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肾缺如:一种后天性疾病?

Renal agenesis: an acquired condition?

作者信息

Hitchcock R, Burge D M

机构信息

Department of Pediatric Surgery, Southampton General Hospital, Hampshire, United Kingdom.

出版信息

J Pediatr Surg. 1994 Mar;29(3):454-5. doi: 10.1016/0022-3468(94)90591-6.

Abstract

Renal agenesis is a relatively common congenital anomaly, although its etiology is unknown. It is clear that some solitary kidneys are the result of postnatal involution of multicystic dysplastic kidneys. The authors present a series of nine neonates with abnormal prenatal renal ultrasound findings; subsequent postnatal investigations showed an absent kidney. Five children had a prenatal diagnosis of multicystic dysplastic kidney (MDK) and two of hydronephrosis. In five cases (56%) there was a contralateral renal unit anomaly. It appears that MDK, and occasionally hydronephrosis, can involute prenatally, producing the postnatal appearance of renal agenesis.

摘要

肾缺如是一种相对常见的先天性异常,尽管其病因尚不清楚。很明显,一些孤立肾是多囊性发育不良肾产后退化的结果。作者报告了一系列9例产前肾脏超声检查结果异常的新生儿;随后的产后检查显示一侧肾脏缺如。5例患儿产前诊断为多囊性发育不良肾(MDK),2例为肾积水。5例(56%)存在对侧肾单位异常。看来,MDK,偶尔还有肾积水,可在产前退化,导致产后肾缺如的表现。

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