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汗腺顶泌性棘层松解性疾病。格罗弗病的一个亚型。

Sudoriferous acrosyringeal acantholytic disease. A subset of Grover's disease.

作者信息

Hashimoto K, Moiin A, Chang M W, Tada J

机构信息

Department of Dermatology & Syphilology, Wayne State University School of Medicine, Detroit, Michigan, USA.

出版信息

J Cutan Pathol. 1996 Apr;23(2):151-64. doi: 10.1111/j.1600-0560.1996.tb01289.x.

Abstract

Three selected cases of transient acantholytic dermatosis were studied because of their definitive correlation with sweating due to fever and/ or bed-ridden situations. Biopsy specimens were serially sectioned and acantholysis was found in the acrosyringium or traced to connect to the acrosyringium in all biopsy specimens. Carcinoembryonic antigen (CEA) and eccrine gland-specific monoclonal antibody, IKH-4, were positive in acantholytic cells. Electron microscopy revealed electron dense material filling the lumen of intraepidermal eccrine ducts. This material leaked into lateral intercellular spaces of the luminal cells, passing tight junctions. Marked edema and numerous lysosomes were reminiscent of those found when eccrine acrosyringium is formed in the embryo; this suggested that an occluded and damaged eccrine intraepidermal duct was being rebuilt via lysosomal digestion.

摘要

选取了三例暂时性棘层松解性皮病病例进行研究,因为它们与发热和/或卧床情况导致的出汗有明确关联。对活检标本进行连续切片,发现所有活检标本中在汗腺导管末端存在棘层松解,或追踪发现其与汗腺导管末端相连。癌胚抗原(CEA)和汗腺特异性单克隆抗体IKH - 4在棘层松解细胞中呈阳性。电子显微镜检查显示电子致密物质填充表皮内汗腺导管的管腔。这种物质通过紧密连接泄漏到管腔细胞的侧向细胞间隙中。明显的水肿和大量溶酶体让人联想到胚胎期形成汗腺导管末端时的情况;这表明表皮内闭塞且受损的汗腺导管正在通过溶酶体消化进行重建。

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