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重新审视戈尔茨综合征的组织病理学发现。

Revisiting histopathologic findings in Goltz syndrome.

作者信息

Ko Christine J, Antaya Richard J, Zubek Amanda, Craiglow Brittany, Damsky William, Galan Anjela, McNiff Jennifer M

机构信息

Department of Dermatology, Yale University, New Haven, CT, USA.

Department of Pathology, Yale University, New Haven, CT, USA.

出版信息

J Cutan Pathol. 2016 May;43(5):418-21. doi: 10.1111/cup.12699. Epub 2016 Apr 5.

Abstract

Goltz syndrome (focal dermal hypoplasia) is an X-linked dominant disorder that is classically associated with yellowish papules representing fat herniation (superficial adipocytes). We report a series of three cases, with clinicopathologic correlation of biopsies from Blaschkoid streaks. A range of histopathologic features, including some underreported findings (increased papillary dermal blood vessels, decreased thickness of the dermis, and adipocytes high in the dermis), are reproducible and can strongly point to the correct diagnosis of Goltz syndrome.

摘要

戈尔茨综合征(局灶性真皮发育不全)是一种X连锁显性疾病,典型表现为代表脂肪疝出(浅表脂肪细胞)的淡黄色丘疹。我们报告了三例病例,并对Blaschkoid条纹处活检组织进行了临床病理相关性分析。一系列组织病理学特征,包括一些此前报道较少的发现(乳头真皮层血管增多、真皮厚度变薄以及真皮浅层脂肪细胞),具有可重复性,能够有力地指向戈尔茨综合征的正确诊断。

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