Mélanome malin
Central nervous system and mucosal
Revu par Dr Hayley Willacy, FRCGP Dernière mise à jour par Dr Philippa Vincent, MRCGPLast updated 20 Nov 2021
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Professionnels de la santé
Professional Reference articles are designed for health professionals to use. They are written by UK doctors and based on research evidence, UK and European Guidelines. You may find the Cancer de la peau mélanome article more useful, or one of our other articles de santé.
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What is malignant melanoma?
Cancerous growth of melanocytes results in melanoma. 90% of melanomas are cutaneous but malignant melanomas have been described in nearly every organ of the body. Non-cutaneous melanomas are rare.1
Malignant melanoma of skin (cutaneous malignant melanoma)
Retour au sommaireSee the separate Malignant melanoma of skin article.
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Choroidal melanoma
Retour au sommaireSee the separate Choroidal melanoma article.
Melanoma of the central nervous system
Retour au sommaireThe most common form of melanoma in the central nervous system (CNS) is metastases of cutaneous melanoma. Melanoma has the highest risk of spread to the CNS among all common cancer types. More than 60% of patients with malignant melanoma will develop brain metastases, with higher risks if the primary tumour was on the head, neck or trunk, the BRAF mutation is present (present in 40% of malignant melanomas), 2 the primary tumour was deep, ulcerated or invasive or where the melanoma also has metastasised to other organs. 3
Brain metastases due to malignant melanoma most commonly present with headaches (40-50%) whilst 20-40% present with focal neurological symptoms.2
Prior to 2000, the prognosis for brain metastases arising from malignant melanoma was poor with a 3-4 month mean survival and a one-year survival of < 10%. This has improved with developments in radiotherapy and immunotherapy. One-year survival is now around 50% and two-year survival around 27%.2
Primary intracranial malignant melanoma (PIMM) arise from leptomeningeal melanocytes.
Primary intracranial melanomas account for 1% of all malignant melanomas and 0.07% of intracranial tumours. 4
Prognosis for primary intracranial melanoma is poor with a mean survival of 22 months. 5
There is limited evidence for treatment for primary intracranial melanomas. Currently radical resection with radiotherapy possibly increases survival but targeted immunotherapy is likely to offer the most hope in the future. 5
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Mucosal melanoma 6
Retour au sommaireMucosal melanoma present in the anorectum, nasal cavity, genitourinary tract, upper gastrointestinal tract and maxillary sinus.
Mucosal melanomas make up 1% of all malignant melanomas.
Risk factors are less well known but include cigarette smoking, denture irritation, alcohol, chronic infections caused by microorganisms and mechanical stress generated by routine activities.
They tend to be aggressive with a poorer prognosis than cutaneous malignant melanomas (10-20% 5-year survival compared with 93% for cutaneous).
One of the reasons for this is that they tend to be diagnosed at a later stage. 7
Radical tumour excision remains the first line treatment. 8
Targeted immunotherapy is likely to be the most successful treatment but, to date, mucosal melanomas are showing a lower response than cutaneous melanomas. 8
Melanoma of unknown primary site (MUP)
Retour au sommaireVoir également le document séparé Carcinomatose article.
No primary lesion is identified in 3% of patients presenting with palpable evidence of regional metastatic melanoma.9
Patients with occult primary melanoma may present with a solitary metastasis, lymph node disease, or systemic disease. It is diagnosed when, despite thorough physical examination and revision of previous histology, no primary cutaneous, ocular, or mucosal melanoma can be found.9
All patients should be staged. MUP is classified as stage III when lymph node or skin/subcutaneous metastases are present and as stage IV when there is visceral involvement. 10
Immunotherapy and targeted therapy have improved the prognosis but it remains difficult to predict efficacy. 10
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Lectures complémentaires et références
- Melanoma: assessment and management; NICE Guidance (July 2015 - last updated July 2022)
- Del Prete V, Chaloupka K, Holzmann D, et al; Noncutaneous Melanomas: A Single-Center Analysis. Dermatology. 2016;232(1):22-9. doi: 10.1159/000441444. Epub 2015 Dec 1.
- Lekkala MR, Mullangi S; Malignant Melanoma Metastatic to the Central Nervous System.
- Brain Metastases; At Melanoma Foundation
- A case report and literature review on primary intracranial malignant melanoma: Challenges and insights; W Saleem et al; International Journal of Surgery Case Reports
- Chen L, Yang Y, Li D, et al; Primary intracranial malignant melanomas: A case series with literature review. Medicine (Baltimore). 2024 Nov 1;103(44):e40334. doi: 10.1097/MD.0000000000040334.
- Mucosal Melanoma: Pathological Evolution, Pathway Dependency and Targeted Therapy; Y Ma et al: Frontiers in Oncology
- Santeufemia DA, Palmieri G, Miolo G, et al; Current Trends in Mucosal Melanomas: An Overview. Cancers (Basel). 2023 Feb 21;15(5):1356. doi: 10.3390/cancers15051356.
- Sergi MC, Filoni E, Triggiano G, et al; Mucosal Melanoma: Epidemiology, Clinical Features, and Treatment. Curr Oncol Rep. 2023 Nov;25(11):1247-1258. doi: 10.1007/s11912-023-01453-x. Epub 2023 Sep 29.
- Melanoma of Unknown Primary: Evaluation of the Characteristics, Treatment Strategies, Prognostic Factors in a Monocentric Retrospective Study; P Del Fiore et al; Frontiers in Oncology
- Melanoma of unknown primary: a comprehensive review of immune-mediated pathogenesis and therapies; W Xu; The Oncologist
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About the authorView full bio

Dr Philippa Vincent, MRCGP
Médecin généraliste, Auteur médical
MB BS, Bsc, MRCGP (2000), DCH, DFSRH, DRCOG
Dr Philippa Vincent is an NHS GP working in North London.
About the reviewerView full bio

Dr Hayley Willacy, FRCGP
Médecin généraliste, Auteur médical
MBChB (1992), DRCOG, DFFP, MRCOG (Part 1) MRCGP (2007), DFSRH (2013), MSc - medical education (2020)
Dr Hayley Willacy was an NHS GP working in northwest England, who retired from clinical practice in 2022 after 30 years.
Historique de l'article
Les informations sur cette page sont rédigées et examinées par des cliniciens qualifiés.
Next review due: 19 Nov 2026
20 Nov 2021 | Dernière version

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