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先天性肾积水患者的超微结构病理及临床分析
引用本文:党建功,刘润明,蒋小英,杨少毅,南勋义,董长安.先天性肾积水患者的超微结构病理及临床分析[J].西安交通大学学报(医学版),1998(1).
作者姓名:党建功  刘润明  蒋小英  杨少毅  南勋义  董长安
作者单位:西安第一临床医学院泌尿外科!西安,710061,西安第一临床医学院泌尿外科!西安,710061,西安第一临床医学院泌尿外科!西安,710061,西安第一临床医学院泌尿外科!西安,710061,西安第一临床医学院泌尿外科!西安,710061,西安第一临床医学院泌尿外科!西安,710061
摘    要:对38例单纯先天性肾积水肾盂输尿管连接部(UPJ)组织作透射电镜观察,结果:其主要超微结构病理改变是平滑肌细胞间有大量胶原料堆组织堆积,平滑肌细胞相互分离,肌细胞本身发育不良,胞膜皱折、锯齿状、指状突起,线粒体肿胀破坏。提示积水的原因是UPJ部位功能性梗阻。

关 键 词:肾盂输尿管连接部梗阻  细胞学  肾积水  透射电镜

ELECTRONMICROSCOPY OF URETEROPELVIC JUNCTION OF CONGENITAL HYDRONEPHROSIS
Dang Jiangong, Nan Xunyi, Jiang Xiaoying et al.ELECTRONMICROSCOPY OF URETEROPELVIC JUNCTION OF CONGENITAL HYDRONEPHROSIS[J].Journal of Xi‘an Jiaotong University:Medical Sciences,1998(1).
Authors:Dang Jiangong  Nan Xunyi  Jiang Xiaoying
Abstract:Electronmicroscopy of the UPJ specimens excised surgically was undertaken for 38 cases. The main histopathologic changes were an abundance of collagenous fiber tissues existing among smooth muscle cells. Vesicles and swelling were found in mitochondria with dysplasia of the muscle cells. The cause of congenital hydronephrosis was UPJ functional obstruction. Thus, the abnormal UPJ tissue should be as excised as possible in surgical treatment.
Keywords:obstruction of ureteropelvic junction  cellology  hydronephros  electronmicroscopy
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