Faraggiana T, Grishman E, Churg J
Histopathology. 1982 May;6(3):299-307. doi: 10.1111/j.1365-2559.1982.tb02724.x.
Renal biopsies from 23 patients with the nephrotic syndrome and five patients with slight or no proteinuria were examined for the presence of cell coat of podocytes by light and electron microscopy. Of those with nephrotic syndrome, five had minimal change disease, nine focal glomerular sclerosis, six membraneous nephropathy and three amyloidosis. Colloidal iron and phosphotungstic acid stains were used for the demonstration of anionic and neutral polysaccharide components of the cell coat. On light microscopy, the colloidal iron reaction showed a reduction in intensity of the stain in glomeruli of patients with massive proteinuria, as compared to those with slight or no proteinuria. On electron microscopy, only the cell coat lining the surface of the foot processes disappeared parallel to the loss of these structures, while the coat covering the surface facing the urinary space remained unchanged with both stains.
对23例肾病综合征患者以及5例轻度蛋白尿或无蛋白尿患者的肾活检组织进行了光镜和电镜检查,以观察足细胞细胞被的存在情况。在肾病综合征患者中,5例为微小病变病,9例为局灶性肾小球硬化,6例为膜性肾病,3例为淀粉样变性。采用胶体铁染色和磷钨酸染色来显示细胞被的阴离子和中性多糖成分。光镜下,与轻度蛋白尿或无蛋白尿患者相比,大量蛋白尿患者肾小球的胶体铁反应染色强度降低。电镜下,仅足突表面的细胞被随着这些结构的消失而平行消失,而覆盖尿极表面的细胞被在两种染色下均保持不变。