Matousovic K, Rossmann P, Skibová J, Drevíkovská J
Klinika nefrologie, Institutu klinické a experimentální medicíny, Praha.
Cas Lek Cesk. 1992 Mar 27;131(6):174-7.
IgA nephropathy was diagnosed in 114 biopsies from 107 patients comprising 78% men. Light microscopy revealed most frequently mild proliferative glomerulonephritis with frequent though rudimentary extracapillary proliferation (in one quarter of the biopsies). Allergic manifestations in the case-history were recorded in 14% of the patients. Almost in one third of the patients the disease started by macroscopic erythrocyturia. A typical finding in urine was predominating erythrocyturia (tens of millions in Addis sediment) over proteinuria (usually less than 1.5 g/24 h). Cumulative "renal survival rate" ten year after biopsy was 84%, the cumulative ratio of remissions was 30%. Mesangial fibrinoid deposits were found in half the patients with a severe course of the condition.
在107例患者的114份肾活检标本中诊断出IgA肾病,其中男性占78%。光镜检查最常见的是轻度增生性肾小球肾炎,伴有频繁但基本的毛细血管外增生(四分之一的活检标本中可见)。14%的患者病历中有过敏表现。近三分之一的患者以肉眼血尿起病。尿液中的典型表现是红细胞尿(艾迪计数中数以千万计)占主导,蛋白尿较少(通常低于1.5g/24小时)。活检后十年的累积“肾脏存活率”为84%,缓解累积率为30%。病情严重的患者中有一半发现系膜纤维蛋白样沉积。