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| # Basal Cell Carcinoma (bcc) | |
| Source: DermNet NZ (dermnetnz.org) | |
| ## Source: https://dermnetnz.org/topics/basal-cell-carcinoma | |
| Authors: Honorary Associate Professor Amanda Oakley, Dermatologist, New Zealand (1997); Minor update: Dr Anthony Martin Fuentes, General Practitioner and Cosmetic Doctor, Hospital Jose Molina Orosa, Spain (2025) Update peer reviewed by: Dr Andjela Arandjelovic, Dermatology Clinical and Trials Research Fellow, Royal Melbourne Hospital, Australia (2025) | |
| Reviewing dermatologist: Dr Ian Coulson Edited by the DermNet content department. | |
| Introduction Demographics Causes Clinical features Types of BCC Complications Diagnosis Treatment for primary basal cell carcinoma Treatment for advanced basal cell carcinoma Prevention Outlook | |
| Basal cell carcinoma (BCC) is a common, locally invasive , keratinocyte cancer (also known as nonmelanoma cancer ). It is the most common form of skin cancer . BCC is also known as rodent ulcer and basalioma. Patients with BCC often develop multiple primary tumours over time. | |
| BCC is also known as rodent ulcer and basalioma. | |
| Age and sex : BCCs are particularly prevalent in elderly males. However, they also affect females and younger adults | |
| Previous BCC or other form of skin cancer ( squamous cell carcinoma , melanoma ) | |
| Sun damage ( photoageing , actinic keratoses ) | |
| Fair skin, blue eyes and blond or red hair — note; BCC can also affect darker skin types | |
| Previous cutaneous injury, thermal burn , disease (eg cutaneous lupus , sebaceous naevus ) | |
| Inherited syndromes: BCC is a particular problem for families with basal cell naevus syndrome ( Gorlin syndrome ), Bazex-Dupré-Christol syndrome , Rombo syndrome, Oley syndrome and xeroderma pigmentosum | |
| Other risk factors include ionising radiation, exposure to arsenic , immune suppression due to disease or medicines , and use of some other medicines such as hydrochlorothiazide. | |
| Most often, there are DNA mutations in the patched (PTCH) tumour suppressor gene , part of the hedgehog signalling pathway. | |
| These may be triggered by exposure to ultraviolet radiation . | |
| Various spontaneous and inherited gene defects predispose to BCC. | |
| What are the clinical features of basal cell carcinoma? | |
| BCC is a locally invasive skin tumour. The main characteristics are: | |
| Varies in size from a few millimetres to several centimetres in diameter | |
| BCC is very rarely a threat to life. A tiny proportion of BCCs grow rapidly, invade deeply, and/or metastasise to local lymph nodes. | |
| See also: Basal cell carcinoma in skin of colour | |
| There are several distinct clinical types of BCC, and over 20 histological growth patterns of BCC. | |
| Shiny or pearly nodule with a smooth surface | |
| May have central depression or ulceration, so its edges appear rolled | |
| Cystic variant is soft, with jelly-like contents | |
| Micronodular, microcystic and infiltrative types are potentially aggressive subtypes | |
| Most common type on the upper trunk and shoulders | |
| Waxy, scar-like plaque with indistinct borders | |
| May infiltrate cutaneous nerves ( perineural spread) | |
| Also known as morpheic, morphoeiform or sclerosing BCC | |
| Mixed basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) | |
| Potentially more aggressive than other forms of BCC | |
| Also known as basosquamous carcinoma and mixed basal- squamous cell carcinoma | |
| What are the complications of basal cell carcinoma? | |
| Recurrence of BCC after initial treatment is not uncommon. Characteristics of recurrent BCC often include: | |
| Incomplete excision or narrow margins at primary excision | |
| Morphoeic, micronodular, and infiltrative subtypes | |
| Advanced BCCs are large, often neglected tumours. | |
| They may be several centimetres in diameter | |
| They may be deeply infiltrating into tissues below the skin | |
| They are difficult or impossible to treat surgically | |
| Primary tumour is often large, neglected or recurrent, located on head and neck, with aggressive subtype | |
| May arise in-site exposed to ionising radiation | |
| BCC is diagnosed clinically by the presence of a slowly enlarging skin lesion with typical appearance. | |
| Arborizing vessels ( telangiectasia with tree-like branching) | |
| Additional criteria for non-pigmented, superficial BCC: | |
| Non-classical vascular patterns (hairpin, glomerular, dotted, comma). | |
| Shiny white lines — tend to be disorganised or arranged in parallel | |
| Stellate pattern — from the visible tumour edge; may be formed by white lines, vessels, or uneven skin surfaces | |
| Multiple aggregated yellow-white (MAY) globules. | |
| The diagnosis and histological subtype is usually confirmed pathologically by a diagnostic biopsy or following excision . See: basal cell carcinoma pathology . | |
| While histology remains the gold standard for BCC subtyping, non-invasive optical techniques like line-field confocal optical coherence tomography (LC-OCT) are increasingly utilized for BCC diagnosis and monitoring. LC-OCT has proven its effectiveness in real-world settings, enabling early detection, minimizing unnecessary biopsies , and providing valuable insights into disease progression, especially in cases where surgery is not indicated. | |
| What is the treatment for primary basal cell carcinoma? | |
| The treatment for a BCC depends on its type, size and location, the number to be treated, patient factors, and the preference or expertise of the doctor. Most BCCs are treated surgically. Long-term follow-up is recommended to check for new lesions and recurrence; the latter may be unnecessary if histology has reported wide clear margins. | |
| Excision means the lesion is cut out and the skin stitched up. | |
| Most appropriate treatment for nodular, infiltrative and morphoeic BCCs. | |
| Should include 3 to 5 mm margin of normal skin around the tumour. | |
| Very large lesions may require flap or skin graft to repair the defect. | |
| A pathologist will report deep and lateral margins. | |
| Further surgery is recommended for lesions that are incompletely excised. | |
| Mohs micrographically controlled excision | |
| Mohs micrographically controlled surgery involves examining carefully marked excised tissue under the microscope , layer by layer, to ensure complete excision. | |
| Very high cure rates achieved by trained Mohs surgeons. | |
| Used in high-risk areas of the face around eyes, lips, and nose. | |
| Suitable for ill-defined, morphoeic, infiltrative and recurrent subtypes. | |
| Large defects are repaired by flap or skin graft . | |
| Superficial skin surgery comprises shave, curettage , and electrocautery . It is a rapid technique using local anaesthesia and does not require sutures . | |
| Suitable for small, well-defined nodular or superficial BCCs. | |
| Lesions are usually located on the trunk or limbs. | |
| Wound is left open to heal by secondary intention . | |
| Moist wound dressings lead to healing within a few weeks. | |
| Cryotherapy is the treatment of a superficial skin lesion by freezing it, usually with liquid nitrogen. | |
| Suitable for small superficial BCCs on covered areas of the trunk and limbs. | |
| Best avoided for BCCs on head and neck, and distal to knees. | |
| Results in a blister that crusts over and heals within several weeks. | |
| Photodynamic therapy (PDT) refers to a technique in which BCC is treated with a photosensitising chemical, and exposed to light several hours later. | |
| Topical photosensitisers include aminolevulinic acid lotion and methyl aminolevulinate cream . | |
| Suitable for low-risk small, superficial BCCs. | |
| Best avoided if tumour in-site at high risk of recurrence. | |
| Results in inflammatory reaction, maximal 3–4 days after procedure. | |
| Treatment repeated 7 days after initial treatment. | |
| Imiquimod is an immune response modifier. | |
| Best used for superficial BCCs less than 2 cm diameter. | |
| Applied three to five times each week, for 6–16 weeks. | |
| Results in a variable inflammatory reaction, maximal at three weeks. | |
| 5-Fluorouracil cream is a topical cytotoxic agent. | |
| Used to treat small superficial basal cell carcinomas. | |
| Requires prolonged course, eg twice daily for 6–12 weeks. | |
| Radiotherapy or X-ray treatment can be used to treat primary BCCs or as adjunctive treatment if margins are incomplete. | |
| Best avoided in young patients and in genetic conditions predisposing to skin cancer. | |
| Best cosmetic results achieved using multiple fractions. | |
| Typically, patient attends once-weekly for several weeks. | |
| Causes inflammatory reaction followed by scar. | |
| Risk of radiodermatitis , late recurrence, and new tumours. | |
| What is the treatment for advanced or metastatic basal cell carcinoma? | |
| Locally advanced primary, recurrent or metastatic BCC requires multidisciplinary consultation. Often a combination of treatments is used. | |
| Targeted therapy refers to the hedgehog signalling pathway inhibitors , vismodegib and sonidegib . These drugs have some important risks and side effects. | |
| How can basal cell carcinoma be prevented? | |
| The most important way to prevent BCC is to avoid sunburn . This is especially important in childhood and early life. Fair-skinned individuals and those with a personal or family history of BCC should protect their skin from sun exposure daily, year-round and lifelong. | |
| Stay indoors or under the shade in the middle of the day. | |
| Apply high protection factor SPF50+ broad-spectrum sunscreens generously to exposed skin if outdoors. | |
| Oral nicotinamide (vitamin B3) in a dose of 500 mg twice daily may reduce the number and severity of BCCs. | |
| What is the outlook for basal cell carcinoma? | |
| Most BCCs are cured by treatment. Cure is most likely if treatment is undertaken when the lesion is small. | |
| About 50% of people with BCC develop a second one within 3 years of the first. They are also at increased risk of other skin cancers , especially melanoma . Regular self-skin examinations and long-term annual skin checks by an experienced health professional are recommended. | |
| Álvarez-Salafranca M, Ara M, Zaballos P. Dermoscopy in Basal Cell Carcinoma: An Updated Review. Advances in Dermatology. 2021; doi: 10.1016/j.ad.2020.11.011. Journal | |
| Barbarossa L, D’Onghia M, Cartocci A, Suppa M, Tognetti L, Cappilli S, Peris K, Perez-Anker J, Malvehy J, Baldino G, et al. Understanding the Dermoscopic Patterns of Basal Cell Carcinoma Using Line-Field Confocal Tomography. Tomography. 2024; 10(6):826-838. https://doi.org/10.3390/tomography10060063. Journal | |
| Kim DP, Kus KJB, Ruiz E. Basal Cell Carcinoma Review. Head & Neck Oncology. 2018;10(1):21. doi: 10.1016/j.hoc.2018.09.004. Journal | |
| Menzies SW, Westerhoff K, Rabinovitz H, Kopf AW, McCarthy WH, Katz B. Surface Microscopy of Pigmented Basal Cell Carcinoma. Arch Dermatol. 2000;136(8):1012–1016. doi:10.1001/archderm.136.8.1012. Journal | |
| Wojtowicz I, Żychowska M. Dermoscopy of Basal Cell Carcinoma Part 1: Dermoscopic Findings and Diagnostic Accuracy-A Systematic Literature Review. Cancers (Basel). 2025;17(3):493. Published 2025 Feb 1. doi:10.3390/cancers17030493. Journal | |
| Work Group; Kim JYS, Kozlow JH, Mittal B, Moyer J, Olencki T, Rodgers P. Guidelines of care for the management of basal cell carcinoma. J Am Acad Dermatol. 2018;78(3):540-559. doi: 10.1016/j.jaad.2017.10.006. Journal | |
| Basal cell carcinoma — common skin lesions course | Basal cell carcinoma dermoscopy | Genetics of basal cell carcinoma | Basal cell carcinoma pathology | Basal cell carcinoma in skin of colour | |
| Dermatological procedures | Mohs micrographic surgery | Targeted cancer therapy | |
| Skin cancer | Skin lesions | Vulval cancer | |
| Skin cancers and precancers — DermNet e-lecture [Youtube] | |
| Clinical practice guidelines for keratinocyte cancer — Cancer Guidelines wiki | |
| American College of Mohs Micrographic Surgery and Oncology | |
| Mohs Micrographic Surgery from Johns Hopkins Oncology Center | |
| Basal cell carcinoma : emedicine dermatology, the online medical reference textbook. | |
| Basal cell carcinoma — British Association of Dermatologists | |
| Optimal care pathway for people with basal cell carcinoma or squamous cell carcinoma — Cancer Council of Australia, June 2016 | |
| Basal cell carcinoma — American Academy of Dermatology |