Poroid Hidradenoma: Case Report and Comprehensive Review of the Literature.

IF 0.9 Q4 DERMATOLOGY
Case Reports in Dermatology Pub Date : 2023-10-25 eCollection Date: 2023-01-01 DOI:10.1159/000531052
Arrin Brooks, Mariah Morris, Jonathan Cuda, Armein Rahimpour, Semeret Munie
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引用次数: 0

Abstract

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.

息肉样Hidradenoma:病例报告和文献综述。
腺瘤是一种罕见的小汗腺分化的良性附件肿瘤。它是四种描述的多孔性肿瘤变体中最罕见的。PH的特征是具有汗腺癌的结构特征,即肿瘤细胞完全在皮内,同时含有实体和囊性成分,以及主要含有多孔细胞和表皮细胞的多孔肿瘤的细胞学特征。自1990年首次发现PH以来,许多已发表的PH报告称,在文献中可以发现“极少数”PH病例。在这里,我们总共确定了75篇已发表的PH报道,包括这里介绍的病例,以及相关的患者人口统计、病变特征、治疗和结果。我们认为,虽然不常见,但PH可能不是特别罕见,可能是一种少报的诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
57
审稿时长
9 weeks
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