A Case of Mesangial Proliferative Nephritis Caused by Slow Cryoglobulin.

IF 0.7 Q4 UROLOGY & NEPHROLOGY
Case Reports in Nephrology and Dialysis Pub Date : 2023-08-14 eCollection Date: 2023-01-01 DOI:10.1159/000531736
Seiji Hashimoto, Nobuhiko Okamoto, Tomochika Maoka, Rie Yamamoto, Shinichi Araki, Akira Suzuki, Yuichiro Fukasawa, Takao Koike
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Abstract

The patient was a woman in her 60s. She was found to have proteinuria on a health checkup. She did not have any particular subjective symptoms, and no definitive diagnosis was made, despite serological findings indicative of immune abnormalities. A renal biopsy was performed. Light microscopy of renal tissue section revealed mesangial proliferative nephritis. Electron microscopic findings included electron-dense deposits and fibrillar/tubular structures with a diameter of 20-30 nm. These findings suggested the presence of cryoglobulin (CG), but CG was not detected in qualitative or quantitative hematologic tests. Thus, the serum samples were stored at 37°C for a long period of time and then cooled to 4°C. When the obtained precipitates were examined, CG was successfully detected. CG that precipitates only after a long period of time is referred to as slow cryoglobulin (sCG), and sCG is extremely rare. The present case is the first documented case, to our knowledge, of renal disorders caused by sCG. It should be noted that there are some cases in which it takes much time for CG to precipitate. Thus, when CG cannot be detected, it is necessary to spend much time to determine whether CG precipitates.

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Abstract Image

慢冷球蛋白致系膜增生性肾炎1例
病人是一位60多岁的妇女。她在健康检查中被发现有蛋白尿。她没有任何特殊的主观症状,也没有做出明确的诊断,尽管血清学结果表明免疫异常。进行了肾活检。肾组织切片光镜检查显示系膜增生性肾炎。电子显微镜发现包括电子致密沉积物和直径为20-30 nm的原纤维/管状结构。这些发现表明存在冷冻球蛋白(CG),但在定性或定量血液学测试中未检测到CG。因此,血清样品在37°C下储存很长一段时间,然后冷却至4°C。当检查所获得的沉淀物时,成功地检测到CG。只有在长时间后才沉淀的CG被称为慢冷冻球蛋白(sCG),并且sCG极为罕见。据我们所知,本病例是第一例由sCG引起的肾脏疾病。应该注意的是,在某些情况下,CG沉淀需要很长时间。因此,当不能检测到CG时,需要花费大量时间来确定CG是否沉淀。
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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
36
审稿时长
10 weeks
期刊介绍: This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of nephrology and dialysis, including genetic susceptibility, clinical presentation, diagnosis, treatment or prevention, toxicities of therapy, critical care, supportive care, quality-of-life and survival issues. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed.
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