Spontaneous ureteral rupture during pregnancy: a case report and literature review.

ABSTRACT:

Background

Spontaneous ureteral rupture is a rare and emergent urological entity, with limited literature guiding its diagnosis and management. Its non-specific presentation can lead to delayed recognition, posing risks of severe complications such as urinoma, sepsis, and renal failure. Currently, there is limited experience regarding the diagnosis and treatment of spontaneous ureteral rupture during pregnancy. Herein, we present a case to illustrate effective diagnostic and therapeutic strategies for managing this rare but potentially life-threatening condition.

Case description

We present a 38-year-old woman at 25 weeks' gestation who presented with acute left flank pain and nausea. Initial ultrasonography revealed bilateral hydronephrosis without evidence of urolithiasis.

SUBMITTER: Han G 

PROVIDER: S-EPMC12683475 | biostudies-literature | 2025 Nov

REPOSITORIES: biostudies-literature