Human immunodeficiency virus-associated nephropathy mainly due to cellular variant of focal segmental glomerulosclerosis.

IF 0.7 Q4 UROLOGY & NEPHROLOGY CEN Case Reports Pub Date : 2025-06-01 Epub Date: 2025-03-17 DOI:10.1007/s13730-025-00979-2
Hikaru Tanimizu, Naoki Sawa, Akinari Sekine, Yuki Oba, Masayuki Yamanouchi, Eiko Hasegawa, Tatsuya Suwabe, Junichi Hoshino, Keiichi Kinowaki, Kei Kono, Kenichi Ohashi, Yukiko Kanetsuna, Kazuho Honda, Kensuke Joh, Yutaka Yamaguchi, Takehiko Wada, Yoshifumi Ubara
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Abstract

A 45-year-old man with a low titer of hepatitis B virus (HBV) was diagnosed with nephrotic syndrome. A subsequent test for human immunodeficiency virus (HIV) was positive. Kidney biopsy revealed some signs of collapsing variant of focal segmental glomerulosclerosis (FSGS), but the predominant finding was a cellular variant of FSGS. Two years after receiving tenofovir, urine protein became negative, and the patient was finally diagnosed with HIV-associated nephropathy. Collapsing variant of FSGS is considered typical of HIV-related nephropathy, but the cellular variant of FSGS in this patient represents another type. The cause of many FSGSs is often never identified, making cause-based treatment difficult. This case demonstrates that identification of the cause of FSGS can lead to treatment of FSGS.

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人类免疫缺陷病毒相关性肾病主要由局灶节段性肾小球硬化的细胞变异引起。
一名45岁男性,乙型肝炎病毒(HBV)滴度低,被诊断为肾病综合征。随后的人类免疫缺陷病毒(HIV)检测呈阳性。肾活检显示局灶节段性肾小球硬化(FSGS)的塌陷变型的一些迹象,但主要的发现是FSGS的细胞变型。服用替诺福韦两年后,尿蛋白呈阴性,最终确诊为hiv相关肾病。塌陷型FSGS被认为是hiv相关肾病的典型,但该患者的细胞型FSGS代表了另一种类型。许多fsgs的病因往往无法确定,这使得基于病因的治疗变得困难。本病例表明,确定FSGS的病因可以导致FSGS的治疗。
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来源期刊
CEN Case Reports
CEN Case Reports UROLOGY & NEPHROLOGY-
CiteScore
1.90
自引率
0.00%
发文量
80
期刊介绍: Clinical and Experimental Nephrology (CEN) Case Reports is a peer-reviewed online-only journal, officially published biannually by the Japanese Society of Nephrology (JSN).  The journal publishes original case reports in nephrology and related areas.  The purpose of CEN Case Reports is to provide clinicians and researchers with a forum in which to disseminate their personal experience to a wide readership and to review interesting cases encountered by colleagues all over the world, from whom contributions are welcomed.
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