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C1q肾病的多样临床及组织学表现

Diverse clinical and histology presentation in c1q nephropathy.

作者信息

Malleshappa Pavan, Vankalakunti Mahesha

机构信息

Division of Nephrology, Department of Medicine, Adichunchanagiri Institute of Medical Sciences, Mandya, India.

出版信息

Nephrourol Mon. 2013 Jul 1;5(3):787-91. doi: 10.5812/numonthly.8308. Epub 2013 Jun 25.

Abstract

Patients presenting with nephrotic syndrome with or without nephritic illness rarely come across with the diagnosis of 'C1q nephropathy'. This entity is purely diagnosed with the help of immunofluorescence like IgA nephropathy. Clinical presentation is heterogenous, ranging from nephrotic range proteinuria to sub-nephrotic state; and with or without hematuria / renal insufficiency. Similarly, the concept of 'C1q nephroapthy' has periodically evolved since its original description by Jenette and Hipp in 1985. Here the pathophysiology, histologic findings / diagnostic and therapeutic options in patients with C1q nephropathy are discussed.

摘要

患有或不患有肾炎性疾病的肾病综合征患者很少被诊断为“C1q肾病”。该疾病完全像IgA肾病一样借助免疫荧光进行诊断。临床表现具有异质性,从肾病范围蛋白尿到亚肾病状态不等;伴有或不伴有血尿/肾功能不全。同样,“C1q肾病”的概念自1985年由珍妮特(Jenette)和希普(Hipp)首次描述以来也在不断演变。本文将讨论C1q肾病患者的病理生理学、组织学发现/诊断及治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04db/3830903/101e8482c0fb/num-05-787-g001.jpg

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