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特发性肾积水患者人类病理性肾盂输尿管连接处的一些超微结构特征

Some ultrastructural aspects of human pathological pelvi-ureteric junction in idiopathic hydronephrosis.

作者信息

Faussone Pellegrini M S, Rizzo M

出版信息

J Submicrosc Cytol. 1982 Oct;14(4):697-709.

PMID:7143520
Abstract

Five surgical specimens of pelvi-ureteric junction from idiopathic hydronephrotic kidneys were obtained according to the Anderson-Hynes technique and were examined under an electron microscope. Fibrosis and marked alterations of several muscle cells were observed throughout all the specimens. Muscle cell alterations were different form cell to cell, namely: a noticeable development of the rough endoplasmic reticulum and of the Golgi apparatus, a great number of glycogen particles, a wide extension of the smooth endoplasmic reticulum and a disorganization of the filament pattern. The aforementioned alterations could be observed both in 'special' and 'typical' muscle cells; moreover, a reduction in the number and extension of cell-to cell junctions was observed in 'special' muscle cells only. It could be guessed that the modifications observed in the muscle cells and the fibrosis are responsible for the altered motile activity of the upper urinary tract and led to the clinical manifestations of idiopathic hydronephrosis. However, the muscle cell malfunction is probably extended more than in the surgically resected specimens, as in the patients studied it was documented by urodynamic data that the urine flow through the ureter was due to be a wide pelvic-ureteric plasty more than an effective peristaltic contraction of the upper urinary tract.

摘要

根据安德森 - 海恩斯技术获取了5个来自特发性肾积水肾脏的肾盂输尿管连接处手术标本,并在电子显微镜下进行检查。在所有标本中均观察到纤维化和几个肌细胞的明显改变。肌细胞改变在细胞之间各不相同,具体如下:粗面内质网和高尔基体显著发育、大量糖原颗粒、滑面内质网广泛延伸以及细丝模式紊乱。上述改变在“特殊”和“典型”肌细胞中均能观察到;此外,仅在“特殊”肌细胞中观察到细胞间连接数量减少和延伸缩短。可以推测,在肌细胞中观察到的改变和纤维化是上尿路运动活性改变的原因,并导致了特发性肾积水的临床表现。然而,肌细胞功能障碍可能比手术切除标本中的情况更为广泛,因为在研究的患者中,尿动力学数据表明,通过输尿管的尿液流动更多是由于广泛的肾盂输尿管成形术,而非上尿路有效的蠕动收缩。

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