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多孔性汗腺瘤:两例报告及文献综述

Poroid Hidradenoma: A Two-Case Report and Literature Review.

作者信息

Lim Joon Soo, Kwon Eun Sun, Myung Ki Bum, Cheong Seung Hyun

机构信息

Department of Dermatology, Konyang University College of Medicine, Daejeon, Korea.

出版信息

Ann Dermatol. 2021 Jun;33(3):289-292. doi: 10.5021/ad.2021.33.3.289. Epub 2021 May 4.

Abstract

Poroid hidradenoma (PH) is a rare benign tumor that shows differentiation of the eccrine sweat gland. It occurs mainly in adults, presenting as a 0.5 to 2 cm-sized intradermal nodule, mostly on the head, extremities, trunk and neck. We report two rare cases of PH, one on the face and the other on the heel. The first patient was a 50-year-old male who had a solitary, skin-colored nodule on his right temple for 6 months. The second patient was a 67-year-old female who presented with a solitary, bean-sized, tender nodule on her left heel for 1 year. The common histological examination finding was a well-circumscribed tumor composed of solid portions and large cystic spaces in the center. The tumor cells consisted of small, monomorphic poroid cells and large cuticular cells in both cases. To our knowledge, only few cases of PH have been reported. Herein, we report two rare cases of PHs with literature review.

摘要

多孔性汗腺瘤(PH)是一种罕见的良性肿瘤,表现为小汗腺分化。它主要发生于成年人,表现为直径0.5至2厘米的皮内结节,多见于头部、四肢、躯干和颈部。我们报告两例罕见的多孔性汗腺瘤病例,一例位于面部,另一例位于足跟。首例患者为一名50岁男性,其右颞部有一个孤立的肤色结节,已存在6个月。第二例患者是一名67岁女性,其左脚跟有一个孤立的豆状压痛结节,已存在1年。常见的组织学检查结果是一个边界清楚的肿瘤,由实性部分和中央大囊腔组成。两例肿瘤细胞均由小的、形态单一的多孔状细胞和大的角质形成细胞构成。据我们所知,仅有少数多孔性汗腺瘤病例被报道。在此,我们报告两例罕见的多孔性汗腺瘤病例并进行文献复习。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5877/8137338/f1b8ab6fb9cb/ad-33-289-g001.jpg

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