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输尿管的结构与超微结构。第三部分。先天性扩张输尿管(巨输尿管)。

Ureteral structure and ultrastructure. Part III. The congenitally dilated ureter (megaureter).

作者信息

Hanna M K, Jeffs R D, Sturgess J M, Barkin M

出版信息

J Urol. 1977 Jan;117(1):24-7. doi: 10.1016/s0022-5347(17)58324-x.

Abstract

A selected group of congenitally dilated ureters was examined under light and electron microscopy, and the findings were compared to the clinicoradiologic features of each ureter. These dilated ureters exhibit qualitative and/or quantitative muscular deficiencies. The obstructed megaureters secondary to posterior urethral valves and the megaureters with reflux show non-specific pathologic changes in response to increased work load or decompensation but infection within the ureter is detrimental to the muscle cells. The ureters in babies with prune belly syndrome suffer from reduced muscle cell population and a distinct myopathy involving the myofilaments within the muscle cells. The dysplastic ureter is morphologically and end stage ureter wherein the muscle cells are severely compromised. Whether this is an underdevelopment or exhaustion from repeated infections is a matter for speculation.

摘要

对一组先天性扩张输尿管进行了光镜和电镜检查,并将检查结果与每条输尿管的临床放射学特征进行了比较。这些扩张的输尿管存在定性和/或定量的肌肉缺陷。继发于后尿道瓣膜的梗阻性巨输尿管以及伴有反流的巨输尿管,会因工作负荷增加或失代偿而出现非特异性病理变化,但输尿管内的感染对肌肉细胞有害。患有梅干腹综合征的婴儿的输尿管,其肌肉细胞数量减少,且存在涉及肌肉细胞内肌丝的明显肌病。发育异常的输尿管处于形态学和终末期阶段,其中的肌肉细胞受到严重损害。这是发育不全还是反复感染导致的衰竭,尚有待推测。

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