Ureteral Structure and Ultrastructure. Part V. The Dysplastic Ureter
- 1 December 1979
- journal article
- research article
- Published by Wolters Kluwer Health in Journal of Urology
- Vol. 122 (6) , 796-798
- https://doi.org/10.1016/s0022-5347(17)56609-4
Abstract
The ureters in neonates and infants can be anatomically and functionally so severely compromised as to warrant the term dysplasia. The clinicopathologic criteria for this diagnosis are: a variable degree of dilatation on the excretory urogram and/or cystogram; poor or absent ureteral motility as observed on cine-fluoroscopy or at operation; poor muscularization and decreased muscle/connective tissue ratio under light microscopy; and small and deformed muscle cells with nexuses that are markedly decreased or absent and intracellular organelles that are poorly defined under EM. Excessive collagen and ground substance are present throughout the ureter. Although these qualitative and quantitative structural abnormalities are non-specific and can occur as a result of prenatal obstruction and postnatal infection, their severity in early postnatal life and their frequent association with dysplastic kidneys suggest congenital dysplasia as their etiology.This publication has 6 references indexed in Scilit:
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- Ureteral Structure and Ultrastructure. Part III. The Congenitally Dilated Ureter (Megaureter)Journal of Urology, 1976
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