Porokeratosis of the scrotum: a case report and literature review
Porokeratosis, a keratinizing disorder of unknown etiology, exhibits an autosomal dominant inheritance pattern or manifests as an isolated acquired dermatosis. This condition can occur at any site on the skin; however, scrotal lesions are extremely rare. Only 18 cases of scrotal lesions were identif...
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Format: | Article |
Language: | English |
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Frontiers Media S.A.
2024-01-01
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Series: | Frontiers in Medicine |
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Online Access: | https://www.frontiersin.org/articles/10.3389/fmed.2023.1274635/full |
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author | Xiaorong Zhang Bangtao Chen Jing Yang |
author_facet | Xiaorong Zhang Bangtao Chen Jing Yang |
author_sort | Xiaorong Zhang |
collection | DOAJ |
description | Porokeratosis, a keratinizing disorder of unknown etiology, exhibits an autosomal dominant inheritance pattern or manifests as an isolated acquired dermatosis. This condition can occur at any site on the skin; however, scrotal lesions are extremely rare. Only 18 cases of scrotal lesions were identified through a comprehensive review of the relevant literature. Herein, we present a case of a 19-year-old patient with porokeratosis of the scrotum. Additionally, we provide a summary of the etiologies, clinical manifestations, and histopathology of scrotal porokeratosis, and present differential diagnoses by reviewing the related literature. |
first_indexed | 2024-03-08T16:06:57Z |
format | Article |
id | doaj.art-f2fe676e4b614441a55cf5c718e7e3d8 |
institution | Directory Open Access Journal |
issn | 2296-858X |
language | English |
last_indexed | 2024-03-08T16:06:57Z |
publishDate | 2024-01-01 |
publisher | Frontiers Media S.A. |
record_format | Article |
series | Frontiers in Medicine |
spelling | doaj.art-f2fe676e4b614441a55cf5c718e7e3d82024-01-08T05:54:37ZengFrontiers Media S.A.Frontiers in Medicine2296-858X2024-01-011010.3389/fmed.2023.12746351274635Porokeratosis of the scrotum: a case report and literature reviewXiaorong ZhangBangtao ChenJing YangPorokeratosis, a keratinizing disorder of unknown etiology, exhibits an autosomal dominant inheritance pattern or manifests as an isolated acquired dermatosis. This condition can occur at any site on the skin; however, scrotal lesions are extremely rare. Only 18 cases of scrotal lesions were identified through a comprehensive review of the relevant literature. Herein, we present a case of a 19-year-old patient with porokeratosis of the scrotum. Additionally, we provide a summary of the etiologies, clinical manifestations, and histopathology of scrotal porokeratosis, and present differential diagnoses by reviewing the related literature.https://www.frontiersin.org/articles/10.3389/fmed.2023.1274635/fullscrotal porokeratosisrarehistopathologyclinical manifestationsdiagnosis |
spellingShingle | Xiaorong Zhang Bangtao Chen Jing Yang Porokeratosis of the scrotum: a case report and literature review Frontiers in Medicine scrotal porokeratosis rare histopathology clinical manifestations diagnosis |
title | Porokeratosis of the scrotum: a case report and literature review |
title_full | Porokeratosis of the scrotum: a case report and literature review |
title_fullStr | Porokeratosis of the scrotum: a case report and literature review |
title_full_unstemmed | Porokeratosis of the scrotum: a case report and literature review |
title_short | Porokeratosis of the scrotum: a case report and literature review |
title_sort | porokeratosis of the scrotum a case report and literature review |
topic | scrotal porokeratosis rare histopathology clinical manifestations diagnosis |
url | https://www.frontiersin.org/articles/10.3389/fmed.2023.1274635/full |
work_keys_str_mv | AT xiaorongzhang porokeratosisofthescrotumacasereportandliteraturereview AT bangtaochen porokeratosisofthescrotumacasereportandliteraturereview AT jingyang porokeratosisofthescrotumacasereportandliteraturereview |