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致密膜内沉积病:新的病理特征

Dense intramembranous deposit disease: new pathologic features.

作者信息

Sibley R K, Kim Y

出版信息

Kidney Int. 1984 Apr;25(4):660-70. doi: 10.1038/ki.1984.71.

Abstract

The pathologic and clinical features of 16 patients with dense intramembranous deposit disease are described. By light microscopy nine patients had membranoproliferative glomerulonephritis, five had focal segmental necrotizing glomerulonephritis with segmental epithelial crescents, four of whom also had a prominent tubulointerstitial nephritis, and two had focal segmental mesangial proliferative glomerulonephritis. The patients with membranoproliferative glomerulonephritis and one with focal segmental mesangial proliferative glomerulonephritis had easily recognizable dense intramembranous deposits by optical microscopy. The patients with focal segmental necrotizing glomerulonephritis and one with focal segmental mesangial proliferative glomerulonephritis did not have recognizable peripheral loop dense intramembranous deposits even under oil immersion. In patients with membranoproliferative glomerulonephritis ultrastructural examination revealed extensive capillary wall dense intramembranous deposits. Immunofluorescence revealed diffuse double linear staining along the capillary walls and "mesangial rings" of C3. In the patients with focal segmental necrotizing glomerulonephritis and one with focal segmental mesangial proliferative glomerulonephritis the immunofluorescence study suggested a diagnosis of dense intramembranous deposit disease because of the segmental double linear staining of the capillary walls and "mesangial rings" of C3, but the diagnosis was only established by fine structural analysis where occasional peripheral loop and prominent paramesangial basement membrane dense intramembranous deposits and mesangial nodular deposits were identified. Clinical features prior to biopsy included nephrotic syndrome in eight patients, an acute nephritic syndrome in six patients, and asymptomatic proteinuria and hematuria in two patients. Five of six patients with an acute nephritic presentation had focal segmental necrotizing glomerulonephritis. The acute renal insufficiency in these patients was transitory and appeared to be related to a prominent acute tubulointerstitial nephritis present in four of the biopsy specimens. Depressed serum C3 levels were present in patients with membranoproliferative glomerulonephritis; patients with focal segmental lesions were normocomplementemic. Because of the "atypical" light microscopic features in six of our patients, we support the suggestion that membranoproliferative glomerulonephritis, type II be replaced by the term 'dense intramembranous deposit disease' for this glomerulopathy with variable clinical and histologic features.

摘要

本文描述了16例致密内皮下沉积病患者的病理和临床特征。光镜下,9例患者表现为膜增生性肾小球肾炎,5例表现为局灶节段性坏死性肾小球肾炎伴节段性上皮新月体形成,其中4例还伴有显著的肾小管间质性肾炎,2例表现为局灶节段性系膜增生性肾小球肾炎。膜增生性肾小球肾炎患者及1例局灶节段性系膜增生性肾小球肾炎患者在光学显微镜下可轻易识别致密内皮下沉积物。局灶节段性坏死性肾小球肾炎患者及1例局灶节段性系膜增生性肾小球肾炎患者即使在油镜下也未发现可识别的外周袢致密内皮下沉积物。膜增生性肾小球肾炎患者的超微结构检查显示广泛的毛细血管壁致密内皮下沉积物。免疫荧光显示沿毛细血管壁及C3的“系膜环”呈弥漫性双线性染色。局灶节段性坏死性肾小球肾炎患者及1例局灶节段性系膜增生性肾小球肾炎患者的免疫荧光研究因毛细血管壁及C3的“系膜环”呈节段性双线性染色而提示致密内皮下沉积病的诊断,但仅通过精细结构分析才得以确诊,在精细结构分析中发现了偶尔的外周袢及显著的系膜旁基底膜致密内皮下沉积物和系膜结节状沉积物。活检前的临床特征包括8例患者为肾病综合征,6例患者为急性肾炎综合征,2例患者为无症状蛋白尿和血尿。6例急性肾炎表现的患者中有5例为局灶节段性坏死性肾小球肾炎。这些患者的急性肾功能不全是短暂的,似乎与4例活检标本中存在的显著急性肾小管间质性肾炎有关。膜增生性肾小球肾炎患者血清C3水平降低;局灶节段性病变患者补体正常。由于我们的6例患者具有“非典型”光镜特征,我们支持将II型膜增生性肾小球肾炎这一术语替换为“致密内皮下沉积病”,用于描述这种具有可变临床和组织学特征的肾小球病。

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