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[通过胎儿皮肤活检进行致死性交界性大疱性表皮松解症的产前诊断]

[Prenatal diagnosis of lethal junctional epidermolysis bullosa by fetal skin biopsy].

作者信息

Shimizu H, Schofield O M, Eady R A

机构信息

Department of Cell Pathology, St Thomas's Hospital.

出版信息

Nihon Hifuka Gakkai Zasshi. 1991 Apr;101(5):539-45.

PMID:1890750
Abstract

A 22-year-old woman, whose first infant had died of lethal junctional epidermolysis bullosa (JEB), requested prenatal diagnosis for her third pregnancy. At 20 weeks gestation, fetal biopsy was performed under direct vision by fetoscopy. A semithin section of epon-embedded skin showed dermo-epidermal separation at the light microscopic level. Electron microscopy revealed the site of separation to be within the lamina lucida of the epidermal basement membrane (EBM). Indirect immunofluorescence on a 5 microns cryostat specimen of skin showed a complete absence of GB3 monoclonal antibody immunostaining at the EBM compared with a control 18 week old normal fetal skin sample. The diagnosis was therefore made that the fetus was affected with lethal JEB and a prostaglandin termination performed. The diagnosis was confirmed by further studies on the aborted fetus. 54 cases of prenatal diagnosis of various types of epidermolysis bullosa performed at Institute of Dermatology over the last 10 years are briefly reviewed. Several social and practical problems to launch prenatal diagnosis in Japan are also discussed.

摘要

一名22岁女性,其首个婴儿死于致死性交界性大疱性表皮松解症(JEB),此次第三次怀孕时要求进行产前诊断。妊娠20周时,通过胎儿镜在直视下进行了胎儿活检。环氧树脂包埋皮肤的半薄切片在光学显微镜下显示真皮-表皮分离。电子显微镜显示分离部位位于表皮基底膜(EBM)的透明层内。对5微米皮肤冰冻切片进行间接免疫荧光检测,结果显示与对照的18周龄正常胎儿皮肤样本相比,EBM处完全没有GB3单克隆抗体免疫染色。因此诊断胎儿患有致死性JEB,并进行了前列腺素引产。对流产胎儿的进一步研究证实了该诊断。本文简要回顾了过去10年在皮肤病研究所进行的54例各种类型大疱性表皮松解症的产前诊断情况。还讨论了在日本开展产前诊断的一些社会和实际问题。

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