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先天性中胚叶肾瘤的产前诊断:一例预后不良的病例

Prenatal diagnosis of congenital mesoblastic nephroma: a case with poor prognosis.

作者信息

Mata Rodrigo Pereira, Alves Teresa, Figueiredo António, Santos Antónia

机构信息

Gynecology-Obstetrics, Centro Hospitalar Universitário do Algarve, Portimão, Portugal.

Radiology, Hospital Garcia de Orta EPE, Almada, Portugal.

出版信息

BMJ Case Rep. 2019 Aug 28;12(8):e230297. doi: 10.1136/bcr-2019-230297.

Abstract

Congenital mesoblastic nephromais a rare tumour found in neonates, with a very small number of cases diagnosed prenatally. We report a case of a fetal renal tumour suspected at 28 weeks' gestation on routine ultrasound. Prenatal follow-up revealed a severe polyhydramnios at 32 weeks' gestation subsequent amniodrainage was undertaken. She delivered at 34+5 weeks' gestation, after spontaneous premature rupture of membranes.

摘要

先天性中胚层肾瘤是一种在新生儿中发现的罕见肿瘤,产前诊断的病例非常少。我们报告一例在孕28周常规超声检查时疑似胎儿肾肿瘤的病例。产前随访显示孕32周时出现严重羊水过多,随后进行了羊水引流。在胎膜自然早破后,她于孕34 + 5周分娩。

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Regression of a congenital mesoblastic nephroma.先天性中胚层肾瘤的消退。
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[Management of antenatal fetal abdominal tumors. Clues for the diagnosis of a congenital mesoblastic nephroma].
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