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腹泻阴性溶血尿毒综合征的临床病理表现

Clinico-pathological findings in diarrhoea-negative haemolytic uraemic syndrome.

作者信息

Taylor C M, Chua C, Howie A J, Risdon R A

机构信息

Department of Nephrology, The Birmingham Children's Hospital, Birmingham, B4 6NH, UK.

出版信息

Pediatr Nephrol. 2004 Apr;19(4):419-25. doi: 10.1007/s00467-003-1385-9. Epub 2004 Feb 24.

Abstract

This is a retrospective, national clinico-pathological study of past and current patients with haemolytic uraemic syndrome not associated with diarrhoea (D- HUS). Thirty-four patients were analysed and notified by members of the British Association for Paediatric Nephrology in 1998-1999. There was a 2:1 excess of males. Ten presented in infancy. The aetiology included 5 patients with complement abnormalities, 2 patients with complications of pneumococcal infection, and 2 with malignancies. Parental consanguinity was noted in 6 patients. Five children died, 9 developed chronic renal failure, and 10 end-stage renal failure. Only 7 made full recoveries. With a single exception, the pathological findings were unlike the previously reported glomerular thrombosis that is characteristic of diarrhoea-associated HUS, or HUS complicating verocytotoxin-producing Escherichia coli infection. Early and late glomerulopathy could be distinguished. Arteriolar and arterial disease was observed in 8 and 7 patients, respectively. Arterial disease correlated with a poor outcome. The pathology of D- HUS is of prognostic value, but this study was not powered to identify specific aetiological/pathological correlations.

摘要

这是一项针对既往及当前患有无腹泻型溶血尿毒综合征(D-HUS)患者的回顾性全国临床病理研究。1998 - 1999年,英国儿科肾脏病协会成员对34例患者进行了分析和报告。男性患者比女性多一倍。10例在婴儿期发病。病因包括5例补体异常患者、2例肺炎球菌感染并发症患者和2例恶性肿瘤患者。6例患者存在父母近亲婚配情况。5名儿童死亡,9名发展为慢性肾衰竭,10名发展为终末期肾衰竭。只有7名完全康复。除1例例外,病理表现与先前报道的腹泻相关性溶血尿毒综合征或产志贺毒素大肠杆菌感染所致溶血尿毒综合征的特征性肾小球血栓形成不同。可区分早期和晚期肾小球病变。分别在8例和7例患者中观察到小动脉和动脉疾病。动脉疾病与不良预后相关。D-HUS的病理具有预后价值,但本研究规模不足以确定特定的病因/病理相关性。

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