Jordan S C, Johnston W H, Bergstein J M
Arch Pathol Lab Med. 1978 Oct;102(10):530-3.
Hypothyroidism, microscopic hematuria, and proteinuria developed in an 11-year-old girl. A renal biopsy specimen showed increased mesangial cells and matrix with focal glomerular basement membrane thickening. Three years later, a pronounced increase in proteinuria was detected. Elevated levels of antibody to thyroid microsomal antigen and thyroglobulin were found in the serum. A renal biopsy specimen showed a pronounced increase in mesangial cells and matrix with generalized glomerular basement membrane thickening. Electron microscopic studies demonstrated granular deposits in the capillary walls and mesangium. Immunofluorescent studies revealed granular deposits of IgG, IgM, and C3, primarily on the glomerular basement membrane. By indirect immunofluorescence, granular glomerular basement membrane and mesangial staining were detected with antibody specific for thyroglobulin and thyroid microsomal antigen. These observations suggest development of immune complex glomerulonephritis mediated by thyroid antigens.
一名11岁女孩出现甲状腺功能减退、镜下血尿和蛋白尿。肾活检标本显示系膜细胞和基质增多,伴有局灶性肾小球基底膜增厚。三年后,检测到蛋白尿显著增加。血清中甲状腺微粒体抗原和甲状腺球蛋白抗体水平升高。肾活检标本显示系膜细胞和基质显著增加,伴有弥漫性肾小球基底膜增厚。电子显微镜研究显示毛细血管壁和系膜中有颗粒状沉积物。免疫荧光研究显示IgG、IgM和C3的颗粒状沉积物,主要位于肾小球基底膜上。通过间接免疫荧光法,用甲状腺球蛋白和甲状腺微粒体抗原特异性抗体检测到颗粒状肾小球基底膜和系膜染色。这些观察结果提示由甲状腺抗原介导的免疫复合物性肾小球肾炎的发生。