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Key messages from a rare case of annular sarcoidosis of scalp

Sarcoidosis, a multisystem disease of obscure etiology, is characterized by the formation of noncaseating epithelioid cell granulomas in several organs or tissues. The diagnosis of sarcoidosis requires a compatible clinical picture, histologic demonstration of noncaseating granulomas, and exclusion...

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Autores principales: Bhushan, Premanshu, Thatte, Sarvesh S., Singh, Avninder
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/PMC4886594/
https://www.ncbi.nlm.nih.gov/pubmed/27294057
http://dx.doi.org/10.4103/2229-5178.182359
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author Bhushan, Premanshu
Thatte, Sarvesh S.
Singh, Avninder
author_facet Bhushan, Premanshu
Thatte, Sarvesh S.
Singh, Avninder
author_sort Bhushan, Premanshu
collection PubMed
description Sarcoidosis, a multisystem disease of obscure etiology, is characterized by the formation of noncaseating epithelioid cell granulomas in several organs or tissues. The diagnosis of sarcoidosis requires a compatible clinical picture, histologic demonstration of noncaseating granulomas, and exclusion of other diseases capable of producing similar histology or clinical features. The lung is the most commonly affected organ, but the skin is frequently involved. Sarcoidosis occurs worldwide and affects all ages and races with female predominance. Scalp involvement is decidedly rare among the myriad cutaneous manifestations of sarcoidosis. Alopecia is common in sarcoidosis and is generally scarring in nature. Annular sarcoidosis is a rare morphology and annular sarcoid of scalp is seldom reported. Herein we present a case of annular scalp sarcoid with systemic involvement and without alopecia.
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spelling pubmed-48865942016-06-10 Key messages from a rare case of annular sarcoidosis of scalp Bhushan, Premanshu Thatte, Sarvesh S. Singh, Avninder Indian Dermatol Online J Case Report Sarcoidosis, a multisystem disease of obscure etiology, is characterized by the formation of noncaseating epithelioid cell granulomas in several organs or tissues. The diagnosis of sarcoidosis requires a compatible clinical picture, histologic demonstration of noncaseating granulomas, and exclusion of other diseases capable of producing similar histology or clinical features. The lung is the most commonly affected organ, but the skin is frequently involved. Sarcoidosis occurs worldwide and affects all ages and races with female predominance. Scalp involvement is decidedly rare among the myriad cutaneous manifestations of sarcoidosis. Alopecia is common in sarcoidosis and is generally scarring in nature. Annular sarcoidosis is a rare morphology and annular sarcoid of scalp is seldom reported. Herein we present a case of annular scalp sarcoid with systemic involvement and without alopecia. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4886594/ /pubmed/27294057 http://dx.doi.org/10.4103/2229-5178.182359 Text en Copyright: © Indian Dermatology Online Journal 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
Bhushan, Premanshu
Thatte, Sarvesh S.
Singh, Avninder
Key messages from a rare case of annular sarcoidosis of scalp
title Key messages from a rare case of annular sarcoidosis of scalp
title_full Key messages from a rare case of annular sarcoidosis of scalp
title_fullStr Key messages from a rare case of annular sarcoidosis of scalp
title_full_unstemmed Key messages from a rare case of annular sarcoidosis of scalp
title_short Key messages from a rare case of annular sarcoidosis of scalp
title_sort key messages from a rare case of annular sarcoidosis of scalp
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886594/
https://www.ncbi.nlm.nih.gov/pubmed/27294057
http://dx.doi.org/10.4103/2229-5178.182359
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