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引发“汗腺腺瘤样”小汗腺增生的皮肤钙质沉着症:一个极其罕见的病例

Calcinosis Cutis Inducing "Syringomatoid" Eccrine Hyperplasia: An Extremely Rare Example.

作者信息

Hussain Umar A, Ahuero Audrey E, Tschen Jamie A

机构信息

Histopathology, Manchester University NHS Foundation Trust, Manchester, GBR.

Ophthalmology, Ophthalmic Plastic Surgeons of Texas, Houston, USA.

出版信息

Cureus. 2024 Aug 2;16(8):e66016. doi: 10.7759/cureus.66016. eCollection 2024 Aug.

Abstract

Reactive "syringomatoid" eccrine proliferations are a well-established phenomenon, which can show similar but less extensive histological features of a syringoma. The cut-off between syringomatoid hyperplasia and syringomas is subjective and given the considerable morphological overlap, it is possible they represent two points on the same spectrum. Syringomatoid hyperplasia has been associated with several conditions including neoplasms and inflammatory dermatoses. Herein, we describe an extremely rare case of syringomatoid hyperplasia occurring with calcinosis cutis in a 54-year-old Caucasian male. To the best of the authors' knowledge, this is the first such case described in the literature.

摘要

反应性“汗腺腺瘤样”小汗腺增生是一种已被充分认识的现象,其可表现出与汗腺腺瘤相似但范围较小的组织学特征。汗腺腺瘤样增生与汗腺腺瘤之间的界限是主观的,鉴于两者在形态学上有相当大的重叠,它们有可能代表同一谱系上的两个点。汗腺腺瘤样增生与包括肿瘤和炎性皮肤病在内的多种情况相关。在此,我们描述了一例极为罕见的汗腺腺瘤样增生伴皮肤钙质沉着症的病例,患者为一名54岁的白种男性。据作者所知,这是文献中首次报道的此类病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3722/11366260/3e3400edd370/cureus-0016-00000066016-i01.jpg

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