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一名患有狼疮性肾炎的尼日利亚患者同时存在常染色体显性多囊肾病和肾病综合征。

Co-existing autosomal dominant polycystic kidney disease and nephrotic syndrome in a Nigerian patient with lupus nephritis.

作者信息

Akinbodewa A A, Adejumo O A, Ogunsemoyin A O, Osasan S A, Adefolalu O A

机构信息

Kidney Care Centre, University of Medical Sciences, Ondo State, Nigeria.

出版信息

Ann Afr Med. 2016 Apr-Jun;15(2):83-6. doi: 10.4103/1596-3519.179735.

Abstract

A little over 30 cases on co-existing nephrotic syndrome and autosomal dominant polycystic kidney disease (ADPKD) have been reported from different regions of the world since 1957. We present a case report on co-existence of nephrotic syndrome (secondary to lupus nephritis) with ADPKD in a 24-year-old woman from Nigeria. She was positive for anti-double stranded DNA. Renal histology showed International Society of Nephrology/Renal Pathology Society Class II lupus nephritis. The co-existence of nephrotic syndrome and ADPKD may have been overlooked in Africa in the past. There is a need to screen for nephrotic syndrome in patients with ADPKD among clinicians in the African setting.

摘要

自1957年以来,世界各地已报道了30多例同时患有肾病综合征和常染色体显性多囊肾病(ADPKD)的病例。我们报告了一名来自尼日利亚的24岁女性,她同时患有肾病综合征(继发于狼疮性肾炎)和ADPKD。她的抗双链DNA检测呈阳性。肾脏组织学检查显示为国际肾脏病学会/肾脏病理学会II级狼疮性肾炎。过去,肾病综合征和ADPKD的并存情况在非洲可能被忽视了。在非洲地区的临床医生中,有必要对ADPKD患者进行肾病综合征筛查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f92/5402818/7ff43b7c5af6/AAM-15-83-g001.jpg

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