Uterine angiomyolipoma: a clinical analysis of 8 cases and literature review
This study analyzed the clinicopathological features, diagnosis, treatment, and prognosis of eight uterine angiomyolipoma cases, finding a low incidence in perimenopausal women with symptoms mimicking leiomyomas.
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This retrospective single-center study analyzed the clinicopathological features, diagnosis, treatment methods, and prognosis of eight patients with pathologically diagnosed uterine angiomyolipoma treated between 2008 and 2020, with a median follow-up of 72 months. Patients were mostly perimenopausal (mean age 50), and presentations were similar to uterine leiomyomas, including vaginal bleeding, menorrhagia, abdominal pain, and dysmenorrhea in one case with coexisting adenomyosis; imaging sometimes led to alternative diagnoses such as leiomyolipoma or fibroid degeneration, with surgery ranging from myomectomy to hysterectomy. The authors reported no relapses during follow-up and concluded that AML is rare, likely occurs in perimenopausal women, and should be suspected when a uterine tumor shows uneven internal echoes containing adipose tissue. This paper is centrally about endometriosis and adenomyosis-related pathology in the sense that it explicitly mentions adenomyosis as a coexisting finding in one patient’s symptoms, though its main topic is uterine angiomyolipoma.
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