Tokunaka S, Koyanagi T, Tsuji I, Yamada T
J Urol. 1982 Feb;127(2):238-44. doi: 10.1016/s0022-5347(17)53718-0.
We examined 23 nonrefluxing megaloureters histopathologically. In 18 ureters (group 1) the major anomalies were seen only in the ureterovesical junction, where the condition was characterized by more than well developed muscularity of the ureteral sheaths beside hitherto documented structural anomalies in the intravesical narrowed segment of the ureter. However, the ultrastructure of individual muscle cells was normal in the ureterovesical junction and the dilated portion. In the other 5 ureters (group 2) maldeveloped muscle cells scattered in large amounts of connective tissue were seen in the dilated portion, while in the nondilated narrow segment muscle structure was almost normal by light and electron microscopy. It was conjectured that the pathogenesis of megaloureter in group 2 resides not so much in the ureterovesical junction but more in the dilated ureteral wall, where the lack of actin filaments was documented. In group 1 ureteral sheaths were incriminated to have an additional role in the genesis of ureteral obstruction at the ureterovesical junction.
我们对23例无反流性巨输尿管进行了组织病理学检查。在18例输尿管(第1组)中,主要异常仅见于输尿管膀胱连接部,其特征是输尿管鞘的肌肉组织发育过度,此外输尿管膀胱内狭窄段还有此前记录的结构异常。然而,输尿管膀胱连接部和扩张段的单个肌细胞超微结构正常。在另外5例输尿管(第2组)中,在扩张段可见发育不良的肌细胞散在于大量结缔组织中,而在未扩张的狭窄段,光镜和电镜下肌肉结构基本正常。据推测,第2组巨输尿管的发病机制与其说是在输尿管膀胱连接部,不如说是在扩张的输尿管壁,在那里记录到了肌动蛋白丝的缺乏。在第1组中,输尿管鞘被认为在输尿管膀胱连接部输尿管梗阻的发生中起额外作用。