Childs W J, Doak P B, Herdson P B
Pathology. 1978 Apr;10(2):113-29. doi: 10.3109/00313027809063488.
Forty-one renal biopsies from 34 patients presenting over a 7-year period with the nephrotic syndrome or significant proteinuria and considered initially to be cases of lipoid nephrosis have been reviewed, and the results correlated with clinical findings. Lipoid nephrosis was confirmed in 25 of the patients (20 males, 5 females) 6 of whom showed a small proportion of completely sclerosed glomeruli. Twenty-two of these patients were in remission at the time of review. Nine of the patients (4 males, 5 females) showed features typical of focal glomerulosclerosis; only 4 of these were in remission, 4 showed continuing proteinuria, and one had died. The study emphasizes the importance and problems of distinguishing lipoid nephrosis from focal glomerulosclerosis.
回顾了34例患者在7年期间出现肾病综合征或大量蛋白尿且最初被认为是类脂性肾病的41份肾活检标本,并将结果与临床发现进行了关联。25例患者(20例男性,5例女性)确诊为类脂性肾病,其中6例显示有一小部分肾小球完全硬化。在复查时,这些患者中有22例处于缓解期。9例患者(4例男性,5例女性)表现出局灶性肾小球硬化的典型特征;其中只有4例处于缓解期,4例持续存在蛋白尿,1例已死亡。该研究强调了区分类脂性肾病和局灶性肾小球硬化的重要性及问题。