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成人多囊肾的超微结构肾小管基底膜病变

Ultrastructural tubular basement membrane lesions in adult polycystic kidney disease.

作者信息

Katz S K, Hakki A, Miller A S, Finkelstein S D

机构信息

Department of Pathology and Laboratory Medicine, Hahnemann University School of Medicine, Philadelphia, PA 19102.

出版信息

Ann Clin Lab Sci. 1989 Sep-Oct;19(5):352-9.

PMID:2802515
Abstract

The pathogenesis of adult polycystic kidney disease (PCKD) remains an enigma. In an attempt to find a defect that might explain the cyst formation, an ultrastructural study was performed on seven fresh bilateral nephrectomies of seven patients suffering from adult PCKD. Marked electron microscopic changes of the tubular basement membranes were detected, including thickening, splitting, fraying, and multilayering of the basement membranes. By contrast, glomerular basement membranes lacked these alterations. The kidneys from two control groups (five donor kidneys harvested for transplantation; 10 patients who suffered from end stage renal disease) showed none of the lesions detected in the polycystic kidneys. The lesions of the tubular basement membrane, the principal support of tubular wall, may be the primary phenotypic expression and cause of the inherited defect.

摘要

成人多囊肾病(PCKD)的发病机制仍是一个谜。为了寻找一个可能解释囊肿形成的缺陷,对7例患有成人PCKD的患者的7个新鲜双侧肾切除术标本进行了超微结构研究。检测到肾小管基底膜有明显的电子显微镜变化,包括基底膜增厚、分裂、磨损和多层化。相比之下,肾小球基底膜没有这些改变。两个对照组的肾脏(5个用于移植的供体肾脏;10例终末期肾病患者)均未显示多囊肾中检测到的病变。作为肾小管壁主要支撑结构的肾小管基底膜病变,可能是遗传性缺陷的主要表型表达和原因。

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