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Apocrine Hidrocystoma with IgG4 Plasma Cell Infiltration Presenting as Recurrent Chalazion: A Case Report

Apocrine hidrocystomas are benign cystic tumors resulting from apocrine sweat glands’ proliferation. They typically present as solitary, slow-growing nodules at the head and neck, especially in the periorbital cutaneous region. We present a case of periorbital apocrine hidrocystoma in a 22-year-old...

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Autores principales: Wu, Shang-Yen, Huang, Jin-Wei, Lee, Yuan-Chieh, Chang, Fang-Ling, Li, Ming-Hsun, Chen, Nancy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9317353/
https://www.ncbi.nlm.nih.gov/pubmed/35888558
http://dx.doi.org/10.3390/medicina58070840
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author Wu, Shang-Yen
Huang, Jin-Wei
Lee, Yuan-Chieh
Chang, Fang-Ling
Li, Ming-Hsun
Chen, Nancy
author_facet Wu, Shang-Yen
Huang, Jin-Wei
Lee, Yuan-Chieh
Chang, Fang-Ling
Li, Ming-Hsun
Chen, Nancy
author_sort Wu, Shang-Yen
collection PubMed
description Apocrine hidrocystomas are benign cystic tumors resulting from apocrine sweat glands’ proliferation. They typically present as solitary, slow-growing nodules at the head and neck, especially in the periorbital cutaneous region. We present a case of periorbital apocrine hidrocystoma in a 22-year-old woman that was treated as chalazion previously. Besides the hallmark histopathological findings of apocrine hidrocystoma, IgG4 plasma cell infiltration of the cystic wall was also found. The ratio of IgG4-to-IgG-positive plasma cells was high, whereas serum IgG4 was within the standard limit. This is, to date, the only probable IgG4-related ophthalmic disease associated with apocrine hidrocystoma.
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spelling pubmed-93173532022-07-27 Apocrine Hidrocystoma with IgG4 Plasma Cell Infiltration Presenting as Recurrent Chalazion: A Case Report Wu, Shang-Yen Huang, Jin-Wei Lee, Yuan-Chieh Chang, Fang-Ling Li, Ming-Hsun Chen, Nancy Medicina (Kaunas) Case Report Apocrine hidrocystomas are benign cystic tumors resulting from apocrine sweat glands’ proliferation. They typically present as solitary, slow-growing nodules at the head and neck, especially in the periorbital cutaneous region. We present a case of periorbital apocrine hidrocystoma in a 22-year-old woman that was treated as chalazion previously. Besides the hallmark histopathological findings of apocrine hidrocystoma, IgG4 plasma cell infiltration of the cystic wall was also found. The ratio of IgG4-to-IgG-positive plasma cells was high, whereas serum IgG4 was within the standard limit. This is, to date, the only probable IgG4-related ophthalmic disease associated with apocrine hidrocystoma. MDPI 2022-06-22 /pmc/articles/PMC9317353/ /pubmed/35888558 http://dx.doi.org/10.3390/medicina58070840 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Wu, Shang-Yen
Huang, Jin-Wei
Lee, Yuan-Chieh
Chang, Fang-Ling
Li, Ming-Hsun
Chen, Nancy
Apocrine Hidrocystoma with IgG4 Plasma Cell Infiltration Presenting as Recurrent Chalazion: A Case Report
title Apocrine Hidrocystoma with IgG4 Plasma Cell Infiltration Presenting as Recurrent Chalazion: A Case Report
title_full Apocrine Hidrocystoma with IgG4 Plasma Cell Infiltration Presenting as Recurrent Chalazion: A Case Report
title_fullStr Apocrine Hidrocystoma with IgG4 Plasma Cell Infiltration Presenting as Recurrent Chalazion: A Case Report
title_full_unstemmed Apocrine Hidrocystoma with IgG4 Plasma Cell Infiltration Presenting as Recurrent Chalazion: A Case Report
title_short Apocrine Hidrocystoma with IgG4 Plasma Cell Infiltration Presenting as Recurrent Chalazion: A Case Report
title_sort apocrine hidrocystoma with igg4 plasma cell infiltration presenting as recurrent chalazion: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9317353/
https://www.ncbi.nlm.nih.gov/pubmed/35888558
http://dx.doi.org/10.3390/medicina58070840
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