Ishida Manna, Yamamoto Shinya, Iwashige Yohei, Miyazawa Shuma, Nakata Hirosuke, Seta Koichi, Yahata Kensei, Minamiguchi Sachiko, Endo Yoko, Mii Akiko, Shimizu Akira, Yanagita Motoko
Department of Nephrology, Kyoto University, Kyoto, Japan.
Department of Nephrology, National Hospital Organization Kyoto Medical Center, Kyoto, Japan.
Nephron. 2025;149(7):411-421. doi: 10.1159/000544709. Epub 2025 Feb 13.
Glomerular diseases with organized deposits can be classified into various etiologies. A diagnostic algorithm based on clinical and pathological findings has been proposed. However, some cases cannot be diagnosed using existing algorithms. Here, we report the case of a 77-year-old man diagnosed with membranoproliferative glomerulonephritis (MPGN) with striated ultrastructural deposits, micro-filament-like substructures with straight bands arranged in parallel in the subendothelial space by two sequential renal biopsies. His examinations and clinical findings were incompatible with known glomerular diseases with organized deposits. Dialysis was initiated 10 months after the second biopsy procedure. Furthermore, we report the first mass spectrometry analysis of laser micro-dissected glomeruli with striated ultrastructural deposits, which revealed significant levels of fibrinogen and fibronectin. Immunostaining was positive for fibrinogen, fibrin, and fibronectin in the subendothelial space. These findings suggest that the deposits were composed of a fibrin-fibronectin complex and that accumulation of these fibrin-fibronectin complexes possibly induced endothelial injury, leading to MPGN. We also reviewed the literature on the clinical and pathological characteristics of the four cases with striated ultrastructural deposits. Our investigation showed that all patients had the MPGN pattern and striated ultrastructural deposits in the subendothelial space, and all underwent hemodialysis within 3 years of renal biopsy. Clinicians should be aware of the findings of glomerulonephritis with striated ultrastructural deposits since this disease may be a new entity and has a poor prognosis.
具有有组织沉积物的肾小球疾病可分为多种病因。已提出一种基于临床和病理表现的诊断算法。然而,一些病例无法使用现有算法进行诊断。在此,我们报告一例77岁男性患者,通过两次连续肾活检诊断为伴有横纹状超微结构沉积物的膜增生性肾小球肾炎(MPGN),这些沉积物为微丝样亚结构,在内皮下间隙呈平行排列的直条带。他的检查和临床表现与已知的伴有有组织沉积物的肾小球疾病不相符。在第二次活检手术后10个月开始透析。此外,我们报告了首例对具有横纹状超微结构沉积物的激光显微切割肾小球进行的质谱分析,结果显示纤维蛋白原和纤连蛋白水平显著升高。在内皮下间隙,纤维蛋白原、纤维蛋白和纤连蛋白的免疫染色呈阳性。这些发现表明沉积物由纤维蛋白 - 纤连蛋白复合物组成,并且这些纤维蛋白 - 纤连蛋白复合物的积累可能诱导内皮损伤,导致MPGN。我们还回顾了有关4例具有横纹状超微结构沉积物病例的临床和病理特征的文献。我们的研究表明,所有患者均具有MPGN模式且在内皮下间隙有横纹状超微结构沉积物,并且所有患者在肾活检后3年内均接受了血液透析。临床医生应了解伴有横纹状超微结构沉积物的肾小球肾炎的发现,因为这种疾病可能是一种新的实体且预后较差。