胎儿皮肤活检对致死性大疱性结缔组织松解症的产前诊断。

H Shimizu, O M Schofield, R A Eady
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引用次数: 0

摘要

一名22岁的妇女,她的第一个婴儿死于致命的大疱性结缔组织表皮松解症(JEB),要求对她的第三次怀孕进行产前诊断。在妊娠20周时,通过胎儿镜直视下进行胎儿活检。epon包埋皮肤的半薄切片在光镜下显示真皮-表皮分离。电镜显示分离部位位于表皮基底膜的透明层内。在5微米低温恒温器皮肤样本上的间接免疫荧光显示,与对照组18周龄正常胎儿皮肤样本相比,EBM上完全没有GB3单克隆抗体免疫染色。因此,诊断为胎儿感染了致命的乙脑,并进行了前列腺素终止手术。对流产胎儿的进一步研究证实了这一诊断。本文对近10年来在皮肤科进行的54例不同类型大疱性表皮松解症的产前诊断进行了简要回顾。讨论了在日本开展产前诊断的几个社会和现实问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Prenatal diagnosis of lethal junctional epidermolysis bullosa by fetal skin biopsy].

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.

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