Hopkins Jarrad A, Nguyen-Hoang Ann, Brealey John, Hissaria Pravin, Kapojos Jola
Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, South Australia.
Renal Unit, Division of Medicine, Lyell McEwin Hospital, South Australia, Australia.
Kidney Med. 2025 Apr 25;7(7):101017. doi: 10.1016/j.xkme.2025.101017. eCollection 2025 Jul.
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.
冷纤维蛋白原相关肾小球肾炎的特征是膜增生性肾小球肾炎,无免疫球蛋白沉积且具有独特的超微结构特征。本病例报告介绍了一名63岁男性,患有肾脏局限性冷纤维蛋白原相关肾小球肾炎,血浆冷纤维蛋白原水平为阴性。他的病史包括金属主动脉瓣置换和长期抗凝治疗。临床检查未发现皮肤表现或血栓形成事件。初步实验室检查显示严重肾功能不全,但血浆冷纤维蛋白原、血清冷球蛋白以及全面的自身免疫、感染和恶性肿瘤检查结果均为阴性。肾脏活检显示系膜毛细血管性肾小球肾炎伴局灶性血管炎和显著的间质纤维化,电子显微镜检查发现与冷纤维蛋白原一致的双壁微管。由于存在明显的肾脏瘢痕且无肾外表现,我们的患者未接受免疫抑制治疗。据我们所知,本病例描述了血清中未检测到冷纤维蛋白原的情况下冷纤维蛋白原相关肾小球肾炎的首例报告,诊断依赖于超微结构发现。考虑了免疫触须样肾小球肾炎等鉴别诊断,但根据形态学特征将其排除。本病例补充了关于肾脏局限性冷纤维蛋白原的有限文献,并强调了进行包括肾脏活检电子显微镜评估在内的全面检查以确定诊断的必要性。