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Steatocystoma Multiplex Confined to the Scalp with Concurrent Alopecia

Steatocystoma multiplex (SM) is an uncommon disorder of the pilosebaceous unit characterized by the development of numerous sebum-containing dermal cysts which rarely involves the scalp. Here, we report a case of a 50-year-old man with multiple cystic nodules and alopecic patches on his scalp. On hi...

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Autores principales: Lee, Deborah, Chun, Ji-Sung, Hong, Soon-Kwon, Seo, Jong-Keun, Choi, Joon-Hee, Koh, Jae-Kyoung, Sung, Ho-Suk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Dermatological Association; The Korean Society for Investigative Dermatology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3229080/
https://www.ncbi.nlm.nih.gov/pubmed/22148065
http://dx.doi.org/10.5021/ad.2011.23.S2.S258
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author Lee, Deborah
Chun, Ji-Sung
Hong, Soon-Kwon
Seo, Jong-Keun
Choi, Joon-Hee
Koh, Jae-Kyoung
Sung, Ho-Suk
author_facet Lee, Deborah
Chun, Ji-Sung
Hong, Soon-Kwon
Seo, Jong-Keun
Choi, Joon-Hee
Koh, Jae-Kyoung
Sung, Ho-Suk
author_sort Lee, Deborah
collection PubMed
description Steatocystoma multiplex (SM) is an uncommon disorder of the pilosebaceous unit characterized by the development of numerous sebum-containing dermal cysts which rarely involves the scalp. Here, we report a case of a 50-year-old man with multiple cystic nodules and alopecic patches on his scalp. On histopathological examination, the folded cyst was found to be lined by stratified squamous epithelium, while flattened sebaceous gland cells were identified in the cystic wall. Pigment casts were present in the hair papillae and perifollicular regions, suggesting trichotillomania as a possible cause of the observed alopecia. This case appears to represent an unusual clinical manifestation of SM.
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spelling pubmed-32290802011-12-06 Steatocystoma Multiplex Confined to the Scalp with Concurrent Alopecia Lee, Deborah Chun, Ji-Sung Hong, Soon-Kwon Seo, Jong-Keun Choi, Joon-Hee Koh, Jae-Kyoung Sung, Ho-Suk Ann Dermatol Case Report Steatocystoma multiplex (SM) is an uncommon disorder of the pilosebaceous unit characterized by the development of numerous sebum-containing dermal cysts which rarely involves the scalp. Here, we report a case of a 50-year-old man with multiple cystic nodules and alopecic patches on his scalp. On histopathological examination, the folded cyst was found to be lined by stratified squamous epithelium, while flattened sebaceous gland cells were identified in the cystic wall. Pigment casts were present in the hair papillae and perifollicular regions, suggesting trichotillomania as a possible cause of the observed alopecia. This case appears to represent an unusual clinical manifestation of SM. Korean Dermatological Association; The Korean Society for Investigative Dermatology 2011-10 2011-10-31 /pmc/articles/PMC3229080/ /pubmed/22148065 http://dx.doi.org/10.5021/ad.2011.23.S2.S258 Text en Copyright © 2011 Korean Dermatological Association; The Korean Society for Investigative Dermatology http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Lee, Deborah
Chun, Ji-Sung
Hong, Soon-Kwon
Seo, Jong-Keun
Choi, Joon-Hee
Koh, Jae-Kyoung
Sung, Ho-Suk
Steatocystoma Multiplex Confined to the Scalp with Concurrent Alopecia
title Steatocystoma Multiplex Confined to the Scalp with Concurrent Alopecia
title_full Steatocystoma Multiplex Confined to the Scalp with Concurrent Alopecia
title_fullStr Steatocystoma Multiplex Confined to the Scalp with Concurrent Alopecia
title_full_unstemmed Steatocystoma Multiplex Confined to the Scalp with Concurrent Alopecia
title_short Steatocystoma Multiplex Confined to the Scalp with Concurrent Alopecia
title_sort steatocystoma multiplex confined to the scalp with concurrent alopecia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3229080/
https://www.ncbi.nlm.nih.gov/pubmed/22148065
http://dx.doi.org/10.5021/ad.2011.23.S2.S258
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