Choi J, Jeong H J, Lee H Y, Kim P K, Lee J S, Han D S
Department of Pathology, Yonsei University College of Medicine, Seoul, Korea.
Yonsei Med J. 1990 Sep;31(3):258-63. doi: 10.3349/ymj.1990.31.3.258.
We studied 60 cases of minimal change nephrotic syndrome (MCNS) with mesangial IgA deposits occurring over a 6 year period. There were 43 adults and 17 children. Hematuria occurred in 69.0% of the adults and 88.2% of the children. Two adults and six children had gross hematuria during the course of the disease. Mesangial IgA deposits were noted in 100% of the cases, and concomitant IgG or IgM deposits were found in 78.6% of adults and 73.7% of children. The fluorescent intensity of mesangial IgA deposits was trace (+/-) to 1+ in 86.1% and 70.6% of the adults and children respectively. Most of the patients showed electron microscopic findings consistent with minimal change nephrotic syndrome. We speculate that most of our cases are variants of minimal change nephrotic syndrome but are neither IgA nephropathy nor an overlapping syndrome, and that environmental or genetic factors may be related to the deposition of IgA in these MCNS patients.
我们研究了6年间出现系膜IgA沉积的60例微小病变肾病综合征(MCNS)患者。其中成人43例,儿童17例。成人患者血尿发生率为69.0%,儿童为88.2%。两名成人和六名儿童在病程中出现肉眼血尿。所有病例均发现系膜IgA沉积,78.6%的成人和73.7%的儿童同时存在IgG或IgM沉积。成人和儿童系膜IgA沉积的荧光强度分别有86.1%和70.6%为微量(+/-)至1+。大多数患者的电子显微镜检查结果符合微小病变肾病综合征。我们推测,我们的大多数病例是微小病变肾病综合征的变异型,但既不是IgA肾病也不是重叠综合征,环境或遗传因素可能与这些MCNS患者的IgA沉积有关。