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胎儿盘状肾:产前诊断与产后随访

Fetal Pancake Kidney: Prenatal Diagnosis and Postnatal Follow-up.

作者信息

Perlman Sharon, Borovitz Yael, Bar-Adon Sonya, Dekel Benjamin, Achiron Reuven, Gilboa Yinon

机构信息

Ultrasound Unit, Helen Schneider Women's Hospital, Rabin Medical Center, Petach Tikva, Israel.

Tel-Aviv University, Sackler School of Medicine, Tel-Aviv, Israel.

出版信息

J Ultrasound Med. 2020 Aug;39(8):1665-1668. doi: 10.1002/jum.15251. Epub 2020 Feb 27.

Abstract

Bilateral failure of the kidneys to ascend during embryonic life may lead to fusion of the two renal masses, resulting in a round mass known as pancake kidney. Reviewing the literature, we did not encounter any reports of prenatal diagnosis of pancake kidneys. We present 6 cases of a pancake kidney diagnosed prenatally. Extrarenal associated anomalies included an aberrant right subclavian artery, nonvisualization of the uterus, consistent with Mayer-Rokitansky-Küster-Hauser syndrome, and a sequence of early-onset growth restriction, hypospadias, and syndactyly, suspected as Smith-Lemli-Opitz syndrome. On postnatal follow-up, all infants had a normal renal outcome.

摘要

双侧肾脏在胚胎期未能上升可能导致两个肾块融合,形成一个圆形肿块,即所谓的饼状肾。查阅文献时,我们未发现任何关于饼状肾产前诊断的报告。我们报告6例产前诊断为饼状肾的病例。肾外相关异常包括右锁骨下动脉异常、子宫未显影(符合迈耶-罗基坦斯基-库斯特-豪泽综合征)以及一系列早发性生长受限、尿道下裂和并指(怀疑为史密斯-勒米-奥皮茨综合征)。产后随访显示,所有婴儿的肾脏结局均正常。

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