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先天性梗阻性尿路病和结节性肾胚基

Congenital obstructive uropathy and nodular renal blastema.

作者信息

Craver R, Dimmick J, Johnson H, Nigro M

出版信息

J Urol. 1986 Jul;136(1 Pt 2):305-7. doi: 10.1016/s0022-5347(17)44850-6.

Abstract

The occurrence of nodular renal blastema and renal dysplasia was determined in a retrospective study of 75 cases of congenital obstructive uropathy. Nodular renal blastema was present in 3 upper pole nephrectomy specimens removed as a consequence of nonfunction owing to ectopic ureterocele; none was dysplastic. A more differentiated type of nodular renal blastema was present in 3 other total nephrectomy specimens, bilateral involvement in a case of posterior urethral valves and unilateral nodular renal blastema associated with ureteral atresia. This subset of differentiated nodular renal blastema was associated with renal dysplasia.

摘要

在一项对75例先天性梗阻性尿路病的回顾性研究中,确定了结节性肾胚芽组织和肾发育异常的发生情况。因异位输尿管囊肿导致肾功能丧失而切除的3例上极肾切除标本中存在结节性肾胚芽组织;均无发育异常。在另外3例全肾切除标本中存在一种分化程度更高的结节性肾胚芽组织,1例后尿道瓣膜病患者为双侧受累,1例输尿管闭锁患者为单侧结节性肾胚芽组织。这种分化型结节性肾胚芽组织与肾发育异常相关。

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