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新生儿短暂性大疱性皮肤松解症。病例报告及发病机制综述。

Transient bullous dermolysis of the newborn. Case report and review of pathogenesis.

作者信息

Eng A M, Keegan C A, Hashimoto K, Rhee H L, Bronson D M, Tenner L K, Goldin H M

机构信息

Department of Dermatology, Cook County Hospital, Chicago, IL 60612-9985.

出版信息

J Cutan Pathol. 1991 Oct;18(5):328-32. doi: 10.1111/j.1600-0560.1991.tb01544.x.

Abstract

A case of transient bullous dermolysis of the newborn is reported. A healthy Hispanic newborn developed bullae during the first two days of life. From age two to four weeks, the lesions healed with milia formation. There was no residual scarring or hypopigmentation. An induced blister showed dermal-epidermal separation with the PAS-positive basement membrane in the epidermal roof. PAS-positive inclusions were present in the cytoplasm of a few basal cells. Examination by electron microscopy showed degeneration of the collagen and anchoring fibrils. There were numerous stellate inclusions in the endoplasmic reticulum of the cytoplasm of the lesional basal keratinocytes.

摘要

报告了一例新生儿短暂性大疱性皮肤松解症。一名健康的西班牙裔新生儿在出生后的前两天出现大疱。从两周到四周龄,皮损愈合并形成粟丘疹。无残留瘢痕或色素减退。诱导性水疱显示真皮-表皮分离,表皮顶部有PAS阳性的基底膜。少数基底细胞的细胞质中有PAS阳性包涵体。电子显微镜检查显示胶原蛋白和锚定原纤维变性。病变基底角质形成细胞细胞质的内质网中有许多星状包涵体。

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