Recurrent cotyledonoid dissecting leiomyoma of the uterus: A case report

Cotyledonoid dissecting leiomyoma (CDL) is an exceptionally rare and morphologically unusual benign uterine leiomyoma. Its malignant-mimicking radiographic and intraoperative features pose a significant diagnostic challenge, often leading to misinterpretation and potentially overtreatment. This case is reported for its rarity and to highlight the critical importance of pathological recognition.

A 23-year-old female presented with a recurrent pelvic mass detected during a routine follow-up examination 2 years after the initial surgical resection of a uterine mass. The patient was asymptomatic.

Histopathological examination of both the initial and recurrent masses confirmed the diagnosis of CDL. The specimens exhibited characteristic features including intramural dissecting growth and an exophytic, cotyledon-like nodular appearance.

The patient underwent surgical excision for both the primary uterine mass and the recurrent pelvic mass.

The patient recovered well postoperatively with no complications. No evidence of disease was found at the most recent follow-up visit.

This case represents the first documented instance of recurrent CDL in China and only the second reported globally. It underscores that recurrence, although exceedingly rare, is a possible outcome for CDL. Pathological confirmation is paramount to achieve an accurate diagnosis, avoid a misdiagnosis of malignancy, and prevent unnecessary radical surgery or adjuvant therapy, thus preserving fertility and quality of life in young patients.