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表现为肺动脉狭窄的16三体镶嵌型的产前诊断。

Prenatal diagnosis of trisomy 16 mosaicism manifested as pulmonary artery stenosis.

作者信息

Hidaka Nobuhiro, Yamamoto Nari, Tsukimori Kiyomi, Hojo Satoshi, Suzuki Satoshi O, Wake Norio

机构信息

Department of Obstetrics and Gynecology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashiku, Fukuoka, Japan.

出版信息

J Clin Ultrasound. 2009 Feb;37(2):107-11. doi: 10.1002/jcu.20499.

Abstract

Trisomy 16 mosaicism detected at midtrimester amniocentesis is rare and indicative of true fetal mosaicism. We report a case of mosaic trisomy 16 diagnosed by amniocentesis in which the sonographic findings included fetal pulmonary artery stenosis, a single umbilical artery, and early onset fetal growth restriction. The pregnancy was legally terminated. A review of previous reports suggests that abnormalities of outlet tracts are rarely encountered in fetuses with trisomy 16 mosaicism revealed via amniocentesis.

摘要

孕中期羊膜腔穿刺术检测到的16三体嵌合体很少见,提示真正的胎儿嵌合体。我们报告一例经羊膜腔穿刺术诊断的16三体嵌合体病例,其超声检查结果包括胎儿肺动脉狭窄、单脐动脉和早发性胎儿生长受限。该妊娠依法终止。对既往报告的回顾表明,通过羊膜腔穿刺术发现的16三体嵌合体胎儿很少出现流出道异常。

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