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[节段性肾发育不全]

[Segmental kidney dysplasia].

作者信息

Gil Salom M, García Sisamon F, Chuan Nuez P, Clar Blanch F, Santamaría Meseguer J

机构信息

Servicio de Urología, Hospital Clínico Universitario, Facultad de Medicina, Valencia, España.

出版信息

Arch Esp Urol. 1990 Apr;43(3):221-7.

PMID:2196002
Abstract

The frequency of segmental renal dysplasia was studied in 15 patients with complete pyeloureteral duplication whose anatomopathologic diagnosis of the lesions of some of the renal segments of duplication were available (14 partial nephrectomies, one open renal biopsy). Evidence of dysplasia was found in 10 cases (67%), the remaining 5 were diagnosed as having chronic pyelonephritis. All patients had a coexisting ureteric anomaly that drained the dysplastic renal segment: 6 ureteral ectopias, 3 ectopic ureteroceles, 1 vesicoureteral reflux. The clinical and pathogenic importance of the associated anomalies of the excretory tract, the diagnostic difficulties arising from the minimally- or non-functioning dysplastic renal segment, and the therapeutic modalities utilized are discussed.

摘要

对15例完全性肾盂输尿管重复畸形患者的节段性肾发育异常发生率进行了研究,这些患者的部分重复肾段病变有解剖病理学诊断结果(14例行部分肾切除术,1例行开放性肾活检)。10例(67%)发现发育异常证据,其余5例诊断为慢性肾盂肾炎。所有患者均存在引流发育异常肾段的输尿管异常:6例输尿管异位,3例输尿管囊肿异位,1例膀胱输尿管反流。讨论了排泄道相关异常的临床和致病重要性、发育异常的肾段功能轻微或无功能所带来的诊断困难以及所采用的治疗方式。

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