Miyata J, Takebayashi S, Taguchi T, Naito S, Harada T
Nephron. 1986;44(2):115-20. doi: 10.1159/000183978.
Clinico-histological features in 32 patients with nephrotic syndrome (NS) due to focal segmental glomerulosclerosis (FSGS) were examined. Thirteen (group A1) were diagnosed as cases of FSGS within 2 years of the onset of NS, and 8 (61%) showed progressive renal dysfunction. Ten (group A2) developed FSGS more than 2 years after the onset of NS and had a favorable prognosis. Nine (group B) differed from groups A1 and A2 in that the remaining nonsclerosed glomeruli showed slight mesangial proliferation. All but 1 patient of group B developed FSGS within 2 years of the onset of NS, and the prognosis was poor. No patient studied showed a transition between groups A and B. In some patients, lipoid nephrosis preceded FSGS, in group A2. Thus, for an accurate prediction of the prognosis, FSGS should be divided into three subclasses, based on clinico-histological features.
对32例因局灶节段性肾小球硬化(FSGS)导致肾病综合征(NS)的患者的临床组织学特征进行了检查。13例(A1组)在NS发病2年内被诊断为FSGS病例,其中8例(61%)出现进行性肾功能不全。10例(A2组)在NS发病2年多后发生FSGS,预后良好。9例(B组)与A1组和A2组不同,其余未硬化的肾小球表现为轻度系膜增生。B组除1例患者外,所有患者均在NS发病2年内发生FSGS,预后较差。所研究的患者中没有显示出A组和B组之间的转变。在A2组的一些患者中,脂性肾病先于FSGS出现。因此,为了准确预测预后,应根据临床组织学特征将FSGS分为三个亚类。