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兄弟姐妹中的多囊肾。

Multicystic kidney in siblings.

作者信息

Moazin M S, Ahmed S, Fouda-Neel K

机构信息

Department of Surgery, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

出版信息

J Pediatr Surg. 1997 Jan;32(1):119-20. doi: 10.1016/s0022-3468(97)90114-7.

Abstract

Two siblings (one girl and one boy), with a left multicystic kidney in whom a renal abnormality had been recognized prenatally, are reported. A large renal mass was present in both patients and the second sibling also had hypertension. Early surgical resection was carried out with satisfactory clinical progress and resolution of the hypertension. Multicystic kidney is considered a developmental abnormality with a sporadic incidence. These cases and other reports of familial incidence in the literature indicate that there may also be a genetic basis for the abnormality.

摘要

报告了两名患有左多囊肾的兄弟姐妹(一女一男),他们的肾脏异常在产前就已被发现。两名患者均存在巨大肾脏肿块,第二名兄弟姐妹还患有高血压。早期进行了手术切除,临床进展令人满意,高血压也得到缓解。多囊肾被认为是一种散发性的发育异常。这些病例以及文献中其他家族性发病的报告表明,这种异常可能也有遗传基础。

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