ArticleCureus2025
Spontaneous Rupture of a Hydronephrotic Kidney Secondary to Congenital Ureteropelvic Junction Obstruction: A Report of a Rare Case.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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3 authors.
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Abstract
Spontaneous rupture of the pelvicalyceal system due to obstructive uropathy is a rare urological emergency. It can mimic other abdominal catastrophes and may be underrecognized, especially in young patients. We report the case of a 17-year-old male presenting with sudden-onset left flank pain, fever, and vomiting. Imaging revealed a grossly dilated left pelvicalyceal system with contrast extravasation into the perinephric space, consistent with spontaneous rupture secondary to ureteropelvic junction (UPJ) obstruction. The patient was managed surgically via open Anderson-Hynes pyeloplasty with successful resolution. This case highlights the importance of early recognition and surgical management of spontaneous renal rupture in the context of UPJ obstruction. High clinical suspicion, timely imaging, and prompt intervention are crucial to prevent morbidity.
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