A case of mid‐ureteral stricture with ipsilateral atrophic kidney in a young adult

Introduction: Most congenital ureteral strictures occur at the ureteropelvic or ureterovesical junction in children. Mid‐ureteral stricture is very rare and can cause congenital hydronephrosis. Only a few studies have reported on coexisting mid‐ureteral stricture with ipsilateral atrophic kidney in...

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Veröffentlicht in:IJU Case Reports 2023-11, Vol.6 (6), p.349-352
Hauptverfasser: Machida, Arisa, Abe, Masakazu, Ishii, Shuhei, Sekiguchi, Kie, Takahashi, Kenta, Shiomi, Ei, Maekawa, Shigekatsu, Kato, Yoichiro, Uesugi, Noriyuki, Obara, Wataru
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Sprache:eng
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Zusammenfassung:Introduction: Most congenital ureteral strictures occur at the ureteropelvic or ureterovesical junction in children. Mid‐ureteral stricture is very rare and can cause congenital hydronephrosis. Only a few studies have reported on coexisting mid‐ureteral stricture with ipsilateral atrophic kidney in young adults. Case presentation: A 16‐year‐old girl presented with repeated urinary tract infection. Computed tomography revealed a right atrophic kidney and hydroureter. Retrograde pyelography showed a mid‐ureteral stricture. Laparoscopic nephroureterectomy was performed, and histological examination revealed mid‐ureteral stricture with hyperplasia of the fibrous connective tissue and an atrophic kidney. Conclusion: Mid‐ureteral stricture in a young adult is extremely rare. Appropriate imaging studies including retrograde pyelography are necessary for accurate diagnosis of mid‐ureteral stricture.
ISSN:2577-171X
2577-171X
DOI:10.1002/iju5.12620