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Neurotropic Melanoma: The Management of Localised Disease

Neurotropic melanoma is a rare subtype of cutaneous malignant melanoma. Compared with conventional melanoma, it is more locally aggressive with an increased tendency for local recurrence but less likely for nodal or distant metastases. These tumours can be a diagnostic dilemma with a variety of morp...

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Detalles Bibliográficos
Autores principales: Croker, Jeremy, Burmeister, Bryan, Foote, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3486009/
https://www.ncbi.nlm.nih.gov/pubmed/23133758
http://dx.doi.org/10.1155/2012/706452
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author Croker, Jeremy
Burmeister, Bryan
Foote, Matthew
author_facet Croker, Jeremy
Burmeister, Bryan
Foote, Matthew
author_sort Croker, Jeremy
collection PubMed
description Neurotropic melanoma is a rare subtype of cutaneous malignant melanoma. Compared with conventional melanoma, it is more locally aggressive with an increased tendency for local recurrence but less likely for nodal or distant metastases. These tumours can be a diagnostic dilemma with a variety of morphological, histopathological, and immunophenotypical expressions. The often amelanotic, benign appearance may lead to treatment issues such as late presentation, diagnostic delay, misdiagnosis, insufficient surgical margins, and recurrence with resulting poor outcome. The neurotropic nature of the disease and prevalence in the head and neck region can result in perineural and neural invasion along named large nerves into the brain with resulting neuropathies. Wide local excision with adjuvant radiotherapy where indicated remains the current practice for treatment with chemotherapy predominately being reserved as a salvage treatment for patients with disseminated disease.
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spelling pubmed-34860092012-11-06 Neurotropic Melanoma: The Management of Localised Disease Croker, Jeremy Burmeister, Bryan Foote, Matthew J Skin Cancer Review Article Neurotropic melanoma is a rare subtype of cutaneous malignant melanoma. Compared with conventional melanoma, it is more locally aggressive with an increased tendency for local recurrence but less likely for nodal or distant metastases. These tumours can be a diagnostic dilemma with a variety of morphological, histopathological, and immunophenotypical expressions. The often amelanotic, benign appearance may lead to treatment issues such as late presentation, diagnostic delay, misdiagnosis, insufficient surgical margins, and recurrence with resulting poor outcome. The neurotropic nature of the disease and prevalence in the head and neck region can result in perineural and neural invasion along named large nerves into the brain with resulting neuropathies. Wide local excision with adjuvant radiotherapy where indicated remains the current practice for treatment with chemotherapy predominately being reserved as a salvage treatment for patients with disseminated disease. Hindawi Publishing Corporation 2012 2012-10-22 /pmc/articles/PMC3486009/ /pubmed/23133758 http://dx.doi.org/10.1155/2012/706452 Text en Copyright © 2012 Jeremy Croker et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Croker, Jeremy
Burmeister, Bryan
Foote, Matthew
Neurotropic Melanoma: The Management of Localised Disease
title Neurotropic Melanoma: The Management of Localised Disease
title_full Neurotropic Melanoma: The Management of Localised Disease
title_fullStr Neurotropic Melanoma: The Management of Localised Disease
title_full_unstemmed Neurotropic Melanoma: The Management of Localised Disease
title_short Neurotropic Melanoma: The Management of Localised Disease
title_sort neurotropic melanoma: the management of localised disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3486009/
https://www.ncbi.nlm.nih.gov/pubmed/23133758
http://dx.doi.org/10.1155/2012/706452
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