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单纯性大疱性表皮松解症(克布纳型)是一种角蛋白紊乱疾病。超微结构和免疫组织化学研究。

Epidermolysis bullosa simplex (Koebner) is a keratin disorder. Ultrastructural and immunohistochemical study.

作者信息

Ito M, Okuda C, Shimizu N, Tazawa T, Sato Y

机构信息

Department of Dermatology, Niigata (Japan) University School of Medicine.

出版信息

Arch Dermatol. 1991 Mar;127(3):367-72.

PMID:1705413
Abstract

A skin biopsy specimen was obtained from a 1-month-old female with epidermolysis bullosa simplex (Koebner). Histologically, an intraepidermal separation was seen and considered to be formed by cytolysis of the epidermal basal cells. Ultrastructurally, the basal cells were lacking in cytoplasmic tonofilaments, and the initial change of the cytolysis seemed to be cleavages of the cytoplasm. Immunohistochemically, a basal cell keratin was expressed in a suprabasal cell layer but not in the basal cell layer, and a panepithelial keratin was not detected in the basal cell layer. These findings suggest that keratin production of the epidermal cells may be delayed, resulting in a weakness of the basal cells against minor trauma to the skin.

摘要

从一名患有单纯性大疱性表皮松解症(科布纳型)的1个月大女性身上获取了皮肤活检标本。组织学上,可见表皮内分离,认为是由表皮基底细胞的细胞溶解形成的。超微结构上,基底细胞缺乏细胞质张力丝,细胞溶解的初始变化似乎是细胞质的裂解。免疫组织化学显示,基底细胞角蛋白在上基底细胞层表达,但不在基底细胞层表达,且在基底细胞层未检测到全上皮角蛋白。这些发现表明,表皮细胞的角蛋白产生可能延迟,导致基底细胞对皮肤轻微创伤的抵抗力减弱。

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