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[孤立性胎儿肾囊肿作为先天性神经母细胞瘤的体征。病例报告及文献综述]

[An isolated fetal kidney cyst as a sign of congenital neuroblastoma. A case report and overview of the literature].

作者信息

Heling K S, Bollmann R, Chaoui R, Tennstedt C, Kirchmair F

机构信息

Abteilung Pränatale Diagnostik und Therapie, Frauenklinik.

出版信息

Geburtshilfe Frauenheilkd. 1995 Jun;55(6):347-50. doi: 10.1055/s-2007-1023331.

Abstract

As a normal scan at 20 weeks of gestation a pregnant woman was referred at 36 weeks because of a cystic tumour in the fetal kidney. The cyst, 27 mm in diameter, was localised at the cranial pole of the right kidney. A fetal neuroblastoma was suspected. At the fourth day after birth adrenalectomy was performed and the histological finding confirmed the prenatal diagnosis. Two years later the child is healthy. In review of the literature we found that sonographic pattern and localisation of fetal neuroblastoma are different, but in all cases the detection was performed in the third trimester of gestation.

摘要

一名孕妇在妊娠20周时进行常规扫描,36周时因胎儿肾内囊性肿瘤前来就诊。囊肿直径27毫米,位于右肾颅极。怀疑是胎儿神经母细胞瘤。出生后第四天进行了肾上腺切除术,组织学检查结果证实了产前诊断。两年后,孩子健康。在文献回顾中我们发现,胎儿神经母细胞瘤的超声图像和定位有所不同,但所有病例均在妊娠晚期进行检测。

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