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Balloon cell melanoma: a case report with polarized and non-polarized dermatoscopy and dermatopathology

Balloon cell melanoma is a rare melanoma subtype, with only one previous case with dermatoscopy published. It is often non-pigmented, leading to diagnostic difficulty, and there is a tendency for lesions to be thick at diagnosis. We report a case of balloon cell melanoma on the forearm of a 61-year-...

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Autores principales: Maher, James, Cameron, Alan, Wallace, Sharon, Acosta-Rojas, Rafael, Weedon, David, Rosendahl, Cliff
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Derm101.com 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3919844/
https://www.ncbi.nlm.nih.gov/pubmed/24520518
http://dx.doi.org/10.5826/dpc.0401a11
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author Maher, James
Cameron, Alan
Wallace, Sharon
Acosta-Rojas, Rafael
Weedon, David
Rosendahl, Cliff
author_facet Maher, James
Cameron, Alan
Wallace, Sharon
Acosta-Rojas, Rafael
Weedon, David
Rosendahl, Cliff
author_sort Maher, James
collection PubMed
description Balloon cell melanoma is a rare melanoma subtype, with only one previous case with dermatoscopy published. It is often non-pigmented, leading to diagnostic difficulty, and there is a tendency for lesions to be thick at diagnosis. We report a case of balloon cell melanoma on the forearm of a 61-year-old man with both polarized and non-polarized dermatoscopy and dermatopathology. It presented as a firm pale nodule with focal eccentric pigmentation. The clinical images evoke a differential diagnosis of dermatofibroma, dermal nevus, Spitz nevus and basal cell carcinoma as well as melanoma. This melanoma was partially pigmented due to a small, pigmented superficial spreading component on the edge of the non-pigmented balloon cell nodule, prompting further evaluation. In retrospect there was the clue to malignancy of polarizing-specific white lines (chrysalis structures) and polymorphous vessels, including a pattern of dot vessels. The reticular lines exclude basal cell carcinoma, polarizing-specific white lines are inconsistent with the diagnosis of dermal nevus and their eccentric location is inconsistent with both Spitz nevus and dermatofibroma. Excision biopsy was performed, revealing a superficial spreading melanoma with two distinct invasive components, one of atypical non-mature epithelioid cells and the other an amelanotic nodular component, comprising more than 50% of the lesion, characterized by markedly distended epithelioid melanocytes showing pseudo-xanthomatous cytoplasmic balloon cell morphology. A diagnosis of balloon cell melanoma, Breslow thickness 1.9 mm, mitotic rate 3 per square millimeter was rendered. Wide local excision was performed, as was sentinel lymph node biopsy, which was negative.
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spelling pubmed-39198442014-02-11 Balloon cell melanoma: a case report with polarized and non-polarized dermatoscopy and dermatopathology Maher, James Cameron, Alan Wallace, Sharon Acosta-Rojas, Rafael Weedon, David Rosendahl, Cliff Dermatol Pract Concept Observation Balloon cell melanoma is a rare melanoma subtype, with only one previous case with dermatoscopy published. It is often non-pigmented, leading to diagnostic difficulty, and there is a tendency for lesions to be thick at diagnosis. We report a case of balloon cell melanoma on the forearm of a 61-year-old man with both polarized and non-polarized dermatoscopy and dermatopathology. It presented as a firm pale nodule with focal eccentric pigmentation. The clinical images evoke a differential diagnosis of dermatofibroma, dermal nevus, Spitz nevus and basal cell carcinoma as well as melanoma. This melanoma was partially pigmented due to a small, pigmented superficial spreading component on the edge of the non-pigmented balloon cell nodule, prompting further evaluation. In retrospect there was the clue to malignancy of polarizing-specific white lines (chrysalis structures) and polymorphous vessels, including a pattern of dot vessels. The reticular lines exclude basal cell carcinoma, polarizing-specific white lines are inconsistent with the diagnosis of dermal nevus and their eccentric location is inconsistent with both Spitz nevus and dermatofibroma. Excision biopsy was performed, revealing a superficial spreading melanoma with two distinct invasive components, one of atypical non-mature epithelioid cells and the other an amelanotic nodular component, comprising more than 50% of the lesion, characterized by markedly distended epithelioid melanocytes showing pseudo-xanthomatous cytoplasmic balloon cell morphology. A diagnosis of balloon cell melanoma, Breslow thickness 1.9 mm, mitotic rate 3 per square millimeter was rendered. Wide local excision was performed, as was sentinel lymph node biopsy, which was negative. Derm101.com 2014-01-31 /pmc/articles/PMC3919844/ /pubmed/24520518 http://dx.doi.org/10.5826/dpc.0401a11 Text en Copyright: ©2014 Maher et al. 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 Observation
Maher, James
Cameron, Alan
Wallace, Sharon
Acosta-Rojas, Rafael
Weedon, David
Rosendahl, Cliff
Balloon cell melanoma: a case report with polarized and non-polarized dermatoscopy and dermatopathology
title Balloon cell melanoma: a case report with polarized and non-polarized dermatoscopy and dermatopathology
title_full Balloon cell melanoma: a case report with polarized and non-polarized dermatoscopy and dermatopathology
title_fullStr Balloon cell melanoma: a case report with polarized and non-polarized dermatoscopy and dermatopathology
title_full_unstemmed Balloon cell melanoma: a case report with polarized and non-polarized dermatoscopy and dermatopathology
title_short Balloon cell melanoma: a case report with polarized and non-polarized dermatoscopy and dermatopathology
title_sort balloon cell melanoma: a case report with polarized and non-polarized dermatoscopy and dermatopathology
topic Observation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3919844/
https://www.ncbi.nlm.nih.gov/pubmed/24520518
http://dx.doi.org/10.5826/dpc.0401a11
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