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Early diagnosis of genital mucosal melanoma: how good are our dermoscopic criteria?

BACKGROUND: There are limited studies on the dermoscopic features of mucosal melanoma, particularly early-stage lesions. Described criteria include the presence of blue, gray, or white colors, with a reported sensitivity of 100%. It is unclear if these features will aid in the detection of early muc...

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Autores principales: Rogers, Tova, Pulitzer, Melissa, Marino, Maria L., Marghoob, Ashfaq A., Zivanovic, Oliver, Marchetti, Michael A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Derm101.com 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108646/
https://www.ncbi.nlm.nih.gov/pubmed/27867747
http://dx.doi.org/10.5826/dpc.0604a10
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author Rogers, Tova
Pulitzer, Melissa
Marino, Maria L.
Marghoob, Ashfaq A.
Zivanovic, Oliver
Marchetti, Michael A.
author_facet Rogers, Tova
Pulitzer, Melissa
Marino, Maria L.
Marghoob, Ashfaq A.
Zivanovic, Oliver
Marchetti, Michael A.
author_sort Rogers, Tova
collection PubMed
description BACKGROUND: There are limited studies on the dermoscopic features of mucosal melanoma, particularly early-stage lesions. Described criteria include the presence of blue, gray, or white colors, with a reported sensitivity of 100%. It is unclear if these features will aid in the detection of early mucosal melanoma or improve diagnostic accuracy compared to naked-eye examination alone. CASE: An Asian female in her fifties was referred for evaluation of an asymptomatic, irregularly pigmented patch of the clitoral hood and labia minora of unknown duration. Her past medical history was notable for Stage IV non-small cell lung cancer. She denied a personal or family history of skin cancer. Dermoscopic evaluation of the vulvar lesion revealed heterogeneous brown and black pigmentation mostly composed of thick lines. There were no other colors or structures present. As the differential diagnosis included vulvar melanosis and mucosal melanoma, the patient was recommended to undergo biopsy, which was delayed due to complications from her underlying lung cancer. Repeat dermoscopic imaging performed three months later revealed significant changes concerning for melanoma, including increase in size, asymmetric darkening, and the appearance of structureless areas and central blue and pink colors. Histopathological examination of a biopsy and subsequent resection confirmed the diagnosis of melanoma in situ. CONCLUSION: Previously described dermoscopic features for mucosal melanoma may not have high sensitivity for early melanomas. Additional studies are needed to define the dermoscopic characteristics of mucosal melanomas that aid in early detection. Health care providers should have a low threshold for biopsy of mucosal lesions that show any clinical or dermoscopic features of melanoma, especially in older women.
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spelling pubmed-51086462016-11-18 Early diagnosis of genital mucosal melanoma: how good are our dermoscopic criteria? Rogers, Tova Pulitzer, Melissa Marino, Maria L. Marghoob, Ashfaq A. Zivanovic, Oliver Marchetti, Michael A. Dermatol Pract Concept Articles BACKGROUND: There are limited studies on the dermoscopic features of mucosal melanoma, particularly early-stage lesions. Described criteria include the presence of blue, gray, or white colors, with a reported sensitivity of 100%. It is unclear if these features will aid in the detection of early mucosal melanoma or improve diagnostic accuracy compared to naked-eye examination alone. CASE: An Asian female in her fifties was referred for evaluation of an asymptomatic, irregularly pigmented patch of the clitoral hood and labia minora of unknown duration. Her past medical history was notable for Stage IV non-small cell lung cancer. She denied a personal or family history of skin cancer. Dermoscopic evaluation of the vulvar lesion revealed heterogeneous brown and black pigmentation mostly composed of thick lines. There were no other colors or structures present. As the differential diagnosis included vulvar melanosis and mucosal melanoma, the patient was recommended to undergo biopsy, which was delayed due to complications from her underlying lung cancer. Repeat dermoscopic imaging performed three months later revealed significant changes concerning for melanoma, including increase in size, asymmetric darkening, and the appearance of structureless areas and central blue and pink colors. Histopathological examination of a biopsy and subsequent resection confirmed the diagnosis of melanoma in situ. CONCLUSION: Previously described dermoscopic features for mucosal melanoma may not have high sensitivity for early melanomas. Additional studies are needed to define the dermoscopic characteristics of mucosal melanomas that aid in early detection. Health care providers should have a low threshold for biopsy of mucosal lesions that show any clinical or dermoscopic features of melanoma, especially in older women. Derm101.com 2016-10-31 /pmc/articles/PMC5108646/ /pubmed/27867747 http://dx.doi.org/10.5826/dpc.0604a10 Text en ©2016 Rogers. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Articles
Rogers, Tova
Pulitzer, Melissa
Marino, Maria L.
Marghoob, Ashfaq A.
Zivanovic, Oliver
Marchetti, Michael A.
Early diagnosis of genital mucosal melanoma: how good are our dermoscopic criteria?
title Early diagnosis of genital mucosal melanoma: how good are our dermoscopic criteria?
title_full Early diagnosis of genital mucosal melanoma: how good are our dermoscopic criteria?
title_fullStr Early diagnosis of genital mucosal melanoma: how good are our dermoscopic criteria?
title_full_unstemmed Early diagnosis of genital mucosal melanoma: how good are our dermoscopic criteria?
title_short Early diagnosis of genital mucosal melanoma: how good are our dermoscopic criteria?
title_sort early diagnosis of genital mucosal melanoma: how good are our dermoscopic criteria?
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108646/
https://www.ncbi.nlm.nih.gov/pubmed/27867747
http://dx.doi.org/10.5826/dpc.0604a10
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