An uncommon cause of severe dysmenorrhea in a 16-year-old: accessory cavitated uterine mass
This case report describes a 16-year-old with severe dysmenorrhea successfully treated by laparoscopic excision of an accessory cavitated uterine mass identified via MRI.
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This case report describes a 16-year-old with two years of severe cyclical dysmenorrhea that did not respond to hormonal therapy, ultimately attributed to an accessory cavitated uterine mass (ACUM), a rare Müllerian anomaly. Ultrasound showed a focal left myometrial lesion with a small cystic component, and MRI demonstrated a well-defined thick-walled cystic mass with an internal blood–fluid level without communication with the endometrial cavity; laparoscopic excision identified a cavitary lesion containing thick “chocolate-colored” fluid, and histopathology confirmed a cavity lined by functional endometrium surrounded by smooth muscle. The patient had significant postoperative relief from dysmenorrhea, and the authors emphasize MRI and laparoscopy as diagnostic and definitive treatment. This paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index, noting that ACUM can be misdiagnosed as adenomyosis.
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- Accessory cavitated uterine mass (ACUM) as a miniature uterine anomaly causing severe lateralized dysmenorrhea: case series via openalex
- Accessory cavitated uterine mass: MRI features and surgical correlations of a rare but under-recognised entity via openalex
- W2034805453 via openalex
- W2082132600 via openalex
- W2132970488 via openalex
- W2345553923 via openalex
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