋ก ๊ณ์ฐํ ฮบ ์์๋ ์ฒซ ๋ฒ์งธ ์ธก์ ์์ ๊ฐ๊ฐ 0.44, 0.55, 0.48, 0.33์ด์์ผ๋ฉฐ, 1์ฃผ ํ์ ๋ ๋ฒ์งธ ์ธก์ ์์๋ 0.65, 0.34, 0.39, 0.46์ผ๋ก ์ธก์ ์๊ธฐ์ ๋ฐ๋ผ ์ ์ํ ์ฐจ์ด๊ฐ ์์์ผ๋ฉฐ(p๏ผ0.05), Leech ์ ์๋ก ๊ณ์ฐํ ฮบ ์์๋ ์ฒซ ๋ฒ์งธ ์ธก์ ์์ ๊ฐ๊ฐ 0.88, 0.91, 0.92, 0.86์ด๊ณ ๋ ๋ฒ์งธ ์ธก์ ์์ ๊ฐ๊ฐ 0.81, 0.88, 0.89, 0.84๋ก ์ธก์ ์๊ธฐ์ ๋ฐ๋ผ ์ ์ํ ์ฐจ์ด๊ฐ ์์๋ค(p๏ผ0.05). Barr ์ ์์ ํ๊ท ์น๋ ๋ณ๋น๊ตฐ์ 9.68ยฑ3.55, ๋์กฐ๊ตฐ์ 5.32ยฑ3.45๋ก ๋ ๊ตฐ ์ฌ์ด์ ์ ์ํ ์ฐจ์ด๊ฐ ์์๋ค(p๏ผ0.05). Leech ์ ์์ ํ๊ท ์น๋ ๋ณ๋น๊ตฐ์ 10.42ยฑ3.12, ๋์กฐ๊ตฐ์ 6.28ยฑ3.56์ผ๋ก ๋ ๊ตฐ ์ฌ์ด์ ์ ์ํ ์ฐจ์ด๊ฐ ์์๋ค(p๏ผ0.05). ๋ค ๋ช
์ ๊ฒ์ฌ์๊ฐ ์ธก์ ํ Barr ์ ์์ ํน์ด๋๋ ๊ฐ๊ฐ 0.51, 0.55, 0.54, 0.71์ด์๊ณ ๋ฏผ๊ฐ๋๋ ๊ฐ๊ฐ 0.68, 0.61, 0.69, 0.61์ด์๋ค. Leech ์ ์์ ํน์ด๋๋ ๊ฐ๊ฐ 0.88, 0.91, 0.92, 0.86์ด์๊ณ ๋ฏผ๊ฐ๋๋ ๊ฐ๊ฐ 0.90, 0.89, 0.91, 0.84์๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001047118
|
oai_dc
|
์์ ์ง์ฅ ์ ์์ข
1์
|
A Case of Rectal Carcinoid Tumor in a Child
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊ฐ์ํ(๋ถ์ฐ์ฑ๋ชจ๋ณ์); ์ํ์ด(๋ถ์ฐ์ฑ๋ชจ๋ณ์); ๊น์ฌ์(์ถฉ๋จ๋ํ๊ต)"
] |
์ ์๋ค์ ๋ด์ 1๋
์ ๋ถํฐ ๊ฐํ์ ์ธ ๋ณตํต๊ณผ ํจ๊ป ๋ณตํต ์์ ํญ์ ๋๋ฐ๋๋ ์๋์ ๋นํน์ด์ ์ธ ์ค์ฌ๊ฐ ๋ฐ๋ณต๋์ด ๋ด์ํ 13์ธ ๋จ์์์ ์ง์ฅ ์ ์์ข
์ ์ง๋จํ๊ณ ๋ด์๊ฒฝ์ ์ ์ ์ ๋ก ์น๋ฃํ ์ฆ๋ก๋ฅผ ๊ฒฝํํ์๊ธฐ์ ๋ฌธํ ๊ณ ์ฐฐ๊ณผ ํจ๊ป ๋ณด๊ณ ํ๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001044734
|
oai_dc
|
์ผ๊ฐ ๋ํ๋ณ์์์์ ์์ ์์ฅ๊ด ๋ด์๊ฒฝ ์์ ์์ต๊ทผ ๊ฒฝํ
|
Changes in Pediatric Gastrointestinal Endoscopy:Review of a Recent Hospital Experience
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋ฐ๊ฒฝํฌ(๋ถ์ฐ๋ํ๊ต); ๋ฐ์ฌํ(๋ถ์ฐ๋ํ๊ต)"
] |
๋ชฉ ์ : ์์์์ ์์ฅ๊ด ๋ด์๊ฒฝ ์์ ์ด ๋น์ฝ์ ์ผ๋ก ๋๊ณ ์๊ณ ๋ด์๊ฒฝ ๊ธฐ์ ๊ณผ ์ ์์ฆ์ด ํ๋๋๊ณ ์์ผ๋ ์ด๋ฌํ ๋ณํ๋ฅผ ๋ถ์ํ ๋ณด๊ณ ๊ฐ ๋งค์ฐ ๋๋ฌผ์ด ํ ๋ณ์์์ ์ต๊ทผ ์ํ๋ ์์ฅ๊ด ๋ด์๊ฒฝ ๊ฒ์ฌ์ ๊ฒฝํ์ ๋ถ์ํจ์ผ๋ก์จ ์์์์ ์์ฅ๊ด ๋ด์๊ฒฝ ๊ฒ์ฌ์ ์ ์ฉ์ฑ๊ณผ ์์ ์ฑ์ ์ดํด๋ณด์๋ค.๋ฐฉ ๋ฒ: 2001๋
1์๋ถํฐ 2005๋
6์๊น์ง 4๋
6๊ฐ์ ๋์ ๋ถ์ฐ๋ํ๊ต๋ณ์ ์์๊ณผ์์ ์์ฅ๊ด ๋ด์๊ฒฝ ๊ฒ์ฌ๋ฅผ ๋ฐ์๋ 1,040๋ช
์ ํ์๋ฅผ ๋์์ผ๋ก ๋ณ๋ ฅ์ง ๋ถ์์ ํตํ ํํฅ์ ์ฐ๊ตฌ๋ฅผ ์ํํ์๋ค. ์ด 1,040์์ ๋ด์๊ฒฝ ๊ฒ์ฌ๊ฐ ์ํ๋์๊ณ ์๋ถ ์์ฅ๊ด ๊ฒ์ฌ๊ฐ 840์, ํ๋ถ ์์ฅ๊ด ๊ฒ์ฌ๊ฐ 200์์๋ค. ๊ฒฐ ๊ณผ: ํ์์ ๋จ๋
๋น๋ 1.25๏ผ1์ด์๋ค. ํ์์ ํ๊ท ์ฐ๋ น์ด 8.5ยฑ2.1์ธ์๊ณ ์ ์์์ ์์๊ฐ 6.0%๋ฅผ ์ฐจ์งํ์์ผ๋ฉฐ 5์ธ ์ดํ๊ฐ ์ ๋ฐ์ ์ฐจ์งํ์๋ค. ์๋ถ ์์ฅ๊ด(UGI) ๋ฐ ํ๋ถ ์์ฅ๊ด(LGI)์ ์ง๋จ์ ๋ด์๊ฒฝ ๊ฒ์ฌ๋ ๊ฐ๊ฐ 634๋ช
๊ณผ 163๋ช
์์ ์ํ๋์๋ค. UGI ๊ฒ์ฌ์ ์ฃผ๋ ์ ์์ฆ์ ๋ณตํต(38.8%), ๊ตฌํ (19.4%), ์ด๋ฌผ(17.7%), ํ ํ(10.3%) ๋ฑ์ด์๊ณ , LGI ๊ฒ์ฌ์ ์ฃผ๋ ์ ์์ฆ์ ํ๋ณ(56.0%), ๋ณตํต(27.5%), ์ค์ฌ(3.0%) ๋ฑ์ด์๋ค. UGI ์น๋ฃ์ ๋ด์๊ฒฝ์ ์ ์ข
๋ฅ๋ก๋ ์ด๋ฌผ ์ ๊ฑฐ(148์), ์๋ ํ์ฐฉ์ ๋ํ ํ์ ํ์ฅ์ (27์), ๊ฒฝํผ ๋ด์๊ฒฝํ ์๋ฃจ์ (15์), ๋ด์๊ฒฝ์ ์๋ ์ ๋งฅ๋ฅ ๊ฒฐ์ฐฐ์ (3์)์ด ์์๋ค. LGI ์น๋ฃ์ ๋ด์๊ฒฝ์ ์ 37๋ช
์์ ์ํ๋์์ผ๋ฉฐ ์ฉ์ข
์ ์ ์ ์ด 34์, ์๋ฅด๊ณค ํ๋ผ์ฆ๋ง ์๊ณ ์ ์ด 3์์๋ค. ๋ด์๊ฒฝ์ ์ ํฉ๋ณ์ฆ์ผ๋ก ์๋, ์, ๋์ฅ์ ์ฒ๊ณต์ด ๊ฐ๊ฐ 1์์ฉ ์์๊ณ , ํธํก ๊ณค๋์ด 4์์์ ๋ฐ์ํ์๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001047120
|
oai_dc
|
์์์์ ๋๋ง ์ผ์ถ์ก์ ๋๋ฐํ ์ธ์์ฑ ์ท์ฅ ์ ๋จ ๋ฐ์ท์ฅ ์ฃผ๊ด ์์ 1์
|
A Case of Traumatic Pancreatic Transection with Main DuctDisruption and Pleural Effusion in a Child
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ด๊ฐ์ฐ(์ฑ๊ท ๊ด๋ํ๊ต); ์ ํ์(์ฑ๊ท ๊ด๋ํ๊ต); ์ด์งํ(ํ๋ฆผ๋ํ๊ต); ์ต์ฐํธ(์ฑ๊ท ๊ด๋ํ๊ต); ํ์ง์(์ฑ๊ท ๊ด๋ํ๊ต)"
] |
์ท์ฅ ์์์ ์์์์๋ ํํ์ง ์์ผ๋ฉฐ ์์ ์ฆ์๊ณผ ์ดํ์ ์๊ฒฌ์ด ๋๋ ทํ์ง ์์ ์ง๋จ์ด ์ด๋ ค์ด ๊ฒฝ์ฐ๊ฐ ๋ง์๋ฐ ์์ ์ ๋์ ์์น์ ๋ํ ์ ํํ ํ๊ฐ๋ฅผ ๋ฐํ์ผ๋ก ์น๋ฃ๊ฐ ์ง์ฐ๋์ง ์๋๋ก ํ์ฌ ํฉ๋ณ์ฆ ๋ฐ์์ ๋ง๋๋ก ํด์ผ ํ ๊ฒ์ด๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001044735
|
oai_dc
|
์์๊ณผ ์์ฌ์ ์ํด ์ํ๋ ๋ณต๋ถ ์ด์ํ ๊ฒ์ฌ1,000์์ ๋ํ ๋ถ์
|
Analysis of 1,000 Cases of Abdominal UltrasonographyPerformed by a Pediatrician
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋ฐฐ์์ธ(๋ถ์ฐ๋ํ๊ต); ๋ฐ์ฌํ(๋ถ์ฐ๋ํ๊ต)"
] |
๋ชฉ ์ : ์์์์ ์ด์ํ ๊ฒ์ฌ๋ ๋ณต๋ถ ์งํ์ ์ง๋จ์ ์ค์ํ ์ญํ ์ ํ๋ค. ์์์ ํน์ฑ์ ์ ์๊ณ ์๋ ์์๊ณผ ์์ฌ์ ์ํด ์ํ๋ ๋ณต๋ถ ์ด์ํ ๊ฒ์ฌ์ ๊ฒฝํ์ ๋ถ์ํ์๋ค.๋ฐฉ ๋ฒ: 2003๋
1์๋ถํฐ 2005๋
6์๊น์ง ๋ถ์ฐ๋ํ๊ต๋ณ์ ์์๊ณผ์์ ๋ณต๋ถ ์งํ์ ์ฆ์์ผ๋ก ๋ด์ํ์ฌ ๋ณต๋ถ ์ด์ํ ๊ฒ์ฌ๋ฅผ ๋ฐ์๋ 1,000๋ช
์ ํ์๋ฅผ ๋์์ผ๋ก ๋ณ๋ ฅ์ง์ ์ด์ํ ๊ฒ์ฌ ์๊ฒฌ์ ํํฅ์ ์ผ๋ก ๋ถ์ํ์๋ค. ์ด์ํ ๊ฒ์ฌ๋ 1๋ช
์ ์์๊ณผ ์์ฌ์ ์ํด ์ํ๋์์ผ๋ฉฐ ์ด์ํ ๊ธฐ๊ธฐ๋ Sequoia System์ ์ด์ฉํ๊ณ 3์ข
๋ฅ์ ํ์ด์๋ฅผ ์ฌ์ฉํ์๋ค.๊ฒฐ ๊ณผ: ๋จ์๊ฐ 584๋ช
(58.4%), ์ฌ์๊ฐ 416๋ช
(41.6%)์ด์๊ณ , ํ๊ท ์ฐ๋ น์ 4.7ยฑ4.0์ธ์๋ค. 1์ธ ๋ฏธ๋ง์ด 274๋ช
(27.4%), 1โผ5์ธ๊ฐ 310๋ช
(31.0%), 6โผ10์ธ๊ฐ 267๋ช
(26.7%), 11์ธ ์ด์์ด 149๋ช
(14.9%)์ด์๋ค. ๋ด์ ์ ์ฃผ์ฆ์์ ๋ณตํต์ด 439๋ช
(43.9%)์ผ๋ก ๊ฐ์ฅ ๋ง์๊ณ , ๊ตฌํ , ๊ฐ ํจ์์น์ ์ฆ๊ฐ, ํฉ๋ฌ, ์ค์ฌ, ๋ณต๋ถํฝ๋ง ๋ฑ์ด ์์๋ค. ๊ฒ์ฌ ๊ฒฐ๊ณผ ์ ์ ์๊ฒฌ์ด 421๋ช
(42.1%), ๋น์ ์ ์๊ฒฌ์ด 579๋ช
(57.9%)์ด์๋ค. ๋น์ ์ ์๊ฒฌ์ผ๋ก๋ ์ฅ๊ฐ๋ง ๋ฆผํ์ ์ผ์ด 182๋ช
(31.5%)์ผ๋ก ๊ฐ์ฅ ๋ง์๊ณ , ๊ทธ ์ธ ์ง๋ฐฉ๊ฐ, ๊ฐ์ผ, ๊ฐ๋น์ข
๋, ์ฅ์ค์ฒฉ์ฆ ๋ฑ์ด ์์๋ค. ๋ณตํต์ผ๋ก ๊ฒ์ฌํ ๊ฒฝ์ฐ๋ ์ฅ๊ฐ๋ง ๋ฆผํ์ ์ผ์ด 32.6%๋ก ๊ฐ์ฅ ๋ง์๊ณ , ๊ทธ ์ธ ์ฅ์ค์ฒฉ์ฆ, ๊ธ์ฑ ์ถฉ์๋๊ธฐ์ผ, ์๋ก๊ฒฐ์, ๊ธ์ฑ ์ท์ฅ์ผ, ๋ด์ ๋ฑ์ด ์์๋ค. ๊ตฌํ ๋ก ๊ฒ์ฌํ ๊ฒฝ์ฐ๋ ์ฅ๊ฐ๋ง ๋ฆผํ์ ์ผ์ด 12.7%๋ช
์ผ๋ก ๊ฐ์ฅ ๋ง์๊ณ , ๊ทธ ์ธ ํน๋ฐ์ฑ ์ ๋ฌธ ํ์ฐฉ์ฆ, ๊ธ์ฑ ์ถฉ์๋๊ธฐ์ผ, ์ฅํ์์ฆ ๋ฑ์ด ์์๋ค. ๊ฐํจ์์น ์์น์ผ๋ก ๊ฒ์ฌํ ๊ฒฝ์ฐ๋ ์ง๋ฐฉ๊ฐ์ด 30๋ช
(25.4%)์ผ๋ก ๊ฐ์ฅ ๋ง์๊ณ , ๊ทธ ์ธ ๊ฐ์ผ, ์ด ๋ด๊ด๋ญ, ๊ฐ์ธ ๋ด๋ ํ์, ๊ฐ๊ฒฝ๋ณ์ฆ ๋ฑ์ด ์์๋ค. ๋น๋จ์์๊ณ ์งํ๊ณผ ๊ด๋ จ๋ 55์์ ์ด์ํ ๊ฒ์ฌ ์๊ฒฌ ์ค์์๋ ์์ ์ฆ์ด 25๋ช
(45.4%)์ผ๋ก ๊ฐ์ฅ ๋ง์๊ณ ์ ๊ฒฐ์, ๋ญ์ข
์ฑ ์ ์งํ, ์ข
์ ๋ฑ์ด ์์๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001044733
|
oai_dc
|
Henoch-Sch๏ผnlein ์๋ฐ์ฆ์์ Tumor NecrosisFactor-ฮฑ ์ ์ ์ ๋คํ์ฑ ๋ถ์
|
Analysis of the Tumor Necrosis Factor-ฮฑ Promoter Polymorphismin Children with Henoch-Sch๏ผnlein Purpura
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ํ๋(์์ธ๋ํ๊ต); ๊ณ ์ฌ์ฑ(์์ธ๋ํ๊ต); ์์ ๊ธฐ(์์ธ๋ํ๊ต)"
] |
๋ชฉ ์ : ๋ณธ ์ฐ๊ตฌ์์๋ Henoch-Schnlein ์๋ฐ์ฆ์ผ๋ก ์ง๋จ๋ ํ์๋ค์์ ๊ธ์ฑ๊ธฐ์ ๊ดํด๊ธฐ์ TNF-ฮฑ ๋๋๋ฅผ ์ธก์ ํจ์ผ๋ก์จ Henoch-Schnlein ์๋ฐ์ฆ์ ๋ฐ๋ณ๊ณผ ์์์์์ ๋ฐํ์ ์์ด TNF-ฮฑ์ ์์๋ฅผ ํ๊ฐํ๊ณ , ๊ฐ ํ์์์ TNF-ฮฑ 308, 238 ์ ์ ์ ๋คํ์ฑ์ ์ ์ ์ํ๊ณผ ๋๋ฆฝ์ ์ ์ ๋น๋๋ฅผ ๋ถ์ํจ์ผ๋ก์จ Henoch-Schnlein ์๋ฐ์ฆ์ ๋ฐ๋ณ์ ์์ด TNF-ฮฑ ์ ์ ์ ๋คํ์ฑ์ด ๊ฐ๋ ์์๋ฅผ ์์๋ณด๊ณ ์ ํ์๋ค.๋ฐฉ ๋ฒ: 2004๋
3์์์ 2005๋
11์๊น์ง ์์ธ๋๋ณ์ ๋ฐ ๋ถ๋น์์ธ๋๋ณ์ ์์๊ณผ์ ๋ด์ํ์ฌ Henoch-Schnlein ์๋ฐ์ฆ์ผ๋ก ์ง๋จ๋ฐ์ 40๋ช
์ ์์ ํ์๋ฅผ ๋์์ผ๋ก ํ์๊ณ , ๊ฑด๊ฐํ ์์ ํ์ 32๋ช
์ ๋์กฐ๊ตฐ์ผ๋ก ํ์๋ค. ํํฅ์ ์ธ ์๋ฌด๊ธฐ๋ก์ง ๊ฒํ ๋ฅผ ํตํด ํ์๋ค์ ์์์์์ ์กฐ์ฌํ์ฌ ์์ ์ ์๋ฅผ ํ๊ฐํ์๋ค. ํ์๊ตฐ์์ ๊ธ์ฑ๊ธฐ์ ๊ดํด๊ธฐ์ ํ์ฒญ TNF-ฮฑ ๋๋๋ฅผ ์ธก์ ํ์๋ค. ํ์๊ตฐ๊ณผ ๋์กฐ๊ตฐ์์ ํ์ก์ ์ฑ์ทจํ์ฌ TNF-ฮฑ 308๊ณผ 238 ์ ์ ์ ๋คํ์ฑ์ ์กฐ์ฌํ์๋ค.๊ฒฐ ๊ณผ: Henoch-Schnlein ์๋ฐ์ฆ์ผ๋ก ์ง๋จ๋ 40๋ช
(๋จ์ 20๋ช
, ์ฌ์ 20๋ช
)์ ํ์์์ ๊ธ์ฑ๊ธฐ์ ์ธก์ ํ ํ์ฒญ TNF-ฮฑ ๋๋๋ 23.17ยฑ11.31 pg/mL์์ผ๋ฉฐ, ์ฆ์ธ๊ฐ ์์ค๋ ํ์ ์ธก์ ํ ํ์ฒญ TNF-ฮฑ ๋๋๋ 10.56ยฑ 5.59 pg/mL๋ก์ ์ ์ํ๊ฒ ๊ฐ์ํ์๋ค(p=0.000). ํ์ฒญ TNF-ฮฑ์ Henoch-Schnlein ์๋ฐ์ฆ์ ์์ ์ ์ ๊ฐ์ ์ ์ํ ์๊ด๊ด๊ณ๋ ์์๋ค(r=0.310, p=0.070). TNF-ฮฑ 308 ์ ์ ์ํ ๋น๋๋ ํ์๊ตฐ์์ GG 80%, GA 20%์์ผ๋ฉฐ, ๋์กฐ๊ตฐ์์๋ GG 93.8%, GA 6.2%๋ก์ ํ์๊ตฐ์์ ๋์ GA ์ ์ ์ํ์ ๋น๋๋ฅผ ๋ณด์์ง๋ง ํต๊ณ์ ์ธ ์ ์์ฑ์ ์์๋ค(P=0.094). TNF-ฮฑ 238 ์ ์ ์ํ ๋ถํฌ๋ ํ์๊ตฐ์์ GG 97.5%, GA 2.5%์์ผ๋ฉฐ, ๋์กฐ๊ตฐ์์๋ GG 93.8%, GA 6.3%๋ก์ ๋ ๊ตฐ ์ฌ์ด์ ํต๊ณ์ ์ธ ์ ์์ฑ์ด ์์๋ค(p=0.429).
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001047110
|
oai_dc
|
์์ ๊ธ์ฑ ์ถฉ์์ผ์์ ๋ณต๋ถ์ด์ํ ์ดํ์ ์ฐํ๋จ์ธต์ดฌ์ ์ถ์ ๊ฒ์ฌ์ ์์์ ์์
|
Clinical Significance of Follow-up CT after Ultrasonographyfor Acute Appendicitis in Children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ ์ฑ๊ทผ(์ธ์ ๋ํ๊ต); ๋ฌธ์ง์(์ธ์ ๋ํ๊ต); ๊น๋จํฌ(์ธ์ ๋ํ๊ต); ํฉ์ข
ํฌ(์ธ์ ๋ํ๊ต); ๋จ์น์ฐ(์ธ์ ๋ํ๊ต); ๊น๋์ฑ(์ธ์ ๋ํ๊ต); ์ด์ข
๊ตญ(์ธ์ ๋ํ๊ต); ์์ ์ฑ(์ธ์ ๋ํ๊ต); ํํ๊ธธ(์ธ์ ๋ํ๊ต)"
] |
๋ชฉ ์ : ๊ธ์ฑ ์ถฉ์์ผ์ ๊ฐ์ฅ ํํ ์ธ๊ณผ์ ๋ณต๋ถ์งํ์ผ๋ก ๋์ด๊ฐ ์ด๋ฆด์๋ก ์กฐ๊ธฐ์ ์ฒ๊ณต์ด ๋ฐ์ํ๊ณ ์ง๋จ์ด ์ด๋ ต๋ค. ์ด์ ์ ์๋ค์ ๊ธ์ฑ ์ถฉ์์ผ์ ์ง๋จ์ ์์ด ์ด์ํ์ ์ ์ฐํ๋จ์ธต์ดฌ์(CT) ๋ฐ ์ด์ํ ์ดํ CT ์ถ์ ๊ฒ์ฌ์ ์์์ ์์๋ฅผ ์์๋ณด๊ณ ์ ํ์๋ค.๋ฐฉ ๋ฒ: 2002๋
3์๋ถํฐ 2006๋
2์๊น์ง ๊ธ์ฑ ๋ณต์ฆ์ผ๋ก ์ผ์ฐ๋ฐฑ๋ณ์ ์์๊ณผ์ ์ธ๊ณผ์ ๋ด์ํ 16์ธ ๋ฏธ๋ง์ ํ์ ์ค ๊ธ์ฑ ์ถฉ์์ผ์ผ๋ก ์ง๋จ๋์ด ์ถฉ์์ ์ ์ ์ ์ํ ๋ฐ์ 419๋ช
์ ๋์์ผ๋ก ํ์๋ค. ์ด์ํ์ CT ๊ฐ๊ฐ์ ๋ฏผ๊ฐ๋, ํน์ด๋, ์์ฑ์์ธก์น, ์์ฑ์์ธก์น๋ฅผ ์ฐ์ถํ์๊ณ , ์ด์ํ ํ CT ์ถ์ ๊ฒ์ฌ ์ฌ์ด์ ์๊ฐ ๊ฐ๊ฒฉ๊ณผ ํญ์์ ์ฌ์ฉ ๊ธฐ๊ฐ, ์
์ ๊ธฐ๊ฐ ๋ฑ ์์ ๊ฒฝ๊ณผ์ ๋ํด ๋ฏธ์น๋ ์ํฅ์ ์กฐ์ฌํ์๋ค.๊ฒฐ ๊ณผ: ๋์ ํ์๋ ๋จ์๊ฐ 260๋ช
(61.9%), ์ฌ์๊ฐ 159๋ช
(38.1%)์ผ๋ก ์ฑ๋น๋ 1.63๏ผ1์ด์๋ค. ์์ ๊ฒฐ๊ณผ๋ก ์ฒ๊ณต๋ฅ ์ 42.4% (167๋ช
)์ด์๋ค. ๊ฒ์ฌ์ ๋ฏผ๊ฐ๋, ํน์ด๋, ์์ฑ์์ธก์น, ์์ฑ์์ธก์น๋ ์ด์ํ์ ๊ฒฝ์ฐ ๋น์ฒ๊ณต์ฑ ์ถฉ์์ผ์์ 98.7%, 96.8%, 98.1%, 97.8%์ด์๊ณ , ์ฒ๊ณต์ฑ์์ 90.8%, 100%, 100%, 81.9%์๋ค. CT์ ๊ฒฝ์ฐ ๋น์ฒ๊ณต์ฑ์์ 96.4%, 100%, 100%, 96.5%์์ผ๋ฉฐ, ์ฒ๊ณต์ฑ์์ 86.6%, 100%, 100%, 87.5%์๋ค. ์ด์ํ ์ดํ CT๋ฅผ ์ค์ํ ๊ฒฝ์ฐ ๋น์ฒ๊ณต์ฑ์์ ๋ชจ๋ 100%, ์ฒ๊ณต์ฑ์์ 87.5%, 100%, 100%, 92.0%๋ฅผ ๋ณด์๋ค. ์ด์ํ ์ดํ CT๋ฅผ ์ํ ๋ฐ์ 9๋ช
์ ์ฒ๊ณต์ฑ ์ถฉ์์ผ ํ์ ์ค ๋ถ์ ๊ฐ๋ฅํ 7๋ช
์์ ์ด์ํ ์ดํ์ CT๋ฅผ ์ํํ๊ธฐ๊น์ง ์๊ฐ ๊ฐ๊ฒฉ๊ณผ ํญ์์ ์ฌ์ฉ ๊ธฐ๊ฐ(r=0.0472, p=0.019), ์ด ์
์ ๊ธฐ๊ฐ(r=0.0845, p=0.001)์ ์ ์ํ ์๊ด๊ด๊ณ๋ฅผ ๋ณด์๋ค. ๋ํ ๋ ๊ฒ์ฌ ๊ฐ์ ๊ฐ๊ฒฉ์ด 30์๊ฐ ์ด๋ด์ธ ๊ฒฝ์ฐ ๊ฒ์ฌ ๊ฐ์ ์๊ฐ ๊ฐ๊ฒฉ๊ณผ ์ด ํญ์์ ์ฌ์ฉ ๊ธฐ๊ฐ ๋ฐ ์ด ์
์๊ฒฝ๊ณผ ์ฌ์ด์ ์ ์ํ ์๊ด ๊ด๊ณ๋ ์์๋ค(p=0.084, p=0.153).
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001044732
|
oai_dc
|
์์ ๊ฐ์ด์์ ํ์ฌ
|
Current Status of Pediatric Liver Transplantation
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊น๊ฒฝ๋ชจ(์ธ์ฐ๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART001047112
|
oai_dc
|
์์ ๊ณจ๋ฐ์ ๊ทผ์ค์กฐ์์ ๋ฐ์ด์คํผ๋๋ฐฑ ์น๋ฃ์ ์ ์ฉ์ฑ
|
Assessment of the Effectiveness of Biofeedback Therapyin Children with Pelvic Floor Dyssynergia
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋ฐ๊ธฐ์(์ธ์ฐ๋ํ๊ต); ์ฅ์ํฌ(๋ถ๋น์ฌ์๋ณ์); ๊น๊ฒฝ๋ชจ(์ธ์ฐ๋ํ๊ต)"
] |
๋ชฉ ์ : ์ง์ฅ ํญ๋ฌธ๊ธฐ๋ฅ๊ฒ์ฌ๋ฒ์ ๋ฐ๋ฌ๋ก ์์ ๋ง์ฑ ๋ณ๋น ํ์ ์ค์์๋ ์ฑ์ธ์์์ ๋ง์ฐฌ๊ฐ์ง๋ก PFD๋ฅผ ๋ณด์ด๋ ๊ฒฝ์ฐ๊ฐ ์์์ด ์๋ ค์ง๊ณ ์๋ค. ํ์ง๋ง PFD ํ์์ ์น๋ฃ์ ์ฌ์ฉํ๋ BT๋ ์์์์๋ ํ์กฐ๊ฐ ์ด๋ ต๊ณ , ์์ ๋ณ๋น๋ ์ํธํ ์์ฐ๊ฒฝ๊ณผ๋ฅผ ๊ฐ์ง๋ค๋ ๋ณด์์ ์ธ ์ธ์์ผ๋ก ์ธํด ๋ณดํธ์ ์ผ๋ก๋ ์ํ๋์ง ์์๋ค. ์์ PFD์์์ BT์ ํจ์ฉ์ฑ์ ์์๋ณด๊ธฐ ์ํ์ฌ ์ด๋ฒ ์ฐ๊ตฌ๋ฅผ ์ํํ์๋ค.๋ฐฉ ๋ฒ: 2002๋
9์๋ถํฐ 2005๋
2์๊น์ง ๋ณ์ง๋ฆผ ๋๋ ๋ณด์กด ์น๋ฃ์ ์ ๋ฐ์ํ์ง ์๋ ๋ง์ฑ ๋ณ๋น๋ฅผ ์ฃผ์๋ก ์์ธ์์ฐ๋ณ์ ์์๊ณผ๋ก ์๋ขฐ๋ ํ์ ์ค ์ง์ฅ ํญ๋ฌธ๊ธฐ๋ฅ๊ฒ์ฌ์์ PFD๋ก ์ง๋จํ ํ์ 70๋ช
์ ๋์์ผ๋ก ํ์๋ค. ์ง๋จ์ ์ํ ์ง์ฅ ํญ๋ฌธ๊ธฐ๋ฅ๊ฒ์ฌ๋ก ๋ฐฐ๋ณ์กฐ์์ , ํญ๋ฌธ ์ง์ฅ๋ด์๊ฒ์ฌ, ๋ฐฐ๋ณ ๋์ ์ ๊ทผ์ ๋์ ํ์ ๋ฐฐ์ถ๊ฒ์ฌ ๋ฑ์ด ์ํ๋์๋ค. BT๋ ํญ๋ฌธ๋ด ๊ทผ์ ๋๋ฅผ ์ด์ฉํ์๊ณ , ์ฃผ 2โผ3ํ๋ฅผ ๊ธฐ๋ณธ์ผ๋ก ํ๋น 20๋ถ ์ ๋ ์ค์ํ์๋ค. ์น๋ฃ ์ข
๋ฃ ์์๋ ํ์ ๋ฐฐ์ถ๊ฒ์ฌ, ๋ฐฐ๋ณ ๋์ ์ ๊ทผ์ ๋๋ฅผ ์ค์ํ์๋ค. ์น๋ฃ ์ ํ์ Bristol ๋ถ๋ฅ์ ๋ฐ๋ฅธ ๋๋ณ ๋ชจ์๊ณผ ์ฃผ๋น ๋ฐฐ๋ณ ํ์, ๋ฐฐ๋ณ ์๊ฐ ๋ฑ์ ๋ณํ์ ์ฝ๋ฌผ ์น๋ฃ ์ค๋จ ์ฌ๋ถ ๋ฑ์ ๋ํด ์ค๋ฌธ์ผ๋ก ์กฐ์ฌํ์๋ค. ์น๋ฃ ์ข
๋ฃ 6๊ฐ์ ์ด์ ๊ฒฝ๊ณผ๋ ํ์๋ค์ ๋์์ผ๋ก ํ์ฌ์ ๋ฐฐ๋ณ ์ํ์ ๋ํด ์ ํ ์ค๋ฌธ์ ์ํํ์๋ค. ๋ํ PFDํ์ ์ค BT๋ฅผ ๊ฑฐ๋ถํ๋ ํ์๋ค์ ๋์กฐ๊ตฐ์ผ๋ก ํ์ฌ BT์ ํจ๊ณผ๋ฅผ ์์๋ณด์๋ค.๊ฒฐ ๊ณผ: BT ์น๋ฃ ์ ๊ณผ ๋น๊ตํ์ฌ ์น๋ฃ ์งํ์ ์ฃผ๋น ๋ฐฐ๋ณ ํ์, ๋ณ์ ๋ชจ์, ๋ฐฐ๋ณ ์๊ฐ ๋ฑ์ ์ฆ์๊ณผ ํญ๋ฌธ๋ด ๊ทผ์ ๋, ํ์ ๋ฐฐ์ถ๊ฒ์ฌ ๋ฑ์ ๊ฒฐ๊ณผ๋ ๋ชจ๋ ์ ์ํ ํธ์ ์ ๋ณด์๋ค. ํ๊ท ์ฝ 20๊ฐ์์ ์ถ์ ๊ด์ฐฐ ๋น๊ต์์๋ ์น๋ฃ๊ตฐ๊ณผ ๋์กฐ๊ตฐ ์ฌ์ด์ ์ฑ๋ณ, ๋์ด, ์ฃผ์ฆ์ ๋ฑ์ ์ ์ํ ์ฐจ์ด๋ ์์์ผ๋, ์ฃผ๋น ๋ฐฐ๋ณ ํ์, ๋ฐฐ๋ณ ์๊ฐ, ๋ณ ๋ชจ์์ Bristol๋ถ๋ฅ ๋ฑ์์ ์ ์ํ ์ฐจ์ด๋ฅผ ๋ณด์ฌ, BT๊ฐ PFD์ ์ฆ์์ ํธ์ ์ํจ๋ค๋ ๊ฒ์ ์ ์ ์์๋ค. ํ์ง๋ง ์ถ์ ๊ด์ฐฐ์์ ์น๋ฃ์ ๋ํ ์ฃผ๊ด์ ๋ง์กฑ๋์ ๋ณ์ง๋ฆผ์ ํธ์ ์ ๋ ๊ตฐ ๊ฐ์ ์ ์ํ ์ฐจ์ด๋ฅผ ๋ณด์ด์ง ์์๋ค. ์ง์ฅ ํญ๋ฌธ๊ธฐ๋ฅ๊ฒ์ฌ ๋ฐ BT์ ๋ํ ๊ฑฐ๋ถ๊ฐ์ ์น๋ฃ ์ฑ๊ณต๋ฅ ๊ณผ ์ง์ ์ ๊ด๋ จ์ด ์์๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001047113
|
oai_dc
|
์๋ํ๋๋ก ์ธํด ๋ฐ์ํ ์ค์ฆ ๋จ๋ฐฑ-์๋์ง ์์์ค์กฐํ์์์ ๋๋ฐ๋ ๊ตฌ๋ฆฌ๊ฒฐํ์ฆ ๋นํ 1์
|
Copper Deficient Anemia in Severe Protein-EnergyMalnutrition due to Child Abuse
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋ณ์ฑํ(๋ถ๋น์ฌ์๋ณ์); ์ ์ ๋(๋ถ๋น์ฌ์๋ณ์); ์ฅ์ํฌ(๋ถ๋น์ฌ์๋ณ์)"
] |
์ ์๋ค์ ๊ฐ์กฑ ๋ด์์ ์๋ํ๋๋ก ์ธํด ๋ฐ์ํ ์น๋ช
์ ์ธ ์ค์ฆ ์์์ค์กฐ๋ฅผ ๋ณด์ธ 5์ธ ์ฌ์์ ๋๋ฐ๋ ๋นํ๊ณผ ๊ตฌ๋ฆฌ ๊ฒฐํ์ฆ์ WHO ์น๋ฃ ์ง์นจ๊ณผ ๊ตฌ๋ฆฌ ๋ณด์ถฉ์๋ฒ์ผ๋ก ํธ์ ์ํจ 1์๋ฅผ ์นํํ์๊ธฐ์ ๋ณด๊ณ ํ๋ ๋ฐ์ด๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001047114
|
oai_dc
|
์์๊ธฐ Churg-Strauss Syndrome 1์
|
A Case of Churg-Strauss Syndrome in Infancy
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์์๋ฏผ(๊ณ๋ช
๋ํ๊ต); ๊น๊ต์ผ(๊ณ๋ช
๋ํ๊ต); ๋ฐ๋ฌธํธ(๊ณ๋ช
๋ํ๊ต); ๊ฐ์ ๋(๊ณ๋ช
๋ํ๊ต); ์ดํฌ์ (๊ณ๋ช
๋ํ๊ต); ํฉ์ง๋ณต(๊ณ๋ช
๋ํ๊ต)"
] |
์ ์๋ค์ ๋ง์ด ํ์ก ํธ์ฐ๊ตฌ์ ์ฆ๊ฐ, ๋ฐ๋ณต์ ์ธ ์ฒ์, ๊ณ ์ ๋์ง ์์ ํ ์นจ์ค, ๊ทธ๋ฆฌ๊ณ ์์ฅ๊ด ์ถํ ๋ฐ ํ๊ด ์ธ ํธ์ฐ๊ตฌ ์นจ์ค์ ๋ณด์ธ ์์์์ p-ANCA์ c-ANCA์ ์ฆ๊ฐ ์๊ฒฌ๊ณผ ์คํ
๋ก์ด๋ ์ฌ์ฉ ํ ์ฆ์๊ณผ ๊ฒ์ฌ ์๊ฒฌ์ด ๊ธ๊ฒฉํ ํธ์ ์ ๋ฐ๋ณต์ ์ผ๋ก ๋ณด์ด๋ ์์ ์๊ฒฌ์ ๊ทผ๊ฑฐ๋ก ์ง๋จ๋ ์์๊ธฐ CSS 1์๋ฅผ ๊ฒฝํํ์๊ธฐ์ ๋ณด๊ณ ํ๋ ๋ฐ์ด๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001047115
|
oai_dc
|
์์์์ ๋ฐ์ํ ์์ฅ๊ด ๊ฐ์ง ์ข
์ 1์
|
A Case of Gastrointestinal Stromal Tumor in a Child
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ค๊ฒฝ๋น(์ถฉ๋จ๋ํ๊ต); ๊น์ฌ์(์ถฉ๋จ๋ํ๊ต); ์ ์ฌํ(์ถฉ๋จ๋ํ๊ต); ์ค์ง์(์ถฉ๋จ๋ํ๊ต); ๊ฐ๋์(์ถฉ๋จ๋ํ๊ต)"
] |
์ ์๋ค์ 2๋
์ ๋ถํฐ ์์ฌ ํ์ ์ฃผ๋ก ๋ํ๋๋ ๊ฐํ์ ์ธ ์๋ณต๋ถ ๋ณตํต์ด ์์ด์ค๋ค๊ฐ ํ ์ฐจ๋ก ํํ๋ณ์ ๋ณด์ฌ ์ธ๊ทผ ๋ณ์์์ ์ํํ ํ์ก๊ฒ์ฌ์์ ๋นํ์ ๋ณด์ฌ ์ ์๋ 10์ธ ์ฌ์์์ ์์์์๋ ๋ฐ์์ด ๋๋ฌผ๋ค๊ณ ์๋ ค์ง ์์์ ๋ฐ์ํ GIST 1์๋ฅผ ๊ฒฝํํ์๊ธฐ์ ๋ฌธํ๊ณ ์ฐฐ๊ณผ ํจ๊ป ๋ณด๊ณ ํ๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001047119
|
oai_dc
|
์๊ฐ๋ฉด์ญ๊ฐ์ผ๊ณผ ์๋ฐ์ฑ ๊ฒฝํ๋ด๊ด์ผ์ ๊ฐ์ง์ค๋ณต์ฆํ๊ตฐ ์์ ํ์์์ ๋ฐ์ํํ์ง์ธํฌ์ฑ ๊ณจ์์ผ 1์
|
A Case of Chronic Lymphoplasmacellular Osteomyelitiswith Autoimmune Hepatitis/Primary SclerosingCholangitis Overlap Syndrome in a Child
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ด์งํ(์ฑ๊ท ๊ด๋ํ๊ต); ์ดํ์(์ฑ๊ท ๊ด๋ํ๊ต); ๊น์ง๊ท(์ฑ๊ท ๊ด๋ํ๊ต); ์ด์งํ(ํ๋ฆผ๋ํ๊ต); ์ต์ฐํธ(์ฑ๊ท ๊ด๋ํ๊ต)"
] |
์ ์๋ค์ 4์ธ์ ์ง๋จ๋ ์๊ฐ๋ฉด์ญ๊ฐ์ผ๊ณผ ๊ถค์์ฑ ๋์ฅ์ผ ๊ทธ๋ฆฌ๊ณ 6์ธ์ ์ง๋จ๋ ์๋ฐ์ฑ ๊ฒฝํ๋ด๊ด์ผ์ ๊ฐ์ง ์ค๋ณต์ฆํ๊ตฐ ํ์์์ 9์ธ์ ๋ง์ฑ ๋ฆผํํ์ง์ธํฌ์ฑ ๊ณจ์์ผ์ด ๋ฐ๋ณํ ๋ค ๋ฉด์ญ์ต์ ์น๋ฃ์ ์ ๋ฐ์ํ์ง ์๋ ์ฆ๋ก๋ฅผ ๊ฒฝํํ์๊ธฐ์ ๋ณด๊ณ ํ๋ ๋ฐ์ด๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001047117
|
oai_dc
|
์์์ ๊ฒฐ์ฅ์์ ๋ฐ์ํ ์๋ฐ์ฑ ์ ์์ข
1์
|
A Case of Mucinous Adenocarcinoma of the SigmoidColon in a Child
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ ์ฌ์ด(๋๊ตญ๋ํ๊ต); ์์ ๊ฒฝ(๋๊ตญ๋ํ๊ต); ๊น์ ์(๋๊ตญ๋ํ๊ต); ์ด์ ์ฃผ(๋๊ตญ๋ํ๊ต); ์กฐ์ฑ๋ฏผ(๋๊ตญ๋ํ๊ต); ์ด๋์(๋๊ตญ๋ํ๊ต); ๊น๋๊ถ(๋๊ตญ๋ํ๊ต); ์ต์ฑ๋ฏผ(๋๊ตญ๋ํ๊ต); ๊น๋ํ(๋๊ตญ๋ํ๊ต)"
] |
์์์ ์ฒญ์๋
๊ธฐ์ ๋ฐ์ํ๋ ๋์ฅ์ ์
์ฑ ์ข
์์ ๋งค์ฐ ๋๋ฌผ๊ณ ์ํ๊ฐ ๋ถ๋ํ๋ค. ์ ์๋ค์ ๋ด์ 3๊ฐ์ ์ ๋ถํฐ์ ์์ ๋ถ์ง, ์ฒด์ค ์ฆ๊ฐ ์ง์ฐ๊ณผ ๋ด์ 6์ผ ์ ๋ถํฐ์ ์ค์ฌ, ๋ณตํต, ๋ณต๋ถ ์ข
๊ดด ์ด์ง๋ฅผ ์ฃผ์๋ก ๋ด์ํ 12์ธ ๋จ์์์ ๋ณต๋ถ ์ด์ํ ์ดฌ์, ๋ณต๋ถ ์ ์ฐํ ๋จ์ธต ์ดฌ์, ๋ฐ๋ฅจ ๋์ฅ ์กฐ์์ , ๋์ฅ ๋ด์๊ฒฝ ๊ฒ์ฌ ๋ฐ ์กฐ์ง ๊ฒ์ฌ ์๊ฒฌ์ผ๋ก ์ง๋จ๋ S์ ๊ฒฐ์ฅ์ ๋ฐ์ํ ์ ์ก ์ ์์ข
1์๋ฅผ ๊ฒฝํํ์๊ธฐ์ ๋ฌธํ ๊ณ ์ฐฐ๊ณผ ํจ๊ป ๋ณด๊ณ ํ๋ ๋ฐ์ด๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001241379
|
oai_dc
|
๊ฑฐ๋ ๊ฐ ์ข
๊ดด์ ์ฌ๋ฐฉ ์ค๊ฒฉ ๊ฒฐ์์ ๋๋ฐํ Abernethy ๊ธฐํ 2ํ 1์
|
A Case of Congenital Extra Hepatic Portocaval Shunt (Abernethy Malformation Type 2) with a very Large Liver Mass and an Atrial Septal Defect
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ดํด์ (์ฑ๊ท ๊ด๋ํ๊ต); ์ด์งํ(ํ๋ฆผ๋ํ๊ต); ํ์ค(์ฑ๊ท ๊ด๋ํ๊ต); ๊ฐ์ด์(์ฑ๊ท ๊ด๋ํ๊ต); ์ดํฅ์ฌ(์ฑ๊ท ๊ด๋ํ๊ต); ์์ฐ๋ฆผ(์ฑ๊ท ๊ด๋ํ๊ต); ์ ์์(์ฑ๊ท ๊ด๋ํ๊ต); ์ต์ฐํธ(์ฑ๊ท ๊ด๋ํ๊ต)"
] |
Extrahepatic portosystemic shunts, known as Abernethy malformations, were first reported by John Abernethy in 1793. They are classified into two types: Type I refers to a congenital absence of the portal vein and Type II refers to a shunt involving a side-to-side anastomosis with reduced portal blood flow into the liver parenchyma. This malformation is so rare that less than 100 cases have been reported in the medical literature. We report the case of a 13-month-old boy who had a congenital extrahepatic portocaval shunt with a hypoplastic portal vein. This case was complicated with an atrial septal defect and a large hyperplastic nodule in the liver. The patient was diagnosed with a Type II Abernethy malformation. We planned on surgical occlusion of the extrahepatic portocaval shunt. However, six months later, the patient had a sudden onset of a fever of unknown origin and developed hepatic encephalopathy. Although he underwent a liver transplantation, he died of acute hepatic failure.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001241391
|
oai_dc
|
๊ฐ๊ด ํ์์ฆ์ด ๋๋ฐ๋ ์๋ผ์ง ์ฆํ๊ตฐ (Alagille Syndrome) 1์
|
A Case of Alagille Syndrome with Atresia of the Hepatic Duct
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊นํจ์ (์ฐ์ธ๋ํ๊ต); ๊ณ ํ(์ฐ์ธ๋ํ๊ต); ์ ๊ธฐ์ญ(์ฐ์ธ๋ํ๊ต); ์ค์ ํ(์ฐ์ธ๋ํ๊ต); ๋ฐ์๋
(์ฐ์ธ๋ํ๊ต); ๊น๋ช
์ค(์ฐ์ธ๋ํ๊ต)"
] |
A two-month-old baby had acholic stool, neonatal hyperbilirubinemia and congenital heart disease. Atresia of the hepatic duct was confirmed by open cholangiography, which showed a non-opacified intrahepatic bile duct. Liver biopsy and the Kasai operation were performed. Because the liver biopsy pathology revealed a paucity of intrahepatic bile ducts, the patient was diagnosed with the Alagille syndrome. We report the case of an infant diagnosed with the Alagille syndrome with atresia of the hepatic duct.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001241392
|
oai_dc
|
์ ์ ๋ฉด์ญ๊ธฐ๋ฅ์ ๊ฐ์ง ์์์์ ์๋ ๊ฐ์ผ ํ์ ๋ฐ์ํ ๊ธ์ฑ ์ท์ฅ์ผ 1์
|
Acute Pancreatitis Associated with Varicella Infection in an Immunocompetent Child
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ค๊ธฐ์(์ธ์ฐ๋ํ๊ต); ๊น์ค์ฑ(์ธ์ฐ๋ํ๊ต); ๊น์ํ(์ธ์ฐ๋ํ๊ต); ๋ฐ์๊ท(์ธ์ฐ๋ํ๊ต); ์ ์ง์(์ธ์ฐ๋ํ๊ต)"
] |
Blunt trauma, drugs, infection, congenital anomalies of the pancreaticobiliary system, and multisystem diseases are the main causes of acute pancreatitis in children. Various viruses can cause acute pancreatitis, but varicella-induced pancreatitis is unusual and generally observed in adults or immunocompromised patients. We report a rare case of acute pancreatitis associated with varicella-zoster virus infection in a 6-year-old immunocompetent girl. The patient initially presented complaining of severe abdominal pain and repetitive vomiting. The patient had multiple cutaneous crusts that has been caused by preceding varicella infection and had elevated values of serum amylase and lipase. Abdominal ultrasonography demonstrated swelling of the pancreas and pancreatic duct dilatation, findings which were compatible with acute pancreatitis. The patient's clinical and laboratory abnormalities were completely normalized through conservative treatment consisting of fasting, total parenteral nutrition, and analgesic therapy.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001241394
|
oai_dc
|
์์๋ ์ญ๋ฅ์ ํ ํก์ธ ์ง๋จ ๋ฐฉ๋ฒ์ผ๋ก์ ์์๋ ์ญ๋ฅ ์ ํฐ๊ทธ๋ํผ์ ์ ์ฉ์ฑ
|
The Usefulness of Scintigraphy for the Detection of Gastroesophageal Reflux and Pulmonary Aspiration
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊ฐ์ฑ๊ธธ(์ธํ๋ํ๊ต); ํ์ธ์(์ธํ๋ํ๊ต); ์๋ํ(์ธํ๋ํ๊ต); ๊น์ ํฌ(์ธํ๋ํ๊ต); ์๋ณ๊ด(์ธํ๋ํ๊ต)"
] |
Purpose: Chronic pulmonary disease may be caused by aspiration of gastric contents secondary to gastroesophageal reflux. At present, there is no gold standard for documenting pulmonary aspiration. The purpose of this study was to investigate the usefulness of radionuclide scintigraphy in the detection of gastroesophageal reflux and pulmonary aspiration.
Methods: Thirty-five patients with suspected aspiration pneumonia, and five normal control subjects, were included in the study. All subjects underwent gastroesophageal reflux scintigraphy after the ingestion of a 99mTc-tin colloid mixture. Dynamic images to detect gastroesophageal reflux were obtained for 1 hour. Additional static images of the chest, to detect lung aspiration, were obtained at 6 and 24 hours after oral ingestion of the tin colloid. In addition to visual analysis, pulmonary aspiration was quantitated by counting the number of pixels labeled with radioactive isotope in the region of interest (ROI) of both lung fields. Aspiration index (AI) was obtained by subtracting the pixel counts of the background from the pixel counts of the ROI.
Results: Among 35 patients with suspected aspiration pneumonia, 23 proved to have gastroesophageal reflux by scintigraphy. One patient showed definite pulmonary accumulation of activity by visual analysis of the 6-hour image. Thirty of 35 (85.7%) patients showed higher AI beyond the upper limit of AI in the healthy controls. When we compared the reflux group with the non-reflux group, there was a significantly higher AI at 6 hours in the reflux group (p๏ผ0.05).
Conclusion: The results suggest that radionuclide scintigraphy is useful in detecting small pulmonary aspiration in patients with suspected aspiration pneumonia secondary to reflux.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001241396
|
oai_dc
|
Infliximab: ๋ถ์์ฑ ํฌ๋ก ๋ณ ์น๋ฃ๋ฒ์ผ๋ก์์ ์ ์ฉ์ฑ๊ณผ Top-down ๊ดํด ์ ๋ ์๋ฒ์ผ๋ก์์ ๊ฐ๋ฅ์ฑ
|
Infliximab: The Benefit for Refractory Crohn Disease and Top-down Induction Therapy in Severe Crohn Disease
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ด์งํ(ํ๋ฆผ๋ํ๊ต); ๋ฐ์ฑ์(์ฑ๊ท ๊ด๋ํ๊ต); ์ต์ฐํธ(์ฑ๊ท ๊ด๋ํ๊ต); ์ดํด์ (์ฑ๊ท ๊ด๋ํ๊ต)"
] |
Purpose: The aim of this study is to report the efficacy of infliximab, a monoclonal antibody directed against tumor necrosis factor alpha which is used for both treatment of refractory pediatric Crohn disease (CD) and induction of remission.
Methods: Among pediatric patients who were diagnosed with CD at Samsung Medical Center between March 2001 and August 2007, a total of 16 patients were given infliximab to treat conventional therapy- resistant refractory CD and severe active CD for induction of remission. Patients needing maintenance therapy were treated with an infliximab infusion every 8 weeks, and fistulizing CD patients occasionally received the infusion upon the condition that a fistula developed. The efficacy of treatment was assessed by comparing the Pediatric Crohn Disease Activity Index (PCDAI), Hct, ESR, CRP, and serum albumin levels using paired t-test.
Results: The male/female ratio was 13๏ผ3, and the median age was 13 years (range, 21 monthsโผ15 years). The patients included 7 cases of therapy-resistant refractory CD, 7 cases of severe active CD, and 2 cases of fistulizing CD. Mean PCDAI before infliximab therapy was 34.19ยฑ14.96, and mean follow-up PCDAI within 2 to 4 weeks after the last infusion was significantly lower, at 6.88ยฑ10.31 (p= 0.000). Hematological markers such as ESR (p=0.000), serum albumin (p=0.016), and CRP (p=0.009) also improved significantly after infusion. Remission was achieved in 2 of 4 patients refractory to conventional therapy. Among 3 steroid-dependent patients, 2 were able to discontinue steroid therapy, and dose reduction was possible in 1 patient. Remission after top-down therapy without prior use of other immunomodulators was achieved in 6 weeks in all 7 of the patients who had severe CD. Nine of ten refractory fistulizing CD patients also showed improvement after infliximab therapy.
Conclusion: Infliximab was effective in pediatric refractory CD for induction of remission and maintenance therapy, as well as in severe CD for top-down induction therapy. Furthermore, infliximab has contributed to steroid cessation and dose reduction. Long-term follow-up evaluation is needed to determine safety and efficacy of infliximab in the future.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001241390
|
oai_dc
|
์ ์ฒ์ฑ ๊ฐ ์ฌ์ ์ฆ์ ๋๋ฐํ Kabuki ์ฆํ๊ตฐ 1์
|
A Case of Congenital Hepatic Fibrosis in Kabuki Syndrome
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋ฐ์ฌํ(๊ณ๋ช
๋ํ๊ต); ์ ๋ช
ํ(๊ณ๋ช
๋ํ๊ต); ์ดํฌ์ (๊ณ๋ช
๋ํ๊ต); ์ด์งํ(ํ๋ฆผ๋ํ๊ต); ์ต์ฐํธ(์ฑ๊ท ๊ด๋ํ๊ต); ์ก์์ฉ(์ฑ๊ท ๊ด๋ํ๊ต); ์์ฐ๋ฆผ(์ฑ๊ท ๊ด๋ํ๊ต); ํฉ์ง๋ณต(๊ณ๋ช
๋ํ๊ต)"
] |
Kabuki syndrome is characterized by peculiar facial features, developmental delay, and mental retardation. Congenital hepatic abnormalities in Kabuki syndrome patients have been sporadically reported in the literature and consist of extrahepatic biliary atresia, neonatal sclerosing cholangitis, and transient neonatal cholestasis. We report here a case of congenital hepatic fibrosis in a patient with Kabuki syndrome. To our knowledge, only one case of congenital hepatic fibrosis has been reported in the setting of Kabuki syndrome.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001241398
|
oai_dc
|
์์ ์ ๊ฑด๊ฐ๊ฒ์ง ์์ ๋ฌธ์ง ๋ฐ ์ง์นจ ๊ฐ๋ฐ
|
Development of a Nutrition Questionnaire and Guidelines for the Korea National Health Screening Program for Infants and Children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋ฌธ์ง์(์ธ์ ๋ํ๊ต); ๊น์ฌ์(์ถฉ๋จ๋ํ๊ต); ์ฅ์ํฌ(๋ถ๋น์ ์๋ณ์); ์ต๊ดํด(์๋จ๋ํ๊ต); ์ํ๋(์์ธ๋ํ๊ต); ์์ ๊ธฐ(์์ธ๋ํ๊ต); ๊ณ ์ฌ์ฑ(์์ธ๋ํ๊ต); ์ต๊ฒฝ๋จ(์์๋ณ์); ์์ ์(์ดํ์ฌ์๋ํ๊ต); ์ ํฌ์ (๊ตญ๋ฏผ๊ฑด๊ฐ๋ณดํ๊ณต๋จ); ์๋ฐฑ๋ฆฐ(๊ณ ๋ ค๋ํ๊ต); ํฉ์น์(์ง๋ณ๊ด๋ฆฌ๋ณธ๋ถ); ์์๋ ค(์ง๋ณ๊ด๋ฆฌ๋ณธ๋ถ); ๊นํ์(๋ณด๊ฑด๋ณต์ง๋ถ)"
] |
Purpose: A new health policy, referred to as the National Health Screening Program for Infants and Children, was launched in November 2007 by the Ministry of Health and Welfare and National Health Insurance Corporation in Korea. We have developed a nutrition-counseling program that was incorporated into this project.
Methods: We reviewed the nutritional guidelines published by The Korean Pediatric Society and internationally well-known screening programs such as Bright Future in the United States. We also reviewed the recent Korean national surveys on nutritional issues, including the Korea National Health and Nutrition Examination Survey (KNHANES) and the 2005 National Survey of Physical Body and Blood Pressure in Children and Adolescents. The development of questions, pamphlets, computer programs, and manuals for doctors was carried out after several meetings of researchers and governmental officers.
Results: We summarized the key nutritional issues according to age, including breastfeeding in infants, healthier complementary feeding, and prevention of iron deficiency anemia, establishment of healthier diets, as well as dietary prevention of overweight children with an emphasis on physical exercise. We have constructed a new Korean nutrition questionnaire and an anticipatory guidance program based on the primary care schedule of visits at 4, 9, 18, 30, and 60 months of age. Five to eight questions were asked at each visit and age-matched pamphlets for parents and guidelines for doctors were provided.
Conclusion: We developed a nutrition-counseling program based on recent scientific evidence for Korean infants and children. Further research on this national program for screening the nutritional problems in detail and setting the therapeutic approaches may help identify areas of success as well as those that need further attention.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001241399
|
oai_dc
|
์์ ๋ฒ ์ฒดํธ ๋ณ์์ ๋ฐ์๋ ๋ณต๋ถ ์ฒ๊ณต 1์
|
Multiple Intestinal Perforations in a Child with Behcet's Disease
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ต๊ธ์ฅ(์ฐ์ธ๋ํ๊ต); ๊ณ ํ(์ฐ์ธ๋ํ๊ต); ์ ๊ธฐ์ญ(์ฐ์ธ๋ํ๊ต)"
] |
Behcet's disease (BD) is a multisystem inflammatory disorder dominated clinically by recurrent oral and genital ulceration, uveitis and erythema nodosum. BD is very rare in children, especially those less than 10 years of age, who account for only an estimated 5% of all cases. Gastrointestinal ulcers, in patients with Behcet's disease with intestinal involvement are rare and have been reported in only 1-2% of all cases. The intestinal ulcers of Behcet's disease are usually multiple and scattered and tend to cause perforations associated with significant morbidity. Patients with BD and abdominal symptoms must be evaluated thoroughly for potential perforation of the gastrointestinal tract. Here we report the case of a 4 year 9 month old child with multiple perforations of the gastrointestinal tract associated with BD.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001241397
|
oai_dc
|
์ํ ๋จ๋ฐฑ์ง ์ ๋ฐ์ฑ ์ง๊ฒฐ์ฅ์ผ์์ ์ํ ํน์ด IgE ํญ์ฒด ๊ฒ์ฌ์ ์์์ ์์
|
Clinical Significance of Food-specific IgE Antibody Tests in Food Protein-induced Proctocolitis
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ก์ ์ค(๊ณ๋ช
๋ํ๊ต); ๊ฐ์ ๋(๊ณ๋ช
๋ํ๊ต); ๊น์ฌ๋ฃก(๊ณ๋ช
๋ํ๊ต); ํฉ์ง๋ณต(๊ณ๋ช
๋ํ๊ต)"
] |
Purpose: The aim of this study was to determine the clinical significance of food-specific IgE antibody tests in detecting triggering antigens in food protein-induced proctocolitis (FPIPC).
Methods: Between February 2006 and May 2007, data from 16 consecutive FPIPC patients that underwent MAST and Uni-CAP tests on initial visits, were reviewed. The endoscopic criterion used for establishing a diagnosis of FPIPC was an increase in the number of eosinophils in the lamina propria (โฅ60 per 10 high power fields). Offending foods were suspected clinically based on elimination and challenge testing to mother or patient diets with the following five highly allergenic foods: dairy products, eggs, nuts and soybean, fish and shellfish, and wheat and buckwheat. We compared the results of initial MAST or Uni-CAP tests with clinically suspected offending foods.
Results: For the 16 FPIPC patients, MAST tests showed positive results in 2 patients (12.5%), and Uni-CAP tests showed positive results in 3 patients (18.8%). Through clinical elimination and challenge, the 33 offending foods were identified: 7 fish and shellfish (21.2%), 6 eggs (18.2%), 6 wheat and buckwheat (18.2%), 4 dairy products (12.1%), 3 soybean (9.1%), 3 pork (9.1%), 2 nuts (6.1%), 1 beef (3.0%), and 1 mushroom (3.0%). Clinically suspected offending foods and MAST and Uni-CAP test results were found to be correlated in 1 patient (6.7%) each.
Conclusion: Food specific IgE antibody tests are inappropriate for predicting offending foods in FPIPC. Clinical food elimination and challenge testing provide useful means of detecting offending foods.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001241681
|
oai_dc
|
์์ ์ด๋ฌผ์ ์ํ ์-์ญ์ด์ง์ฅ ๋๊ณต 1์
|
A Case of Gastroduodenal Fistula Caused by Ingested Magnetic Foreign Bodies
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ด์ํฌ(์กฐ์ ๋ํ๊ต); ๋ฏผ์๋(์กฐ์ ๋ํ๊ต); ๋ฌธ๊ฒฝ๋(์กฐ์ ๋ํ๊ต)"
] |
If multiple magnets are ingested, the potential exists for the magnets attracting one another across the gastrointestinal tract and inducing pressure necrosis, perforation, fistula formation, or intestinal obstruction. We report the case of a 12-year-old boy who suffered from a fistulous communication between the lesser curvature of the mid-body of the stomach and the duodenal bulb, caused by 4 ingested magnets (Singing Magnets, China). The patient presented with moderate mental retardation, a one-year history of cyclic vomiting, and abdominal discomfort. We present the findings of simple abdominal radiography, esophagogastroduodenoscopy, computed tomography, and upper gastrointestinal series. An emergency exploratory laparotomy was performed, which revealed a gastroduodenal fistula. Fistula repair and the removal of 4 magnetic toys were subsequently performed. We emphasize that clinicians who care for children should be aware of the hazards of magnetic toy ingestion.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001241393
|
oai_dc
|
๋ง์ฑ Bํ ๊ฐ์ผ ์๋ด: ๊ตญ๋ด ์ธํฐ๋ท ์์ ํํ ์ค๋ฅ๋ฅผ ์ค์ฌ์ผ๋ก
|
Consulting about Chronic Hepatitis B: Focusing on Common Errors of Internet Website in Korea
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ต๋ณํธ(๊ฒฝ๋ถ๋ํ๊ต)"
] |
Comprehensive understanding of the natural course of chronic hepatitis B virus (HBV) infection is mandatory for the management and treatment of chronic hepatitis B, of which the natural course consists of immune tolerance, immune clearance, inactive carrier state, and reactivation phase. Evidence based medical approach is essential for the management of HBV carriers and treatment of active hepatitis to decrease risks of liver cirrhosis and hepatocellular carcinoma as well as to increase survival. In addition, education of patients or their parents are required to achieve a better therapeutic outcome and to prevent unconfirmed alternative medicine and anecdotal approaches.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001241395
|
oai_dc
|
์์์ฒญ์๋
์ง์ ๋ด์๊ฒฝ: ๋ํ์์์ํ๊ธฐ์์ํํ ํ์ ์์ํ ์กฐ์ฌ ๋ณด๊ณ
|
Pediatric Endoscopic Sedation in Korea: A Survey of the Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋ฅ์ผ(๊ฐ์ฒ์๊ณผํ๋ํ๊ต); ๊น๊ฒฝ๋ชจ(์ธ์ฐ๋ํ๊ต); ๋ํ์์์ํ๊ธฐ์์ํํ ํ์ ์์ํ(๋ํ์์์ํ๊ธฐ์์ํํ ํ์ ์์ํ)"
] |
Purpose: The aim of this survey was to analyze the choice of sedative drugs and their side effects during pediatric endoscopic sedation in Korea. We also evaluated doctors, caretakers and patient satisfaction with the procedures.
Methods: Between June 2006 and July 2006, a 16-item survey regarding current sedation practices, during one month, was mailed to 28 hospitals in Korea. The results of the survey responses were then analyzed. Results: Endoscopy performed under conscious sedation was reported in 89.0% of the responders and endoscopy under general anesthesia in 0.9% of 465 endoscopic procedures. Endoscopy under conscious sedation was performed in 89.1% for upper gastrointestinal endoscopy (GFS) and 88.1% for lower GFS. Midazolam was used for conscious sedation during the endoscopy in 84.5% of cases and propofol was used in two cases (0.5%). In addition, a bezodiazepine/opioid combination was used iin 84.6% (44 cases) for lower GFS. Patients were monitored with pulse oxymetry, EKG (91.4%) as well as automatic BP (5.1%). Transient hypoxia was the only side effect noted and was treated with supplemental oxygen (4.6%). Flumazenil was used in 2.71% of cases. The choice of sedation was made by the endoscopist (84%). The satisfaction rate for endoscopists was 68%, and for the patients and caretakers was 84% (as reported by the endoscopists).
Conclusion: Midazolam was used only for the upper GFS and benzodiazepine/opioid combination was used for the lower GFS in Korea. The rate of satisfaction was relatively high and there were no significant side effects noted during the endoscopy under conscious sedation.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001240602
|
oai_dc
|
๊ฑด๊ฐํ๋ ๋จ์์์ ๋ฐ์๋ ํค๋ฅดํ์ค ์๋์ผ 1์
|
A Case of Herpes simplex Esophagitis in an Immunocompetent Boy
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ฌ์ค์(๋ถ๋น์ ์๋ณ์); ์ ์ ๋(๋ถ๋น์ ์๋ณ์); ์ฅ์ํฌ(๋ถ๋น์ ์๋ณ์)"
] |
Herpes simplex virus has rarely been identified as a cause of esophagitis in immunocompetent children. This virus affects predominantly males presenting with symptoms of fever, odynophagia, dysphagia, and retrosternal pain of acute onset. Esophagoscopy typically reveals exudative well-circumscribed ulcerations of the distal and/or mid-esophagus. Further investigations using biopsy, viral culture, polymerase chain reaction (PCR), and seroconversion of antibodies to Herpes simplex are recommended to assist with a definitive diagnosis. This esophagitis is often a self-limited infection in immunocompetent children. Nevertheless, antiviral treatment may expedite symptom relief with Herpes simplex virus infection. It is imperative to document herpes esophagitis in cases with subsequent severe odynophagia in immunocompetent children. Here we present the case of a 12-year-old immunocompetent boy with herpes esophagitis
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001081659
|
oai_dc
|
์ํ ๋จ๋ฐฑ์ง ์ ๋ฐ์ฑ ์ฅ์ผ ์ฆํ๊ตฐ:์์์ ์ ๊ทผ๊ณผ ๋ณํ์๋ฆฌ์ ์ต์ ์ง๊ฒฌ
|
Current Status of Pediatric Liver Transplantation
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"ํฉ์ง๋ณต(๊ณ๋ช
๋ํ๊ต)"
] |
Food protein-induced enterocolitis syndrome (FPIES) is a non-IgE mediated hypersensitivity disorder, which is associated with mainly gastrointestinal symptoms and has a delayed onset. The vomiting and/or diarrheal symptoms of FPIES typically begin in the first month of life in association with a failure to thrive, metabolic acidosis, and shock. Therefore, the differential diagnosis of FPIES and neonatal or infantile sepsis-like illnesses or gastroenteritis is difficult. The early recognition of indexes of suspicion for FPIES may help in the diagnosis and treatment of this disorder. The diagnosis of FPIES is generally made through clinical practice and food-specific IgE test findings are typically negative in this condition. Therefore, oral cow's milk challenge (OCC) remains the valid diagnostic standard for FPIES. An investigation of positive OCC outcomes helps to find out a diagnostic algorithm of criteria of a positive challenge in FPIES. Moreover, it has not been clearly determined in infantile FPIES when 1st follow up-oral food challenge (FU-OFC) should be performed, with what kind of food protein (e.g., cow's milk, soy), and how much protein should be administered. Hence, to prevent the risk of inappropriate FU-OFC or accidental exposure and achieve appropriate dietary management, it is necessary to identify tolerance rates to major foods under the careful follow up of infantile FPIES patients. On the other hand, small intestinal enteropathy with villous atrophy is observed in FPIES and this enteropathy seems to be in part induced by both of epithelial apoptosis and intercellular junctional complex breakdown. The purpose of this report is to introduce an update on diagnostic and therapeutic approaches in FPIES and suggest the possible histopathological evidences in this disorder. (Korean J Pediatr Gastroenterol Nutr 2007; 10: 117โผ128)
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001081660
|
oai_dc
|
ํ๋๊ธฐ ์์์์ ๋ฐ๋ณต์ฑ ์ฌ๋ฐ์ฑ ๋ณตํต๊ณผ ๋ถ์ ์ฑํฅ๊ณผ์ ๊ด๋ จ์ฑ
|
The Relationship of between Anxiety Tendency and Recurrent Abdominal Pain in Elementary School Children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋ฌธ์ง์(์กฐ์ ๋ํ๊ต); ๋ฌธ๊ฒฝ๋(์กฐ์ ๋ํ๊ต)"
] |
๋ชฉ ์ : ๋ณตํต์ ์์์์ ํํ ๋ณด๋ ์ํ๊ธฐ ์ฆ์ ์ค์ ํ๋์ด๋ค. ๋ณตํต์ด ์ง์์ ์ผ๋ก ๋ฐ๋ณต๋๋ฉด ๋ถ์์ด๋ ์ฐ์ธ์ฆ ๊ฐ์ ์ ์์ ์ฅ์ ๋ฅผ ํธ์ํ๊ฒ ๋๋ค. ๊ทธ๋ฆฌ๊ณ ์ด๋ก ์ธํด ์ด๋ฆฐ์ด๋ค์ ์ ์์ ๋ฐ๋ฌ ๋ฐ ์ธ๊ฒฉํ์ฑ์ ๋ถ์ ์ ์ธ ์ํฅ์ ๋ฏธ์น๊ณ , ๋ค๋ฅธ ์ฌ๋ฌ ๊ฐ์ง ์ ์ ์ ์ ์ฒด์ ์ ์์ ์ ๋ฐ์ํค๊ธฐ๋ ํ๋ค. ์ด์ ์ ์๋ค์ ๋ณตํต๊ณผ ๋ถ์ ์ฑํฅ์ ์ฐ๊ด์ฑ์ ์์๋ณด๊ณ ์์ ๋ณตํต์ ์น๋ฃ์ ์ฌ๋ฆฌ์ ์ธ ์์ธ์ ๊ณ ๋ ค์ ํ์์ฑ์ ํ์ธํ๊ธฐ ์ํ์ฌ ์ฐ๊ตฌ๋ฅผ ์ํํ์๋ค.๋ฐฉ ๋ฒ: ๊ด์ฃผ ๊ด์ฃผ๊ด์ญ์์ ์์ฌํ๋ 1๊ฐ ์ด๋ฑํ๊ต 1ํ๋
๋ถํฐ 6ํ๋
ํ์ 1254๋ช
, ๋จ์ 592๋ช
, ์ฌ์ 662๋ช
์ ๋์์ผ๋ก ๋ณตํต์ ์์์ ํ๊ฐํ์์ผ๋ฉฐ, ๋ถ์์ ์ ๋๋ ํ๊ตญํ ์ํ-ํน์ฑ ๋ถ์๊ฒ์ฌ YZํ(STAI-YZ: Spielberger's State-Trait Anxiety Inventory YZ form) ์ค๋ฌธ์ง๋ฅผ ์ด์ฉํ์ฌ ๋น๊ตใ๋ถ์ํ์๋ค.๊ฒฐ ๊ณผ: 1) ์ ์ฒด 1,254๋ช
์ค ์ง๋ 1๋
๊ฐ ๋ณตํต์ด ์์๋ ์์ด์ ์๋ 709๋ช
(56.5%)์ด์์ผ๋ฉฐ, ์ด ์ค 69๋ช
(5.5%)์ด ๋ง์ฑ ๋ฐ๋ณต์ฑ ๋ณตํต์ด์๋ค. 2) ํน์ฑ ๋ถ์ ๋ฐ ์ํ ๋ถ์์ผ๋ก ์ง๋จํ ์์ด๋ ๊ฐ๊ฐ 116๋ช
(9.3%), 63๋ช
(5.0%)์ด์๋ค. 3) ์ต๊ทผ 1๋
๋์ ๋ณตํต์ด ์์๋ ๊ตฐ๊ณผ ๋ง์ฑ ๋ฐ๋ณต์ฑ ๋ณตํต์ด ์์๋ ๊ตฐ์์ ์์๋ ๊ตฐ์ ๋นํด ํน์ฑ ๋ฐ ํ ๋ถ์ ์ฒ๋๊ฐ ๋ชจ๋ ์์ ์๊ฒ ๋์๋ค. 4) ๋ณตํต์ ์ ๋๊ฐ ์ฌํ ์๋ก ํน์ฑ ๋ฐ ์ํ ๋ถ์ ์ฒ๋๊ฐ ์์ ์๊ฒ ๋์๋ค. 5) ์ํ ๋ถ์ ์ฒ๋๊ฐ ๋์ ์์ด๋ ์ํ ๋ถ์ ์ฒ๋๋ ๋์๋ค. 6) ๋ณตํต์ ๊ธฐ๊ฐ, ๋น๋, ์ง์์๊ฐ, ๋ฐ์์๊ธฐ, ๋ณตํต์ ๋ถ์๋ฅผ ๊ตฌ๋ถํ์์ ๋ ํน์ฑ ๋ฐ ์ํ ๋ถ์ ์ฒ๋์ ์ ์ํ ์ฐจ์ด๊ฐ ์์๋ค. 7) ํน์ฑ ๋ถ์์ด ์๋ ๊ตฐ์ด ๋ณตํต์ ๊ฒฝํํ ํ์์ ๋น์จ์ ์ ์ฒด 116๋ช
์ค 80๋ช
(69.0%)๋ก ํน์ฑ ๋ถ์์ด ์๋ ๊ตฐ 1,138๋ช
์ค 593๋ช
(52.1%)์ ๋นํด ์์ ์๊ฒ ๋ง์๋ค. ์ํ ๋ถ์๊ตฐ์์๋ 63๋ช
์ค 46๋ช
(73%)์ผ๋ก ์ํ๋ถ์์ด ์๋ ๊ตฐ 1,191๋ช
์ค 645๋ช
(59.2%)์ ๋นํด ์์ ์๊ฒ ๋ง์๋ค. 8) ํน์ฑ ๋ถ์์ด ์๋ ๊ตฐ์ RAP์ ๋ํ ์ํ๋๋ ํน์ฑ ๋ถ์์ด ์๋ ๊ตฐ์ ๋นํด 1.96๋ฐฐ ๋์๊ณ , ์ํ ๋ถ์์ด ์๋ ๊ตฐ์ ์๋ ๊ตฐ์ ๋นํด 2.37๋ฐฐ ๋์๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001081846
|
oai_dc
|
์์์์ ์์ฅ๊ด ์ด๋ฌผ์ ์์ฐ ๋ฐฐ์ถ์ ๋ํ ๊ฒฝํ์ ๊ณ ์ฐฐ
|
Spontaneous Passage of Gastrointestinal Foreign Bodies in Children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ด์งํ(์ฑ๊ท ๊ด๋ํ๊ต); ๋จ์ํ(์ฑ๊ท ๊ด๋ํ๊ต); ์ด์งํ(ํ๋ฆผ๋ํ๊ต); ์ดํด์ (์ฑ๊ท ๊ด๋ํ๊ต); ์ต์ฐํธ(์ฑ๊ท ๊ด๋ํ๊ต)"
] |
๋ชฉ ์ : ์์ฅ๊ด ์ด๋ฌผ์ ๋ด์๊ฒฝ์ ์ด๋ฌผ ์ ๊ฑฐ์ ์ด๋ ์์ ์ ์ ๊ฑฐ์ , ๋๋ ์์ฐ ๋ฐฐ์ถ์ ๊ธฐ๋ค๋ฆฌ๋ ๋ฐฉ๋ฒ์ด ์์ผ๋ฉฐ ์ด๋ฌผ์ ์ข
๋ฅ์ ๋ชจ์, ํฌ๊ธฐ, ์ด๊ธฐ ์์น์ ๋ฐ๋ผ ์น๋ฃ ๋ฐฉ๋ฒ์ด ๋ฌ๋ผ์ง ์ ์๋ค. ์์ฐ ๋ฐฐ์ถ์ด ์์๋๋ ์ด๋ฌผ์ ๋ํด์๋ ๋ด์๊ฒฝ์ ์ํํ์ง ์์ ์ ์๋ค. ์ด์ ๋ณธ ์ฐ๊ตฌ์์๋ ์์ฅ๊ด ์ด๋ฌผ์ ์์ฐ ๋ฐฐ์ถ ๊ฒฝ์ฐ์ ๋ด์๊ฒฝ์ ์ ๊ฑฐ ๊ฒฝ์ฐ๋ฅผ ๋น๊ตํ๊ณ , ์์ฐ ๋ฐฐ์ถ ์ด๋ฌผ์ ๊ฒฝ์ฐ์ ์ด๋ฌผ์ ์ข
๋ฅ, ํฌ๊ธฐ, ์ด๊ธฐ ์์น์ ๋ฐ๋ฅธ ์์ฐ ๋ฐฐ์ถ๋ฅ ์ ๋ํด์ ์์๋ณด์๋ค.
๋ฐฉ ๋ฒ: 2001๋
1์๋ถํฐ 2007๋
7์๊น์ง 6๋
๊ฐ ์์ฅ๊ด ๋ด ์ด๋ฌผ์ ์ฃผ์๋ก ์ผ์ฑ์์ธ๋ณ์ ์๊ธ์ค์ ๋ฐฉ๋ฌธํ 160๋ช
์ ๋์์ผ๋ก ํํฅ์ ์๋ฌด๊ธฐ๋ก ์กฐ์ฌ ๋ฐ ๋ณดํธ์ ์ ํ ๋ฉด๋ด์ ํตํด ์ ๋ณด๋ฅผ ์์งํด์ ๊ฐ๊ฐ์ ์ด๋ฌผ๊ฐ์ ํน์ฑ, ์์น, ์์ฐ ๋ฐฐ์ถ์ ์๊ฐ๊ณผ ๋น๋ ๋ฑ์ ์กฐ์ฌํ์๋ค.
๊ฒฐ ๊ณผ: ๋จ๋
๋น๋ 1.46๏ผ1๋ก ๋จ์๊ฐ 95๋ช
(59.4%), ์ฌ์๊ฐ 65๋ช
(40.6%)์ด์๋ค. ์ ์ฒด ์ด๋ฌผ์ ์์ฐ ๋ฐฐ์ถ๋ฅ ์ 48.0%์๋ค. ๊ฐ ์ด๋ฌผ์ ์ข
๋ฅ์ ๋ฐ๋ฅธ ์์ฐ ๋ฐฐ์ถ๋ฅ ์ ๊ฐ๊ฐ ๋์ 36.5%, ํ, ๋จธ๋ฆฌํ, ๋์ฌ, ์ด์ ๋ฑ ๊ธธ๊ณ ๋ ์นด๋ก์ด ์ด๋ฌผ 52.6%, ๋ฐ๋๋๊ณผ ๊ตฌ์ฌ 83.3%, ์์ 69.2%, ๋์คํฌ ๋ฐฐํฐ๋ฆฌ 50.0%์๋ค. ์ด์ค์์ ๋์ ์ ํฌ๊ธฐ์ ์์น์ ๋ฐ๋ผ ๋ด์๊ฒฝ์ ์ ๊ฑฐ ๋น์จ์์ ๋ง์ ์ฐจ์ด๋ฅผ ๋ณด์ฌ 100์ ๋์ ์ ์ด๊ธฐ ์๋์ ๊ฑธ๋ ค์์ ํ๋ฅ ์ด 66.7% (22/33)์๊ณ ์ด ์ค์์ ๋ด์๊ฒฝ์ผ๋ก ์ ๊ฑฐํ ๋น์จ์ 90.9%์๋ค. ํฌ๊ธฐ๊ฐ ๋น์ทํ 100์ ๋์ , 10์ ๋์ ๊ทธ๋ฆฌ๊ณ ๋ฐ๋๋์ ๋์์ผ๋ก ์กฐ์ฌํ ๋์ด๋ณ, ์์น๋ณ ์์ฐ ๋ฐฐ์ถ๋ฅ ์ ์ด๊ธฐ ์ด๋ฌผ์ด ์ ์ดํ์ ์์นํ์ ๊ฒฝ์ฐ ์ ์ฐ๋ น์์ 80% ์ด์์ผ๋ก ๋๊ฒ ์กฐ์ฌ๋์๋ค.
๊ฒฐ ๋ก : ์์์ ์์ฅ๊ด ์ด๋ฌผ์ ์ด๋ฌผ์ ์ข
๋ฅ๋ ํฌ๊ธฐ, ์์น ๋ฑ์ ์์ฐ ๋ฐฐ์ถ๋ฅ ์ด ๋งค์ฐ ๋ค์ํ๋ค. ๋ฐ๋ผ์ ์ ์์ฆ์ด ๋ ๋๋ ๋ด์๊ฒฝ์ ์ด์ฉํ ์ด๋ฌผ ์ ๊ฑฐ๋ฅผ ์ํํ๊ณ , ์์ฐ ๋ฐฐ์ถ๋ฅ ์ด ๋์ ์ด๋ฌผ์ ๊ฒฝ๊ณผ๋ฅผ ๊ด์ฐฐํ๋ฉด์ ์์ฐ ๋ฐฐ์ถ์ ๊ธฐ๋ํด ๋ณผ ์ ์๊ฒ ๋ค. ํนํ ๋์ ์ด๋ ๋ฐ๋๋๊ณผ ๊ฐ์ด ๋ฅ๊ทผ ๋ฌผ์ฒด๊ฐ ์๋๋ฅผ ํต๊ณผํ์ฌ ์ ๋๋ ๊ทธ ์ดํ์ ์์นํด ์๋ค๋ฉด ์์ฐ ๋ฐฐ์ถ์ ๊ฐ๋ฅ์ฑ์ด ๋์ผ๋ฏ๋ก ๊ธฐ๋ค๋ ค ๋ณด๋ ๊ฒ์ด ์ข๊ฒ ๋ค. ๋ค๋ง ๋์คํฌ ๋ฐฐํฐ๋ฆฌ์ ๊ฒฝ์ฐ๋ ์ฌ๋ฌ ๊ฐ์ง ํฉ๋ณ์ฆ์ ๊ณ ๋ คํ์ ๋ ๋ด์๊ฒฝ์ ์ ๊ฑฐ์ ์ ์ํํ๋ ๊ฒ์ด ์์ ํ ๊ฒ์ผ๋ก ์๊ฐ๋๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001081852
|
oai_dc
|
์ฅ์ค์ฒฉ์ฆ์ ์ด๋ํ ํ๋งน๋ถ์ MALT ๋ฆผํ์ข
1์
|
A Case of Intussusception Secondary to Ileocecal MALT Lymphoma
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ด์ํฌ(์กฐ์ ๋ํ๊ต); ์์์(์กฐ์ ๋ํ๊ต); ๋ฌธ๊ฒฝ๋(์กฐ์ ๋ํ๊ต)"
] |
์ ์๋ค์ ๋ง์ฑ ๋ณตํต๊ณผ ์ฒด์ค๊ฐ์๋ฅผ ํธ์ํ๋ 10์ธ ์ฌ์์์ ์ฅ์ค์ฒฉ์ฆ์ ์ด๋ํ ํ๋งน๋ถ์ ๋ฐ์ํ ์ ๋ฑ๊ธ MALT ๋ฆผํ์ข
1์๋ฅผ ๊ฒฝํํ์๊ธฐ์ ๋ฌธํ ๊ณ ์ฐฐ๊ณผ ํจ๊ป ๋ณด๊ณ ํ๋ ๋ฐ์ด๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001081855
|
oai_dc
|
์ ์ฒ์ฑ ํ๋ฆฌํค๋ฅด๋์ 1์
|
A Case of Congenital Lumbar Hernia
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ด๋ณ๊ธฐ(๋ถ์ฐ๋ํ๊ต); ๊นํด์(๋ถ์ฐ๋ํ๊ต); ์กฐ์ฉํ(๋ถ์ฐ๋ํ๊ต); ๋ฐ์ฌํ(๋ถ์ฐ๋ํ๊ต)"
] |
์ ์ฒ์ฑ ํ๋ฆฌํค๋ฅด๋์๋ 12๋ฒ ๋๊ณจ๊ณผ ์ฅ๊ณจ ์ฌ์ด์ ํ๋ณต๋ฒฝ ์์ธก๋ถ์ ๋ฐ์ํ๋ ํ์ฅ์ผ๋ก ๋งค์ฐ ๋๋ฌธ ์งํ์ด๋ค. ์ถ์ ์๋ถํฐ ์ฐ์ธก ์ธก๋ณต๋ถ์์ ๋ฉ์ด๊ฐ ๋ฐ๊ฒฌ๋์๊ณ ์ ์ฐจ ํฌ๊ธฐ๊ฐ ์ฆ๊ฐํ์ฌ ๋ด์ํ 4๊ฐ์ ๋ ๋จ์์์ ๋ณต๋ถ ์ด์ํ ๊ฒ์ฌ ๋ฐ ๋ณต๋ถ ์ ์ฐํ ๋จ์ธต ์ดฌ์์ผ๋ก ์ ์ฒ์ฑ ์๋ถ ํ๋ฆฌํค๋ฅด๋์๊ฐ ์ง๋จ๋์๊ณ ์ผ์ฐจ ๋ดํฉ์ ๋ก ์์น๋์๊ธฐ์ ๋ณด๊ณ ํ๋ ๋ฐ์ด๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001081853
|
oai_dc
|
๋ฐ๋ณต์ฑ ๋ณตํต์ผ๋ก ๋ฐํ๋ ๋ณต์ฑ ๊ฐ์ง 1์
|
A Case of Abdominal Epilepsy Presenting withRecurrent Abdominal Pain
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ก์ ์ค(๊ณ๋ช
๋ํ๊ต); ๊น์ค์(๊ณ๋ช
๋ํ๊ต); ํฉ์ง๋ณต(๊ณ๋ช
๋ํ๊ต)"
] |
์ ์๋ค์ 6์ธ ๋ ๋จ์์์ 4๋
๊ฐ์ ๋ฐ๋ณต์ ์ด๊ณ , ๋ฐ์์ ์ธ ๋ณตํต์ ์์ธ์ ๊ท๋ช
ํ๋ ์ค ๋ง์ฑ ๋ณตํต์ ํ ๊ธฐ์ง์ ์งํ๋ค์ด ๋ฐฐ์ ๋๊ณ , ๋ํ ๊ฒ์ฌ์ ์ด์ ์๊ฒฌ๊ณผ ํจ๊ป ํญ๊ฒฝ๋ จ์ ์ ์ฌ์ฉ์ ์ฆ์์ ๊ทน์ ์ธ ์์ค์ ๋ณด์ฌ ๋ณต์ฑ ๊ฐ์ง๋ก ์ง๋จ๋ 1์๋ฅผ ๊ฒฝํํ๊ณ ๋ฌธํ ๊ณ ์ฐฐ๊ณผ ํจ๊ป ๋ณด๊ณ ํ๋ ๋ฐ์ด๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001081661
|
oai_dc
|
์์์์ ๋ฐ์ํ ํํ์ฑ ์์ฅ๊ฒฐ์ฅ์ผ
|
Ischemic Enterocolitis in Children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ด๋ณ๊ธฐ(๋ถ์ฐ๋ํ๊ต); ๋ฐ์ฌํ(๋ถ์ฐ๋ํ๊ต)"
] |
๋ชฉ ์ : ํํ์ฑ ์์ฅ๊ฒฐ์ฅ์ผ์ ์์ฅ๊ณผ ๋์ฅ์ ์ฅ๋ฒฝ์ ์ก์์ ์ผ๋ก ๊ดด์ฌ ๋ฐ ๋๋ ๋ถ์ ๊ดด์ฌ๋ฅผ ๋ณด์ด๊ณ ํ๋ฏธ๊ฒฝ์ ์ผ๋ก๋ ์ ๋ง ๋ฐ ์ ๋งํ์ธต์ ํํ์ฑ ๋ณํ๋ฅผ ์ผ์ผํค๋ ๊ธ์ฑ ์งํ์ด๋ค. ๋ค์ํ ์์์ฆ์์ ๋ณด์ด๋ฉฐ ๋์ฆ ์น๋ฃ๋ก ํธ์ ๋๊ธฐ๋ ํ์ง๋ง ์ฅ๊ดด์ , ๋
์ํ์ฆ, ์ฌ๋ง ๋ฑ ์ค์ฆ ๊ฒฝ๊ณผ๋ฅผ ๋ฐ๊ธฐ๋ ํ๋ค. ์์ธ์ ํ์คํ ๋ฐํ์ง์ง ์์์ง๋ง ์ฅ ๋ฏธ์ธ์ํ์ ์ฅ์ ๋ ๊ณผ๋ฏผ๋ฐ์์ด ์ฃผ๋ ๋ณ๋ฆฌ ๊ธฐ์ ์ผ๋ก ์ค๋ช
๋๊ณ ์๋ค.๋ฐฉ ๋ฒ: ๋ถ์ฐ๋ํ๊ต๋ณ์ ์์๊ณผ์ ๋ณตํต, ํ๋ณ, ํ ํ, ๊ตฌํ ๋๋ ๋ณต๋ถํฝ๋ง ๋ฑ์ ๊ธ์ฑ ๋ณต์ฆ์ผ๋ก ๋ด์ํ ํ์ ์ค ๋ฐฉ์ฌ์ ๊ฒ์ฌ ์๊ฒฌ, ์์ ์๊ฒฌ, ๋ด์๊ฒฝ ์๊ฒฌ, ์กฐ์ง๋ณ๋ฆฌ ์๊ฒฌ ๋ฑ์ด ๊ดด์ฌ ๋ฐ ๋๋ ๋ถ์ ๊ดด์ฌ์ ์๊ฒฌ์ ๋ณด์ด๊ณ ์ฅ๊ฐ๋ง ๋๋งฅ์ ํ์์ ์๊ฒฌ์ด ์์ผ๋ฉฐ ์ฅ์ ํํ์ด๋ ๊ดด์ฌ์ ๋ค๋ฅธ ๊ธฐ๊ณ์ ๋๋ ์ ์ ์ ์์ธ์ด ์๋ ํํ์ฑ ์์ฅ๊ฒฐ์ฅ์ผ์ ํฉ๋นํ 6๋ช
์ ์์ ์๊ฒฌ์ ํํฅ์ ์ผ๋ก ๋ถ์ํ์๋ค.๊ฒฐ ๊ณผ: 1) ๋จ์๊ฐ 4๋ช
, ์ฌ์๊ฐ 2๋ช
์ด์๋ค. 2) ์ฐ๋ น ๋ถํฌ๋ ์ํ 6์ฃผ์์ 6์ธ๊น์ง์๋ค. 3) ๋ง์ญ์ ๊ฐ๊น์ด 1๋ช
์ ์ ์ธํ๊ณ ๋ชจ๋ ๋ง์ญ์์๊ณ ๋ถ๋น๊ฒฝ๋์ 1๋ช
์ ์ ์ธํ๊ณ ๋ ์ ์ ์ถ์ ์ฒด์ค์์๋ค. 4) ์ฆ์์ผ๋ก๋ ์ ํ๋ณ ๋๋ ํ ํ 5์, ๊ตฌํ , ์ค์ฌ, ๋ณตํต ๋๋ ๋ณด์ฑ์ด ๊ฐ๊ฐ 4์, ๋ณต๋ถํฝ๋ง๊ณผ ๋ฐ์ด 3์์๋ค. 5) ์นจ๋ฒ ๋ถ์๋ ํํ ๊ฒฐ์ฅ 2์, ํํ ๊ฒฐ์ฅ ๋ฐ S์ ๊ฒฐ์ฅ 1์, S์ ๊ฒฐ์ฅ 1์, ์ ๋์ฅ 1์, ์ญ์ด์ง์ฅ ๊ตฌ๋ถ ๋ฐ ์ ์ ๋ฌธ๋ถ๊ฐ 1์์๋ค. 6) ๋ณ๋ณ์ ํํ๋ ๊ถค์ 3์, ์ฒ๊ณต 2์, ๊ดด์ฌ ๋ฐ์ด 2์, ํ์ฐฉ 1์, ์ฌํ ๋ง์ฑ ์ํผ ํ๋ฝ 1์์๋ค. 7) ์น๋ฃ๋ก๋ ์ฒ๊ณต ๋ถ์์ ์ผ์ฐจ ๋ดํฉ 2์, ๋ณด์กด์ ์น๋ฃ(์์ก ์๋ฒ, ์ด ์ ๋งฅ ์์, ํญ์์ ํฌ์ฌ, ํ์คํ๋ฏผ ๊ธธํญ์ ํฌ์ฌ ๋ฑ) 4์์๋ค. 8) 1์์์ ๊ธ์ฑ ์ ๋ถ์ ์ด ๋๋ฐ๋์๊ณ ์ฌ๋ง์๋ ์์๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001081849
|
oai_dc
|
๋น๋ง์์์ ๋น์์ฝ์ฌ์ฑ ์ง๋ฐฉ๊ฐ์ผ์ ์ํ์์ธ
|
Risk Factors of Non-alcoholic Steatohepatitis in Childhood Obesity
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ค์์ค(์๋จ๋ํ๊ต); ๋ฐ์ฉํ(์๋จ๋ํ๊ต); ์ต๊ดํด(์๋จ๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART001081857
|
oai_dc
|
3์ธ ์ฌ์์์ ์ง๋จ๋ ํน๋ฐ์ฑ ๋ฌธ๋งฅ ๊ณ ํ์ 1์
|
A Case of Idiopathic Portal Hypertension in a 3-year-old Girl
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์๊ธฐ์(์ฐ์ธ๋ํ๊ต); ๋ฐฑ์น์ฐ(์ฐ์ธ๋ํ๊ต); ์ ๊ธฐ์ญ(์ฐ์ธ๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART001081851
|
oai_dc
|
์ฝ์ผ ์์ ์ ๋ก ์น๋ฃํ ์์ Dieulafoy ๋ณ๋ณ 1์
|
A Case of a Dieulafoy Lesion Treated usingCoil Embolization in a Child
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ ์ง๋ฏธ(์ธ์ ๋ํ๊ต); ์ก๋ฏผ์ญ(์ธ์ ๋ํ๊ต); ์ง๊ทผํ(์ธ์ ๋ํ๊ต); ๋ฐฐ์ฌ์ต(์์ฃผ๋ํ๊ต); ๋ฐ์คํ(์ธ์ ๋ํ๊ต)"
] |
์ ์๋ค์ ๋ด์๊ฒฝ์ ์ํผ๋คํ๋ฆฐ ๊ตญ์ ์ฃผ์
๋ฒ๊ณผ ์์ ์ ํ๊ด ๊ฒฐ์ฐฐ์ ํ์๋ ์ถํ์ด ์ฌ๋ฐ๋ Dieulafoy ๋ณ์ ๊ฐ์ง ํ์์์ ๋๋งฅ ์ฝ์ผ ์์ ์ ๋ก ์งํ๋ ์ฆ๋ก๋ฅผ ๋ฌธํ ๊ณ ์ฐฐ๊ณผ ํจ๊ป ๋ณด๊ณ ํ๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001081850
|
oai_dc
|
๋น๋ง์์ ๋น์์ฝ์ฌ์ฑ ์ง๋ฐฉ๊ฐ ๋ฐ๋ณ์ ์์ด Adipokine๊ณผ ์ฒด์ง๋ฐฉ๋ถํฌ ๋ฐ ์ธ์๋ฆฐ ์ ํญ์ฑ๊ณผ์ ์ฐ๊ด์ฑ์ ๋ํ ์ฐ๊ตฌ
|
The Role of Adipokines in the Pathogenesis of Non-alcoholic Fatty Liver Disease in Obese Children; the Relationship between Body Fat Distribution and Insulin Resistance
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ํ๋(์์ธ๋ํ๊ต); ๊ณ ์ฌ์(์์ธ๋ํ๊ต); ์์ ๊ธฐ(์์ธ๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART001081662
|
oai_dc
|
๋์คํฌ ์ ์ง๋ฅผ ์ผํจ ์์์์๋ด์๊ฒฝ์ ์ด๋ฌผ ์ ๊ฑฐ์ ์ ๋น๊ต
|
Comparison of Endoscopic Removal of Disk Batteries in Children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊น์ ์ฅ(๊ฒฝ๋ถ๋ํ๊ต); ํ์ํฌ(๊ฒฝ๋ถ๋ํ๊ต); ์ต๋ณํธ(๊ฒฝ๋ถ๋ํ๊ต); ์กฐ๋ฏผํจ(๊ฒฝ๋ถ๋ํ๊ต); ์ํ์(๋๊ตฌ๋ํ๊ต); ์ํด๋ฆฌ(๊ฒฝ๋ถ๋ํ๊ต); ์ถ๋ฏธ์ (๊ฒฝ๋ถ๋ํ๊ต); ํฉ์๊ฒฝ(๊ฒฝ๋ถ๋ํ๊ต); ๋ฐ์ ๋ฏผ(๊ฒฝ๋ถ๋ํ๊ต); ํ์์ง(๊ฒฝ๋ถ๋ํ๊ต); ์ฌ์์ง(๊ฒฝ๋ถ๋ํ๊ต)"
] |
Purpose: Any battery impacted in the esophagus must be removed urgently because of the possibility of serious complications such as perforation, fistula, and mediastinitis. The use of endoscopic procedures was compared to find the most rapid, effective, and safe method to remove disk batteries.Methods: The cases of 24 children (9 males, mean age, 1.5 years) that had accidentally ingested disk batteries were reviewed. The patients had visited the Department of Pediatrics, Kyungpook National University Hospital from July 1997 to June 2007 for the removal of disk batteries. Endoscopic removal was attempted using a retrieval net or a magnetic extractor with a balloon (condom). The procedure times for removing the ingested battery were compared.Results: Children that ingested batteries with a larger diameter (20 mm) had a greater chance to have esophageal impaction with serious injury, such as esophageal mucosal necrosis or ulcers, as compared to the ingestion of smaller diameter batteries (10 mm) (p๏ผ0.01). Endoscopic removal of disk batteries was attempted either using a retrieval net in 10 children or by using a magnetic extractor with a balloon in 6 children. Endoscopic removal using a retrieval net was more effective (mean procedure time: 1.5 min) as compared to using a magnetic extractor with a balloon (mean procedure time: 3.3 min) (p๏ผ0.05).Conclusion: Both procedures, either using a retrieval net or a magnetic extractor with a balloon were effective in removing ingested disk batteries. Based on our experience, an endoscopic procedure using a retrieval net was a more effective method for foreign body removal. (Korean J Pediatr Gastroenterol Nutr 2007; 10: 147 156)
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001081848
|
oai_dc
|
์์ ์์ฑ ์ผ๊ณผ์ฑ ๊ณ ์ธ์ฐ๋ถํดํจ์ํ์ฆ์์์์์ ๋ฐ ์์ฐ๊ฒฝ๊ณผ์ ๋ํ ๊ณ ์ฐฐ
|
Clinical Features and Natural Course of Benign Transient Hyperphosphatasemia in Children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ค๋์ฑ(์์ธ๋ํ๊ต); ํ์ฌ์ค(์์ธ๋ํ๊ต); ์ํ๋(์์ธ๋ํ๊ต); ์ฅ์ฃผ์(์์ธ๋ํ๊ต); ๊ณ ์ฌ์ฑ(์์ธ๋ํ๊ต); ์ต์ ์ฐ(์์ธ๋ํ๊ต); ์์ ๊ธฐ(์์ธ๋ํ๊ต)"
] |
๋ชฉ ์ : ํ๊ตญ์ธ ์์์์ ์์ฑ ์ผ๊ณผ์ฑ ๊ณ ์ธ์ฐ๋ถํดํจ์ํ์ฆ(Benign transient hyperphosphatasemia, BTH)์ ์์์ ํน์ง ๋ฐ ์์ฐ ๊ฒฝ๊ณผ๋ฅผ ์ดํด๋ณด๊ณ ์ ํ์๋ค.๋ฐฉ ๋ฒ: 2006๋
6์๋ถํฐ 2007๋
7์๊น์ง ๋ถ๋น์์ธ๋ํ๊ต๋ณ์ ์์๊ณผ๋ฅผ ๋ด์ํ ํ์ ์ค Kraut ๋ฑ์ ์ง๋จ๊ธฐ์ค์ ๋ฐ๋ผ BTH๋ก ์ง๋จ๋ 17๋ช
์ ์๋ฌด๊ธฐ๋ก๊ณผ ๊ฒ์ฌ๊ฒฐ๊ณผ๋ฅผ ํํฅ์ ์ผ๋ก ๋ถ์ํ์๋ค.๊ฒฐ ๊ณผ: ์ด 17๋ช
์ ํ์ ์ค ๋จ์๊ฐ 6๋ช
, ์ฌ์๊ฐ 11๋ช
์ด์์ผ๋ฉฐ, ์ฐ๋ น์ ํ๊ท 26.9 13.8๊ฐ์(๋ฒ์: 9 49๊ฐ์)์ด์๋ค. ๋๋ฐ๋ ์งํ์ผ๋ก๋ ๊ฐ์ผ์ฑ ์งํ์ด 52.9%๋ก ๊ฐ์ฅ ๋ง์๊ณ , ๊ณ์ ์ ์ผ๋ก 9์์์ 12์ ์ฌ์ด์ ๋ ๋์ ๋ฐ์๋ฅ ์ ๋ณด์๋ค. ์ฒซ ๋ด์ ์ ์ธก์ ํ ํ์ฒญ ALP๋ ํ๊ท 2500.2 1165.1 U/L์ด์๊ณ , ๋ชจ๋ ํ์์์ 7์ฃผ ๋ด์ ํ์ฒญ ALP๊ฐ ์ ์ ๋๋ ์ ์ ์ํ์น์ ๋ ๋ฐฐ ์ด๋ด๋ก ๊ฐ์ํ์๋ค. ALP isoenzyme ๊ฒ์ฌ๋ฅผ ์ํํ 7๋ช
์ ํ์ ์ค 3๋ช
์์ ๊ฐ ๋ถํ๊ณผ ๊ณจ ๋ถํ์ ์ฆ๊ฐ๊ฐ ์์๊ณ , 4๋ช
์ ๊ณจ ๋ถํ์ ์ฆ๊ฐ๋ง์ ๋ณด์๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001081856
|
oai_dc
|
์๊ฐ๋ฉด์ญ์ฑ ๋ง์ฑ ์ท์ฅ์ผ์ผ๋ก ์ง๋จ๋ ์์ 1์
|
A Case of A Case of Autoimmune Chronic Pancreatitis in a Child
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ต์ธ์(์ ์ฃผ ์์๋ณ์); ์ง์ํฌ(์ ์ฃผ ์์๋ณ์); ์ต๊ฒฝ๋จ(์ ์ฃผ ์์๋ณ์); ๊น๊ฒฝ๋ชจ(์ธ์ฐ๋ํ๊ต)"
] |
์ ์๋ค์ ์๊ฐ๋ฉด์ญ ์งํ์ด ์๋ ๊ฑด๊ฐํ ์์๊ฐ ํฉ๋ฌ์ ๋๋ฐํ์ง ์๋ ๊ธ์ฑ ๋ณตํต์ผ๋ก ๋ด์ํ์ฌ ํ์ฒญ amylase, lipase์ ์ง์์ ์ธ ์์น๊ณผ ํ์ฒญ IgG ์ฆ๊ฐ, ์๊ฐ ํญ์ฒด(ANA, ANCA) ์์ฑ, ๋ฐฉ์ฌ์ ์์์์ ์ท์ฅ ์ค์ง ์ข
๋์ ์ท์ฅ ๋ฏธ๋ถ ์ฃผ์ท๊ด์ ๋ถ๊ท์น์ ํ์ฐฉ์ผ๋ก ์๊ฐ๋ฉด์ญ์ฑ ๋ง์ฑ ์ท์ฅ์ผ์ผ๋ก ์ง๋จ๋ฐ๊ณ ์คํ
๋ก์ด๋์ azathioprine์ ๊ฒฝ๊ตฌ ๋ณต์ฉํ์์ผ๋ฉฐ ๋ฏธ๋ถ ์ฃผ์ท๊ด ํ์ฐฉ์ ํ์ ํ์ฅ์ ์ ์ํํ๊ณ ํ๋ณต๋ 1์๋ฅผ ๊ฒฝํํ์๊ธฐ์ ๋ณด๊ณ ํ๋ ๋ฐ์ด๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001081854
|
oai_dc
|
๋์๋ชจ์ธํฌ์ข
๋ฐ ๊ฐ์กฑ์ฑ ์ ์ข
์ฑ ์ฉ์ข
์ฆ์ผ๋ก ๋ฐํํTurcot ์ฆํ๊ตฐ 1์
|
Medulloblastoma and Familial Adenomatous Polyposis in a 24-year-oldFemale Patient: A Case Report of Turcot Syndrome
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ ์์ธ(์ฑ๊ท ๊ด๋ํ๊ต); ์์ ๋ฏผ(์ฑ๊ท ๊ด๋ํ๊ต); ์ด์งํ(์ฑ๊ท ๊ด๋ํ๊ต); ์ดํด์ (์ฑ๊ท ๊ด๋ํ๊ต); ์ด์งํ(ํ๋ฆผ๋ํ๊ต); ์ฑ๊ธฐ์
(์ฑ๊ท ๊ด๋ํ๊ต); ์กํ์ (์ฑ๊ท ๊ด๋ํ๊ต); ์ต์ฐํธ(์ฑ๊ท ๊ด๋ํ๊ต)"
] |
์ ์๋ค์ ์๋ชจ์ธํฌ์ข
์ด ์๋ 24์ธ ์ฌ์ ํ์์์ ๊ฐ์กฑ์ฑ ์ ์ข
์ฑ ์ฉ์ข
์ฆ์ด ๋๋ฐ๋ Tucot ์ฆํ๊ตฐ 1์๋ฅผ ๊ฒฝํํ์์ผ๋ฉฐ ๋ฌธํ๊ณ ์ฐฐ๊ณผ ํจ๊ป ๋ณด๊ณ ํ๋ ๋ฐ์ด๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART001081847
|
oai_dc
|
HBsAb์ HBcAb๊ฐ ์์ฑ์ธ ์ฅ๊ธฐ ๊ณต์ฌ์์ ๊ฐ์กฐ์ง์์ Hepatitis B Virus DNA์ ๋ฐํ
|
Detection of Hepatitis B Virus DNA in Liver Grafts Obtained from HBsAb and HBcAb Positive Organ Donors
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ ์ฐฝ์ฐ(์ธ์ฐ๋ํ๊ต); ์ฅ์ฃผ์(์ธ์ฐ๋ํ๊ต); ๊น๊ฒฝ๋ชจ(์ธ์ฐ๋ํ๊ต); ์ด์น๊ท(์ธ์ฐ๋ํ๊ต)"
] |
๋ชฉ ์ : ์ต๊ทผ HBsAb ๋ฐ HBcAb ์์ฑ์ธ ๊ณต์ฌ์์ ๊ฐ์ด์ํธ์ ์ด์ ๋ฐ์ ์ํ์์์ ์ ์ Bํ ๊ฐ์ผ์ด ๋ฐ์ํ๋ ๊ฒ์ด ๋ณด๊ณ ๋๊ณ ์์ผ๋ฉฐ, ์ ์๋ค๋ ์ฝ 40%์์ ์ ์ Bํ ๊ฐ์ผ์ด ๋ฐ์ํ๋ ๊ฒ์ ๋ณด๊ณ ํ์๋ค. ํ๊ตญ์ธ์์์ HBcAb ์์ฑ๋ฅ ์ 50%๊ฐ ๋๋ ๊ฒ์ผ๋ก ๋ณด๊ณ ํ๊ณ ์๋๋ฐ, ์ด๋ ์์ ๊ฐ์ด์์ ๊ฑธ๋ฆผ๋์ด ๋ ์ ์์ผ๋ฉฐ ์ ์๋ค์ ์ด๋ฅผ ์๋ฐฉํ๊ธฐ ์ํ ์ผํ์ผ๋ก์จ ๋ณธ ์ฐ๊ตฌ๋ฅผ ์ํํ์๋ค.๋ฐฉ ๋ฒ: 1997๋
11์๋ถํฐ 1998๋
11์๊น์ง 12๊ฐ์ ๋์ ์์ธ ์์ฐ๋ณ์์์ ์์ฒด ๊ฐ์ด์ ๊ณต์ฌ์๊ฐ ๊ณผ๊ฑฐ Bํ ๊ฐ์ผ๊ณผ Cํ ๊ฐ์ผ ๊ฐ์ผ์ ์ฆ๊ฑฐ๊ฐ ์์ผ๋ฉด์ HBsAg ์์ฑ์ด๋ฉด์ HBsAb ์์ฑ, HBcAb ์์ฑ์ธ ์ฑ์ธ ๊ณต์ฌ์ 6๋ช
์ ๋์์ผ๋ก ํ์๋ค. ๊ฐ์ด์ ์์ ์ ๋๊ฒฐ ์๊ฒ์ ์ํ์ฌ ์ฑ์ทจํ ์ ํธ์ ์ผ๋ถ๋ฅผ ๋ณด๊ดํ์ฌ ์คํ์ ์ฌ์ฉํ์๋ค. ๋๊ฒฐ ์ ํธ ์กฐ์ง์์ DNA๋ฅผ ๋ถ๋ฆฌํ์ฌ, HBV DNA์ ํ๋ฉด ๊ตฌ์ญ๊ณผ ํต์ฌ ๊ตฌ์ญ์ ๋ํ ์๋ฐ์ฒด๋ฅผ ์ด์ฉํ์ฌ ์ด์ค ์คํฉ ํจ์ ์ฐ์ ๋ฐ์์ ์ํํ์ฌ ๊ฒ์ฌ๋ฅผ ์ํํ์๋ค.๊ฒฐ ๊ณผ: ๊ณต์ฌ์ 6๋ช
์ ์กฐ์ง์์ ํ๋ฉด ๊ตฌ์ญ์ด ๋ชจ๋ ์์ฑ์ผ๋ก ๊ด์ฐฐ๋์์ผ๋ฉฐ, ํต์ฌ ๊ตฌ์ญ์ 4๋ช
์์ ์์ฑ์ผ๋ก ๊ด์ฐฐ๋์๋ค. ๊ทธ ์ค 4๋ช
์ ๊ฐ์ ์ด์๋ฐ์ ์์ ์ํ์๋ ๋ชจ๋ ์๋ฐฉ๋ฒ์ ์ํํ๋ฉด์, ์ ์ Bํ ๊ฐ์ผ์ ๋ฐ์์ ๊ด์ฐฐ๋์ง ์๊ณ ์๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART000868849
|
oai_dc
|
์์์์์ ๋ฐ์ํ Intestinal Neuronal Dysplasia
|
Intestinal Neuronal Dysplasia in Twins
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์์ธ์(์ธ์ ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852412
|
oai_dc
|
์๋ถ ์์ฅ๊ด ์ฆ์ธ๊ฐ ์๋ ์์์ ์์ญ์ด์ง์ฅ๋ณ๋ณ ๋ฐ Helicobacter pylori ๊ฐ์ผ
|
Helicobacter pylori Infection and Gastroduodenal Pathologyin Children with Upper Gastrointestinal Symptoms
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ค์๋(๊ฒฝ์์๋); ์ด๊ดํธ(๊ฒฝ์๋ํ๊ต); ์คํฌ์(๊ฒฝ์๋ํ๊ต)"
] |
๋ง์ฑ ๋ฐ๋ณต์ฑ ๋ณตํต, ์์ฌ ํ ์๋ณต๋ถ ๋ถ์พ๊ฐ, ์ฆ์ ๊ตฌํ ๋ ๊ตฌ์ญ์ง์ด ์๋ ์์๋ฅผ ๋์์ผ๋ก ์๋ด์๊ฒฝ์ ์ํํ์ฌ ์์ญ์ด์ง์ฅ ๋ณ๋ณ์ ํ์ธํ๊ณ , ์๊ฒ์ฒด๋ฅผ ์ด์ฉํ ์์ญ์ด์ง์ฅ ์กฐ์งํ์ ๊ฒ์ฌ์ H. pylori ๊ฒ์ถ ๊ทธ๋ฆฌ๊ณ ๋ฉด์ญ๋ธ๋กฏํ
์ ํตํด ํ์ฒญ ๋ด์ H. pylori ํน์ด ํญ์ฒด ์กด์ฌ๋ฅผ ํ์ธํ์ฌ ํ๊ตญ์์ ๊ด์ฐฐ๋๋ ์์์ ์์ฅ๊ด ์ฆ์ธ์ ์์ญ์ด์ง์ฅ๋ณ๋ณ ๋ฐ H. pylori ๊ฐ์ผ๊ณผ์ ๊ด๊ณ๋ฅผ ์กฐ์ฌํ๊ณ ์ ํ์๋ค. ๋ฐฉ ๋ฒ: 1990๋
6์๋ถํฐ 1991๋
4์๊น์ง ๊ฒฝ์๋ํ๊ต๋ณ์ ์์๊ณผ์์ ์๋ถ ์์ฅ๊ด ์ฆ์์ผ๋ก ์๋ด์๊ฒฝ์ ์ํ ๋ฐ์ 184๋ช
์ค ์ ์ ์ ๋ถ์์ ์๊ฒ์ด๋์๊ณ , ์์๋ถํดํจ์ ๊ฒ์ฌ, Warthin-Starry ์์ผ์ ํน์ Hematoxylin-Eosin ์ผ์์ผ๋ก ์กฐ์งํ์ ์์ H. pylori์ ์กด์ฌ์ ๋ฌด๋ฅผ ํ์ธํ ์ ์์๋ 107๋ช
์ ๋์์ผ๋ก ์์ญ์ด์ง์ฅ ์กฐ์งํ์ ๊ฒ์ฌ์ IgG ๋ฉด์ญ๋ธ๋กฏํ
์ ์ํ ํญ-H. pylori ํญ์ฒด ๋ณด์ ์ ๋ฌด๋ฅผ ํ์ธํ์๋ค. ๊ฒฐ ๊ณผ: 1) ๋์ ํ์ 107๋ช
์ค ๋จ์๊ฐ 61๋ช
(57%), ์ฌ์๊ฐ 46๋ช
(43%)์ด์์ผ๋ฉฐ, ์ฐ๋ น์ 2์ธ๋ถํฐ 15์ธ๊น์ง ๋ถํฌํ์๊ณ ํ๊ท ์ฐ๋ น์ 10.7์ธ๋ก์ 10์ธ์์ 15์ธ ์ฌ์ด๊ฐ ๊ฐ์ฅ ๋ง์๋ค. 2) ๋ด์๊ฒฝ์ 15%์์ ์์ถํ ๋ฐ์ , ์๊ถค์, ์ญ์ด์ง์ฅ๊ถค์, ์ญ์ด์ง์ฅ ๋ฏธ๋, ์ถํ์ฑ ์ญ์ด์ง์ฅ์ผ ๋ฑ์ด ๊ด์ฐฐ๋์๊ณ ๋๋ถ๋ถ์ ๋ค์ํ ์ ๋์ ์์ ๋ง ๋ฐ์ ์ด ๊ด์ฐฐ๋์๋ค. 3) 107๋ช
์ค 94๋ช
(88%)์์ ๊ฒฝ๋ ์ด์์ ์กฐ์งํ์ ๋ง์ฑ์์ผ์ด ์์์ผ๋ฉฐ, ์ญ์ด์ง์ฅ ์กฐ์ง์ด ๊ฒ์ฌ ๊ฐ๋ฅํ์๋ 99๋ช
์ ์์์ ๋ง์ฑ์ญ์ด์ง์ฅ์ผ์ด ์์๋ค. 4) ์์๋ถํดํจ์ ๊ฒ์ฌ๋ ์์์๋ 45%, ์ญ์ด์ง์ฅ์์๋ 25.6%์์ ์์ฑ์ผ๋ก ํ์ ๋์๋ค. H&E ์ผ์ ๊ฒ์ฌ์์ 38.7%, Warthin-Starry ์์ผ์ ๊ฒ์ฌ์์๋ 40%์์ HPLO ์์ฑ์ด์๋ค. ์ด ์ธ๊ฐ์ง ๊ฒ์ฌ ์ค 1๊ฐ ๊ฒ์ฌ์์ ์์ฑ์ธ ๊ฒฝ์ฐ์ธ ์กฐ์งํ์ H. pylori ์์ฑ์ 57%์ด์๋ค. 5) IgG ๋ฉด์ญ๋ธ๋กฏํ
์์ฑ์ 96%์ด์๋ค. 6) ์ฐ๋ น๊ตฐ๋ณ ์กฐ์งํ์ H. pylori ์์ฑ์ 0โผ4์ธ ๊ตฐ์์๋ 29%, 5โผ9์ธ ๊ตฐ์์๋ 41%, 10โผ15์ธ ๊ตฐ์์๋ 68%๋ก ์ฐ๋ น์ด ์ฆ๊ฐํ ์๋ก ์์ฑ๋ฅ ์ด ์ฆ๊ฐํ์์ผ๋, ์กฐ์งํ์ ๋ง์ฑ์์ผ ๋ฐ ๋ง์ฑ์ญ์ด์ง์ฅ์ผ ๋น๋์ ๋ฉด์ญ๋ธ๋กฏ ์์ฑ ๋น๋๋ ์ฐ๋ น๊ตฐ๋ณ ์ฐจ์ด๊ฐ ์์ด ๋์ ์์ฑ๋ฅ ์ ์ ์งํ์๋ค. ๊ฒฐ ๋ก : ์๋ถ ์์ฅ๊ด ์ฆ์ธ๊ฐ ์๋ ์์์ ๋๋ถ๋ถ์ ์กฐ์งํ์ ๋ง์ฑ์์ผ ๋ฐ ๋ง์ฑ์ญ์ด์ง์ฅ์ผ๊ณผ ๋์์ H. pylori์ ๋ํ ํน์ด IgG ํญ์ฒด๋ฅผ ๋ณด์ ํ๊ณ ์์๋ค.
|
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
|||
ART000852413
|
oai_dc
|
Helicobacter pylori feo B ์ ์ ์์ ๋คํ์ฑ๊ณผ ์ฒ ๊ฒฐํ์ฑ ๋นํ๊ณผ์ ๊ด๊ณ
|
Polymorphism of the Helicobacter pylori feoB Gene and ClinicalCorrelation with Iron-deficiency Anemia in Korea
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋ฏผ๊ธฐ์ด(์ฑ๊ท ๊ด๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000868845
|
oai_dc
|
3์ธ ์์์์ ํ ํ์ ์ฃผ์๋ก ๋ด์ํ ์์๋ ํ์ถ์ฆ 1๋ก
|
Prolapse Gastropathy Presenting with Hematemesisin a 3-year-old Child - A Case Report
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์กฐ์ง์ฑ(๊ฐ์ฒ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000868846
|
oai_dc
|
Dieulafoy ๋ณ๋ณ ์์์ ๋ด์๊ฒฝ์ ์น๋ฃ 1๋ก
|
Endoscopic Management with Ethanol Injection in aChild with Gastric Dieulafoy Lesion
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊นํ์ง(์ดํ์ฌ์๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000868847
|
oai_dc
|
์์ ๋ง์ฑ ์ ๋ถ์ ํ์์์ ๋ฐ์ํ ์ํ๊ด ์ดํ์ฑ์ฆ์ Hemoclipping์ ์ํ์งํ ์น๋ฃ 1๋ก
|
Angiodysplasia in a Child with Chronic Renal Failure:Endoscopic Hemostatic Therapy
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ด์ค์ง(๋ถ์ฐ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000868848
|
oai_dc
|
์ ์์ ์ ๊ธฐํ์ข
1๋ก
|
Gastric Teratoma in a Newborn Infant; A Case Report
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์กฐ์งํ(๋์๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000868850
|
oai_dc
|
๋จ๋ฐฑ ์์ค ์ฅ์ฆ์ผ๋ก ๋ฐํํ ์ฐ์์ฑ ์ฉ์ข
์ฆ 1๋ก
|
A case of juvenile polyposis presented with protein losing entropathy
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊ฐ๋ณด์(์ธํ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000868851
|
oai_dc
|
์ํ 3๊ฐ์๋ถํฐ ์ฑ์ฅ์ฅ์ ๋ฅผ ๋ณด์ด๊ธฐ ์์ํ ๊ฐ๋ ์ฆํ๊ตฐ(Diencephalic Syndrome) 1๋ก
|
A Case of Diencephalic Syndrome Presented as Failure toThrive from Three Month of Age
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊น์น์(์์ฒํฅ๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000868773
|
oai_dc
|
Rotavirus ๊ฐ์ผ์ ์ฐ๋๋ณ ์ ํ์๊ธฐ์ ๋ณ๋์์ ๋ฐ ๊ธฐํ์์์ PM10๊ณผ์ ๊ด๊ณ
|
Influence of Climate Factors and PM10 on Rotaviral Infection:A Seasonal Variation Study
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ํ๋ผ(๊ฐ์ฒ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000868774
|
oai_dc
|
๋น์๋ณ ์ 1ํ์ ์ฅ๊ธฐ ์ถ์ ๊ด์ฐฐ; ๊ฐ์ ์ข
๋ฐ์์ ์ํ์์ธ์ ๋ํ ์ฐ๊ตฌ
|
Long-term Outcome of Glycogen Storage Disease Type 1;Analysis of Risk Factors for Hepatic Adenoma
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ํ๋(์์ธ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000868775
|
oai_dc
|
๋ง์ฑBํ๊ฐ์ผ ํ์์ ๋ํ Interferon-alfa์น๋ฃ๊ฒฐ๊ณผ์ ์ฅ๊ธฐ ์ถ์ ๊ด์ฐฐ
|
Long Term Follow Up of Interferon-alpha Treatment in Childrenwith Chronic Hepatitis B
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋ฐฑ์น์ฐ(์ฐ์ธ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000868841
|
oai_dc
|
์์ ๋ง์ฑBํ๊ฐ์ผ ํ์์ ๋ํ Interferon-alfa์ ์ฉ๋ ์ฐจ์ด ๋ฐ ์ฌ์น๋ฃ์ ๋ฐ๋ฅธ ์น๋ฃ ํจ๊ณผ ๋น๊ต
|
The Comparison of Interferon-ฮฑ Treatment by Dosages and Retreatmentfor Chronic Hepatitis B in Children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ฅ์ฐฝํ(๊ฒฝ๋ถ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000868842
|
oai_dc
|
์์จ๋ณ ํ์์์ ์ดํ ์ ํฉ ๋ณด์ธ์ ๊ณต์ฌ๊ฐ์ ์ด์ฉํ ํ์ฐ๊ฐ ์์ฒด ๋ถ๋ถ ๊ฐ์ด์
|
Living-Related Liver Transplantation with Heterozygote CarrierGraft in Children with Wilson Disease
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊น์งํ(์ธ์ฐ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000868843
|
oai_dc
|
์์๋ถ์ง์ด ์๋ 4์ธ ์ดํ ์.์ ์์ ์์ด ์ต๊ด์ ๋ํ ์กฐ์ฌ
|
Eating Habits of Children Under 4 Years with Poor-Feeding
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ค์ํ(์กฐ์ ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000868844
|
oai_dc
|
๋น๋ง์์์ ์ง๋ฐฉ๊ฐ์ ์์ธก ์ธ์๋ก์ ํ์ฒญ Aminotransferase์ ์์์ ์ ์ฉ์ฑ
|
The Clinical Usefulness of Serum Aminotransferase Activities forPredicting Fatty Liver in Obese Children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์์ ์
(์ ์ฃผ์์๋ณ์)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852388
|
oai_dc
|
์์์ ์์ฅ๊ด ์ด๋ฌผ์ ๋ํ ๊ณ ์ฐฐ
|
Gastrointestinal Foreign Bodies : Review of 96 Cases
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ด๋ฏผํ(๊ฒฝ์์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852392
|
oai_dc
|
ํ๋๊ธฐ ์์์์ ๋ฐ๋ณต์ฑ ๋ณตํต๊ณผ ์ฐ์ธ ์ฑํฅ๊ณผ์ ๊ด๊ณ
|
The Relationship between recurrent abdominal pain and depressive trends in school-aged children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์์์ค(์๋จ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852398
|
oai_dc
|
์์จ๋ณ ํ์์์ D-penicillamine ์น๋ฃ ์ค ๋ฐ์ํ ๋ฏธ์ธ๋ณํํ ์ ์ฆํ๊ตฐ 1๋ก
|
A Case of Minimal Change Nephrotic Syndrome Associated with D-penicillamine Therapy of Wilson`s Disease
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ค๊ธฐ์(๊ฒฝ๋ถ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852387
|
oai_dc
|
Helicobacter pylori ๊ฐ์ผ๊ณผ ์ฒ ๊ฒฐํ์ ๊ด๊ณ: 937๋ช
์ ์ฌ์ถ๊ธฐ ํ์์ ํ์ฒญ ์ ๋ณ๋ฅ ์ฐ๊ตฌ
|
The Relationship Helicobacter pylori Infection and Iron-Deficiency:Seroprevalence Study in 937 Pubscent Children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊น์์ข
(์ฑ๊ท ๊ด๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852389
|
oai_dc
|
์์ Clostridium Difficile ์ฅ์ผ๊ณผ ๊ด๋ จ๋ ํญ์์ ์ ๋ํ ์ฐ๊ตฌ
|
Clostiridium Difficile Colitis in childhood : associated antibiotics
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊น๋ณ์ฐฌ(์์ธ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852390
|
oai_dc
|
์์์์ ๋น์ฅํฐํธ์ค์ฑ ์ด๋ชจ๋ฌ๋ผ ์์ฅ๊ด์ผ์ ์์์์๊ณผ ํญ์์ ๋ด์ฑ๋ฅ ์ ๋ํ ์ฐ๊ตฌ
|
Non-typhodial salmonella Gastrointestinal in childhood : clinical features and antibiotics resistance
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๋์์(์์ธ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852391
|
oai_dc
|
์์ ๊ธ์ฑ ์ถฉ์๋๊ธฐ์ผ ์ง๋จ์ ์ง์ฐ์ ์ผ์ผํค๋ ์์ธ์ ๊ดํ ์ฐ๊ตฌ
|
Factors for delayed diagnosis of acute appendicitics in children
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"ํ๋ช
๊ธฐ(์ธ์ฐ๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852393
|
oai_dc
|
์ด์ ๋งฅ์์๋ฒ์ ๊ฐ๋ด๋ ํฉ๋ณ์ฆ์ ๋ํ Ursodeoxycholic Acid ์กฐ๊ธฐํฌ์ฌ์ ์ด์ค๋งน๊ฒ ์์ฝ๋์กฐ๊ตฐ ์ฐ๊ตฌ
|
A randomized, double-blind, placebo-controlled trial of early ursodeoxycholic acid administration for prevention of total parenteral nutrition-induced hepatobiliary complications
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ต์ฐํธ(์ฑ๊ท ๊ด๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852394
|
oai_dc
|
์ธ๊ณผ์ ๋ณต๋ถ์งํ์ผ๋ก ์ค์ธ๋ ๊ฒฐํต์ฑ ๋ณต๋ง์ผ 1๋ก
|
A case of tuberculous peritonitis mimicking surgical abdomem
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊นํ์ง(์ดํ์ฌ์๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852395
|
oai_dc
|
์์์์ ๊ฐ๋ด๋ ์ค์บ์ผ๋ก ์ง๋จ๋ ์ด ๋ด๊ด๋ญ์ ์์ฐ ์ฒ๊ณต์ ์ํ ๋ด์ฆ์ฑ ๋ณต๋ง์ผ 1๋ก
|
Bile peritonitis due to spontaneous rupture of choledochal cyst diagnosed by hepatobiliary scintigraphy in an infact
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊น์ข
์(๋ถ์ฐ๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852396
|
oai_dc
|
Alagille ์ฆํ๊ตฐ 1๋ก
|
a case of alagille syndrome
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"๊น์์(๊ณ๋ช
๋ํ๊ต)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000852397
|
oai_dc
|
์ ์ฒ์ฑ ๋ํ์์ฒด ๊ธฐ๋ฅ์ ํ์ฆ๊ณผ ๋๋ฐ๋ ์ ์์ ๋ด์ฆ์ ์ฒด 1๋ก
|
Neonatal cholestasis associated with congenital hypopiyuitarism
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ํ๋(์์ธ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000851238
|
oai_dc
|
์ง์ฅ์ ๋ฐ์ํ ์ฌ์ฌ์ฑ ๋ญ์ฑ ๋์ฅ์ผ(Colitis Cystica Profunda) ๋ฐ ์ฐ์์ฑ ์ ๋ฅ ์ฉ์ข
(Juvenile Retention Polyp)์ ํผ์ฌํ 1๋ก
|
A Case of Colitis Cystica Profunda Mixed with JuvenileRetention Polyp in a 7-month-old Infant
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ด์ฐฝ์ง(์์ธ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
||||
ART000851231
|
oai_dc
|
์์์์ ํธ๊ธฐ๋ด ์์๊ฒ์ฌ๋ฅผ ์ด์ฉํ ์ ๋น ํก์์ฅ์ ์ ๋ณ๋ฅ
|
Prevalence of Lactose Malabsorption in Children by Breath Hydrogen Test
|
{
"journal_name": "๋ํ์์์ํ๊ธฐ์์ํํ",
"publisher": null,
"pub_year": null,
"pub_month": null,
"volume": null,
"issue": null
}
|
[
"์ ์ฃผ์(์์ธ์๋)"
] |
์์๊ณผํ
| null |
kci_detailed_000004.xml
|
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