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镰状细胞肾小球病伴局灶节段性肾小球硬化

Sickle cell glomerulopathy with focal segmental glomerulosclerosis.

作者信息

Verani R R, Conley S B

机构信息

Department of Pathology and Laboratory Medicine, University of Texas Medical School, Houston.

出版信息

Child Nephrol Urol. 1991;11(4):206-8.

PMID:1777902
Abstract

Sickle cell disease is known to cause glomerulopathy, including focal segmental glomerulosclerosis (FSGS). Patients who have sickle cell glomerulopathy with FSGS are thought to have a poorer prognosis than patients who have sickle cell glomerulopathy without this lesion. The former patients are more likely to have persistent proteinuria and eventually develop end-stage renal disease. We present a boy with sickle cell glomerulopathy and FSGS who is younger than patients with similar findings reported previously. The histopathology of his renal lesions is remarkable for segmental ultrastructural changes in the glomerular basement membranes and endothelial cells. We speculate that these changes are precursory to the pathogenesis of glomerular sclerosis in patients with sickle cell disease.

摘要

已知镰状细胞病会导致肾小球病变,包括局灶节段性肾小球硬化(FSGS)。患有伴有FSGS的镰状细胞肾小球病变的患者被认为比没有这种病变的镰状细胞肾小球病变患者预后更差。前者更易出现持续性蛋白尿,并最终发展为终末期肾病。我们报告了一名患有镰状细胞肾小球病变和FSGS的男孩,他比之前报道的有类似表现的患者年龄更小。其肾脏病变的组织病理学表现为肾小球基底膜和内皮细胞的节段性超微结构改变,十分显著。我们推测这些改变是镰状细胞病患者肾小球硬化发病机制的先兆。

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