Yamanaka Masaki, Fujigaki Yoshihide, Kono Hajime, Nagura Michito, Arai Shigeyuki, Tamura Yoshifuru, Ota Tatsuru, Shibata Shigeru, Kondo Fukuo, Yamaguchi Yutaka, Uchida Shunya
Department of Internal Medicine, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashi-ku, Tokyo, Japan.
Department of Pathology, Teikyo University Hospital, 2-11-1 Kaga, Itabashi-ku, Tokyo, Japan.
CEN Case Rep. 2018 Nov;7(2):211-216. doi: 10.1007/s13730-018-0329-y. Epub 2018 Apr 18.
Autoimmune diseases are sometimes associated with immune-mediated renal diseases and cryoglobulinemia is one of the causes. Cryoglobulinemia and cryoglobulinemic glomerulonephritis associated with primary Sjögren's syndrome are most frequent condition among non-hepatitis C virus-related condition. Its typical renal manifestation shows high amount of proteinuria with microscopic hematuria and renal insufficiency. We describe a case of 72-year-old woman with Hashimoto disease, autoimmune hepatitis, Sjögren's syndrome, and immune-related pancytopenia complicated by cryoglobulinemic glomerulonephritis. Before kidney biopsy, tubulointerstitial nephritis probably due to Sjögren's syndrome was suspected because of persistent hematuria without significant proteinuria and developing mild renal dysfunction over 6 months. The developing renal dysfunction associated with isolated hematuria is uncommon in glomerular diseases. Kidney biopsy, however, revealed established membranoproliferative glomerulonephritis with subendothelial deposits consisting of tubular structures with IgM, IgG, and C3 staining. Corticosteroids plus mycophenolate mofetil therapy successfully normalized renal function. Physician should not overlook cryoglobulinemic glomerulonephritis, which is potentially poor prognosis, even if urinalysis shows only persistent isolated hematuria in patients with autoimmune diseases.
自身免疫性疾病有时与免疫介导的肾脏疾病相关,冷球蛋白血症是其中一个病因。在非丙型肝炎病毒相关的疾病中,与原发性干燥综合征相关的冷球蛋白血症和冷球蛋白血症性肾小球肾炎最为常见。其典型的肾脏表现为大量蛋白尿伴镜下血尿和肾功能不全。我们描述了一例72岁女性病例,患有桥本氏病、自身免疫性肝炎、干燥综合征和免疫相关性全血细胞减少症,并并发冷球蛋白血症性肾小球肾炎。在肾脏活检前,由于持续血尿且无明显蛋白尿,并在6个月内出现轻度肾功能不全,怀疑可能是干燥综合征所致的肾小管间质性肾炎。在肾小球疾病中,与孤立性血尿相关的肾功能不全并不常见。然而,肾脏活检显示为确诊的膜增生性肾小球肾炎,伴有由IgM、IgG和C3染色的管状结构组成的内皮下沉积物。糖皮质激素联合霉酚酸酯治疗成功使肾功能恢复正常。即使尿液分析仅显示自身免疫性疾病患者持续孤立性血尿,医生也不应忽视冷球蛋白血症性肾小球肾炎,其预后可能较差。