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迟发性汗孔角化性小汗腺孔和真皮导管痣:是否比之前认为的更常见?

Porokeratotic eccrine ostial and dermal duct nevus of late onset: more frequent than previously suggested?

作者信息

Valks R, Abajo P, Fraga J, Aragüés M, García-Diez A

机构信息

Department of Dermatology, Hospital Universitario de la Princesa, Madrid, Spain.

出版信息

Dermatology. 1996;193(2):138-40. doi: 10.1159/000246230.

Abstract

We describe the case of a 10-year-old boy with a porokeratotic eccrine ostial and dermal duct nevus (PEODDN) of late onset. The patient had an 8-year history of multiple keratotic papules on the dorsal surface, and multiple yellowish pitting lesions on the plantar surface of the right foot. Light-microscopic studies of both lesions showed multiple cornoid lamella-like parakeratotic columns, which exclusively arose over eccrine sweat ducts in which the acrosyringium was dilated. Although PEODDN is considered to be a congenital hamartoma of eccrine origin, a review of the literature showed us that the frequency of a late-onset variant may be as high as 26%.

摘要

我们描述了一例10岁迟发性汗孔角化性小汗腺开口和真皮导管痣(PEODDN)男孩的病例。患者背部有多个角化性丘疹病史8年,右脚足底有多个淡黄色凹陷性病变。对这两个病变进行光镜检查显示有多个鸡眼样板层样不全角化柱,这些柱状物仅出现在顶泌汗腺导管扩张的小汗腺导管上。虽然PEODDN被认为是一种先天性小汗腺来源的错构瘤,但文献回顾显示迟发性变异型的发生率可能高达26%。

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