Isolated Intrinsic Ureteral Endometriosis: A Rare Presentation of Ureteral Obstruction
This case report details a rare instance of intrinsic ureteral endometriosis causing obstructive uropathy, successfully treated with ureteral resection and re-anastomosis, resulting in complete resolution and preserved renal function.
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This paper reports the first case (in the Caribbean) of isolated intrinsic ureteral endometriosis presenting in a 29-year-old woman with non-cyclical left pelvic and flank pain but no prior endometriosis history or typical endometriosis symptoms. Using contrast CT, the authors identified left hydronephrosis/hydroureter with a spiculated mass inseparable from the ureter, leading to presumptive diagnosis of ureteral endometriosis; surgery then found an isolated ureter-invading lesion with no pelvic or other-site endometriosis, and histopathology confirmed endometrial glands and stroma embedded in the ureteral muscularis with no malignancy. A limitation is that, as a single case report, it cannot establish diagnostic accuracy or comparative effectiveness of imaging or management strategies, and the discussion notes that preoperative presumptive diagnosis is often missed. This paper is centrally about endometriosis — it documents rare isolated intrinsic ureteral endometriosis causing ureteral obstruction.
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