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[儿童先天性畸形中远端输尿管的超微结构]

[Ultrastructure of the distal ureter in congenital malformations in childhood].

作者信息

Friedrich U, Schreiber D, Gottschalk E, Dietz W

出版信息

Z Kinderchir. 1987 Apr;42(2):94-102. doi: 10.1055/s-2008-1075561.

Abstract

Ultramicroscopical examinations were performed in ten children with reflux or obstructive megaureter. Resected parts of ureters were used for investigation in connection with reconstructive procedures. Whereas in case of an obstructive megaureter an intramural and juxtavesical localised functionless narrow ureteral segment is characterised by "nexus close contacts" and dissociation of muscle cells with interposition of fibrous tissue, progredient pathonexual changes in the sense of a reversible nexus-distension and irreversible nexus-rupture were seen in megaureters with reflux. Dissociation of muscle cells is combined with typical epithelial and adventitial pathological structures. In congenital megaureter, disturbances in the electric syncytium occur in connection with nexus injury, followed by pathological innervation. Interruption of muscle autonomy and innervation in the wall structure of such congenital ureteral malformations play an ominous role in the sequence of pathogenetic factors.

摘要

对10例反流性或梗阻性巨输尿管患儿进行了超微结构检查。切除的输尿管部分用于与重建手术相关的研究。在梗阻性巨输尿管病例中,壁内和膀胱旁局部无功能的狭窄输尿管段的特征是“紧密连接”以及肌肉细胞解离并伴有纤维组织插入,而在反流性巨输尿管中则可见到进展性的病理连接变化,即可逆性连接扩张和不可逆性连接破裂。肌肉细胞解离与典型的上皮和外膜病理结构相关。在先天性巨输尿管中,电合胞体的紊乱与连接损伤有关,随后出现病理神经支配。这种先天性输尿管畸形壁结构中肌肉自主性和神经支配的中断在发病因素序列中起着不祥的作用。

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