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Primary Cutaneous Plasmacytosis: Masquerading as Hidradenitis Suppurativa

Isolated cutaneous plasmacytosis (CP) is a rare entity with few cases reported in world literature. CP masquerading as hidradenitis suppurativa like presentation is a unique case with some features differentiating it clinically from it which were further confirmed by histopathology and immunostainin...

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Detalles Bibliográficos
Autores principales: Goyal, Tarang, Varshney, Anupam, Zawar, Vijay, Sharma, Veena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817452/
https://www.ncbi.nlm.nih.gov/pubmed/27057027
http://dx.doi.org/10.4103/0019-5154.177768
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author Goyal, Tarang
Varshney, Anupam
Zawar, Vijay
Sharma, Veena
author_facet Goyal, Tarang
Varshney, Anupam
Zawar, Vijay
Sharma, Veena
author_sort Goyal, Tarang
collection PubMed
description Isolated cutaneous plasmacytosis (CP) is a rare entity with few cases reported in world literature. CP masquerading as hidradenitis suppurativa like presentation is a unique case with some features differentiating it clinically from it which were further confirmed by histopathology and immunostaining. Our case showed hyperplasia of mature plasma cells and polyclonal hypergammaglobulinemia, immunostaining for CD138 positivity and kappa: lambda ratio more than 3:1. Extensive clinical and laboratory investigations failed to reveal any underlying pathology, presence of any underlying disease accompanying the hypergammaglobulinemia and/or plasma cell proliferation.
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spelling pubmed-48174522016-04-07 Primary Cutaneous Plasmacytosis: Masquerading as Hidradenitis Suppurativa Goyal, Tarang Varshney, Anupam Zawar, Vijay Sharma, Veena Indian J Dermatol Case Report Isolated cutaneous plasmacytosis (CP) is a rare entity with few cases reported in world literature. CP masquerading as hidradenitis suppurativa like presentation is a unique case with some features differentiating it clinically from it which were further confirmed by histopathology and immunostaining. Our case showed hyperplasia of mature plasma cells and polyclonal hypergammaglobulinemia, immunostaining for CD138 positivity and kappa: lambda ratio more than 3:1. Extensive clinical and laboratory investigations failed to reveal any underlying pathology, presence of any underlying disease accompanying the hypergammaglobulinemia and/or plasma cell proliferation. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4817452/ /pubmed/27057027 http://dx.doi.org/10.4103/0019-5154.177768 Text en Copyright: © 2016 Indian Journal of Dermatology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Goyal, Tarang
Varshney, Anupam
Zawar, Vijay
Sharma, Veena
Primary Cutaneous Plasmacytosis: Masquerading as Hidradenitis Suppurativa
title Primary Cutaneous Plasmacytosis: Masquerading as Hidradenitis Suppurativa
title_full Primary Cutaneous Plasmacytosis: Masquerading as Hidradenitis Suppurativa
title_fullStr Primary Cutaneous Plasmacytosis: Masquerading as Hidradenitis Suppurativa
title_full_unstemmed Primary Cutaneous Plasmacytosis: Masquerading as Hidradenitis Suppurativa
title_short Primary Cutaneous Plasmacytosis: Masquerading as Hidradenitis Suppurativa
title_sort primary cutaneous plasmacytosis: masquerading as hidradenitis suppurativa
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817452/
https://www.ncbi.nlm.nih.gov/pubmed/27057027
http://dx.doi.org/10.4103/0019-5154.177768
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