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先天性中胚叶肾瘤:一例报告

Congenital mesoblastic nephroma: a case report.

作者信息

Al-Turkistani Hatim K

机构信息

Department of Pediatrics, King Fahd Hospital of the University, Al-Khobar, Saudi Arabia.

出版信息

J Family Community Med. 2008 May;15(2):91-3.

Abstract

Congenital mesoblastic nephroma (CMN) is a rare renal tumor. It can be detected antenatally especially with judicious use of ultrasonography.A premature female neonate 28 weeks' gestation, complicated by polyhydramnios, was born to a 28-year-old woman. An abdominal mass was detected antenatally. At the end of the first week of life, the newborn had hypertension that was controlled by hydralazine. Ultrasonography and CT scan showed a right-sided renal heterogeneous solid mass. Right nephrectomy was performed and the histology showed CMN.

摘要

先天性中胚层肾瘤(CMN)是一种罕见的肾肿瘤。它可以在产前被检测到,尤其是合理使用超声检查时。一名孕28周的早产女新生儿,伴有羊水过多,其母亲为一名28岁女性。产前检测到腹部有肿块。出生后第一周结束时,该新生儿出现高血压,用肼屈嗪控制。超声检查和CT扫描显示右侧肾脏有一个不均匀实性肿块。进行了右侧肾切除术,组织学检查显示为先天性中胚层肾瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e601/3377027/3449d020efe6/JFCM-15-91-g001.jpg

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