Ogawa T, Yorioka N, Toyota T, Kanahara K, Joarder Z H, Yamakido M, Kataoka K
2nd Department of Internal Medicine, Hiroshima University School of Medicine, Japan.
Hiroshima J Med Sci. 1992 Dec;41(4):105-10.
We report a case of congenital renal proximal tubular dysfunction (CRPTD) accompanied by IgA nephropathy. The mesangial matrix was slightly increased with depositions of IgA and C3. Podocytes contained many clear vacuoles. Cuboidal cells, as well as squamous cells, lined the parietal epithelium of Bowman's capsule, although the functional or pathological significance of the cuboidal cells is unknown. The proximal tubular cells appeared to have a less-developed apical endocytic complex, basal infoldings and fewer lysosomes. These morphological changes may reflect proximal tubular dysfunction.
我们报告了一例伴有IgA肾病的先天性肾近端小管功能障碍(CRPTD)病例。系膜基质轻度增加,伴有IgA和C3沉积。足细胞含有许多透明空泡。立方上皮细胞以及鳞状上皮细胞衬于鲍曼囊壁层上皮,尽管立方上皮细胞的功能或病理意义尚不清楚。近端小管细胞的顶端内吞复合体发育较差,基底褶较少,溶酶体也较少。这些形态学变化可能反映了近端小管功能障碍。