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Poroid Hidradenoma: Case Report and Comprehensive Review of the Literature

Poroid hidradenoma (PH) is a rare benign adnexal tumor of eccrine differentiation. It is the rarest of the four described variants of poroid neoplasms. PHs characteristically share a hybrid of the architectural features of the hidradenoma, namely, tumor cells are entirely intradermal with both solid...

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Autores principales: Brooks, Arrin, Morris, Mariah, Cuda, Jonathan, Rahimpour, Armein, Munie, Semeret
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620550/
https://www.ncbi.nlm.nih.gov/pubmed/37928337
http://dx.doi.org/10.1159/000531052
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author Brooks, Arrin
Morris, Mariah
Cuda, Jonathan
Rahimpour, Armein
Munie, Semeret
author_facet Brooks, Arrin
Morris, Mariah
Cuda, Jonathan
Rahimpour, Armein
Munie, Semeret
author_sort Brooks, Arrin
collection PubMed
description Poroid hidradenoma (PH) is a rare benign adnexal tumor of eccrine differentiation. It is the rarest of the four described variants of poroid neoplasms. PHs characteristically share a hybrid of the architectural features of the hidradenoma, namely, tumor cells are entirely intradermal with both solid and cystic components, and the cytologic characteristics of the poroid neoplasms, containing predominantly poroid and cuticular cells. Many published reports of PH since its original discovery in 1990 state that “very few” cases of PH can be found in the literature. Here, we have identified a total of 75 published accounts of PH, including the case presented here, as well as the associated patient demographics, lesion characteristics, treatment, and outcomes. We suggest that while uncommon, PH is likely not exceptionally rare and could be an underreported diagnosis.
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spelling pubmed-106205502023-11-03 Poroid Hidradenoma: Case Report and Comprehensive Review of the Literature Brooks, Arrin Morris, Mariah Cuda, Jonathan Rahimpour, Armein Munie, Semeret Case Rep Dermatol Case and Review Poroid hidradenoma (PH) is a rare benign adnexal tumor of eccrine differentiation. It is the rarest of the four described variants of poroid neoplasms. PHs characteristically share a hybrid of the architectural features of the hidradenoma, namely, tumor cells are entirely intradermal with both solid and cystic components, and the cytologic characteristics of the poroid neoplasms, containing predominantly poroid and cuticular cells. Many published reports of PH since its original discovery in 1990 state that “very few” cases of PH can be found in the literature. Here, we have identified a total of 75 published accounts of PH, including the case presented here, as well as the associated patient demographics, lesion characteristics, treatment, and outcomes. We suggest that while uncommon, PH is likely not exceptionally rare and could be an underreported diagnosis. S. Karger AG 2023-10-25 /pmc/articles/PMC10620550/ /pubmed/37928337 http://dx.doi.org/10.1159/000531052 Text en © 2023 The Author(s). Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case and Review
Brooks, Arrin
Morris, Mariah
Cuda, Jonathan
Rahimpour, Armein
Munie, Semeret
Poroid Hidradenoma: Case Report and Comprehensive Review of the Literature
title Poroid Hidradenoma: Case Report and Comprehensive Review of the Literature
title_full Poroid Hidradenoma: Case Report and Comprehensive Review of the Literature
title_fullStr Poroid Hidradenoma: Case Report and Comprehensive Review of the Literature
title_full_unstemmed Poroid Hidradenoma: Case Report and Comprehensive Review of the Literature
title_short Poroid Hidradenoma: Case Report and Comprehensive Review of the Literature
title_sort poroid hidradenoma: case report and comprehensive review of the literature
topic Case and Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620550/
https://www.ncbi.nlm.nih.gov/pubmed/37928337
http://dx.doi.org/10.1159/000531052
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