Plasma-negative, Renal-limited Cryofibrinogen-associated Glomerulonephritis: A Unique Case Report

IF 3.2 Q1 UROLOGY & NEPHROLOGY
Jarrad A. Hopkins , Ann Nguyen-Hoang , John Brealey , Pravin Hissaria , Jola Kapojos
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Abstract

Cryofibrinogen-associated glomerulonephritis is characterized by membranoproliferative glomerulonephritis without immunoglobulin deposition and unique ultrastructural features. This case report presents a 63-year-old man with renal-limited cryofibrinogen-associated glomerulonephritis, with negative plasma cryofibrinogen levels. His medical history included metallic aortic valve replacement and long-term anticoagulation therapy. Clinical examination revealed no cutaneous manifestations or thrombotic events. Initial laboratory investigations showed severe kidney dysfunction, but negative results for plasma cryofibrinogen, serum cryoglobulin, and a comprehensive autoimmune, infective, and malignancy panel. Kidney biopsy revealed mesangiocapillary glomerulonephritis with focal vasculitis and significant interstitial fibrosis, and electron microscopy identified double-walled microtubules consistent with cryofibrinogen. Our patient was managed without immunosuppressive therapy due to significant kidney scarring and absence of extra-renal manifestations. To our knowledge, this case describes the first report of cryofibrinogen-associated glomerulonephritis in the absence of detectable cryofibrinogen in serum, with diagnosis relying on ultrastructural findings. Differential diagnoses such as immunotactoid glomerulonephritis were considered but ruled out based on morphological characteristics. This case adds to the limited literature on renal-limited cryofibrinogen and emphasizes the necessity for thorough investigation including electron microscopy assessment of kidney biopsies to ascertain the diagnosis.
血浆阴性,肾受限的低温纤维蛋白原相关性肾小球肾炎:一个独特的病例报告
低温纤维蛋白原相关性肾小球肾炎以膜增生性肾小球肾炎为特征,无免疫球蛋白沉积,具有独特的超微结构特征。这个病例报告了一个63岁的男性肾脏受限的低温纤维蛋白原相关性肾小球肾炎,血浆低温纤维蛋白原水平阴性。病史包括金属主动脉瓣置换术和长期抗凝治疗。临床检查未见皮肤表现或血栓事件。最初的实验室检查显示严重的肾功能不全,但血浆低温纤维蛋白原、血清低温球蛋白和综合自身免疫、感染和恶性肿瘤检查结果均为阴性。肾活检显示系血管毛细血管肾小球肾炎伴局灶性血管炎和明显间质纤维化,电镜检查发现双壁微管与低温纤维蛋白原一致。我们的病人没有接受免疫抑制治疗,因为他有明显的肾瘢痕,并且没有肾外表现。据我们所知,这是第一例在血清中检测不到低温纤维蛋白原的情况下,低温纤维蛋白原相关的肾小球肾炎的报告,诊断依赖于超微结构的发现。鉴别诊断如免疫球蛋白样肾小球肾炎被考虑,但基于形态学特征排除。本病例增加了关于肾限制性冷冻纤维蛋白原的有限文献,并强调了进行彻底调查的必要性,包括肾活检的电子显微镜评估以确定诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Kidney Medicine
Kidney Medicine Medicine-Internal Medicine
CiteScore
4.80
自引率
5.10%
发文量
176
审稿时长
12 weeks
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