Poikiloderma vasculare atrophicans: A distinct clinical entity?

This paper describes a typical case of poikiloderma vasculare atrophicans (PVA) in a 48-year-old female. Histologically, the features were suggestive of PVA with the absence of Pautrier′s microabscess or atypical lymphoid cells. The biopsy specimen was positive for cluster of differentiation (CD) 8...

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Main Authors: Vikram K Mahajan, Pushpinder S Chauhan, Karaninder S Mehta, Anju Lath Sharma
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2015-01-01
Series:Indian Journal of Dermatology
Subjects:
Online Access:http://www.e-ijd.org/article.asp?issn=0019-5154;year=2015;volume=60;issue=2;spage=216;epage=216;aulast=Mahajan
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author Vikram K Mahajan
Pushpinder S Chauhan
Karaninder S Mehta
Anju Lath Sharma
author_facet Vikram K Mahajan
Pushpinder S Chauhan
Karaninder S Mehta
Anju Lath Sharma
author_sort Vikram K Mahajan
collection DOAJ
description This paper describes a typical case of poikiloderma vasculare atrophicans (PVA) in a 48-year-old female. Histologically, the features were suggestive of PVA with the absence of Pautrier′s microabscess or atypical lymphoid cells. The biopsy specimen was positive for cluster of differentiation (CD) 8 on immunohistochemical staining. Its exact pathogenesis remains obscure, and it remains unclear whether PVA actually is mycosis fungoides (MF), a forme fruste of MF, or a distinct and benign dermatosis with CD8+ phenotype that can perhaps be labeled as PVA. However, it has a long benign clinical course without progression to tumor stage of MF in most cases, and its status within the spectrum of cutaneous T-cell lymphoma remains poorly understood. Yet it is imperative to distinguish PVA from poikilodermic MF.
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spelling doaj.art-3ec77cc6273c453f83e52c05cd0bd5662022-12-21T23:47:36ZengWolters Kluwer Medknow PublicationsIndian Journal of Dermatology0019-51541998-36112015-01-0160221621610.4103/0019-5154.152566Poikiloderma vasculare atrophicans: A distinct clinical entity?Vikram K MahajanPushpinder S ChauhanKaraninder S MehtaAnju Lath SharmaThis paper describes a typical case of poikiloderma vasculare atrophicans (PVA) in a 48-year-old female. Histologically, the features were suggestive of PVA with the absence of Pautrier′s microabscess or atypical lymphoid cells. The biopsy specimen was positive for cluster of differentiation (CD) 8 on immunohistochemical staining. Its exact pathogenesis remains obscure, and it remains unclear whether PVA actually is mycosis fungoides (MF), a forme fruste of MF, or a distinct and benign dermatosis with CD8+ phenotype that can perhaps be labeled as PVA. However, it has a long benign clinical course without progression to tumor stage of MF in most cases, and its status within the spectrum of cutaneous T-cell lymphoma remains poorly understood. Yet it is imperative to distinguish PVA from poikilodermic MF.http://www.e-ijd.org/article.asp?issn=0019-5154;year=2015;volume=60;issue=2;spage=216;epage=216;aulast=MahajanCollagen vascular disordersparapsoriasis poikilodermiquepoikilodermatous genodermatosespoikilodermic mycosis fungoides
spellingShingle Vikram K Mahajan
Pushpinder S Chauhan
Karaninder S Mehta
Anju Lath Sharma
Poikiloderma vasculare atrophicans: A distinct clinical entity?
Indian Journal of Dermatology
Collagen vascular disorders
parapsoriasis poikilodermique
poikilodermatous genodermatoses
poikilodermic mycosis fungoides
title Poikiloderma vasculare atrophicans: A distinct clinical entity?
title_full Poikiloderma vasculare atrophicans: A distinct clinical entity?
title_fullStr Poikiloderma vasculare atrophicans: A distinct clinical entity?
title_full_unstemmed Poikiloderma vasculare atrophicans: A distinct clinical entity?
title_short Poikiloderma vasculare atrophicans: A distinct clinical entity?
title_sort poikiloderma vasculare atrophicans a distinct clinical entity
topic Collagen vascular disorders
parapsoriasis poikilodermique
poikilodermatous genodermatoses
poikilodermic mycosis fungoides
url http://www.e-ijd.org/article.asp?issn=0019-5154;year=2015;volume=60;issue=2;spage=216;epage=216;aulast=Mahajan
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