Accessory cavitated uterine mass: A rare cause of severe dysmenorrhea

We present a rare Müllerian anomaly known as "accessory cavitated uterine mass (ACUM)," which causes severe, refractory dysmenorrhea, and review the literature. A 17-year-old patient experienced severe, cyclic left-sided pelvic pain, correlating with menstruation. Magnetic resonance imaging (MRI) revealed a cystic lesion surrounded by myometrial tissue. Medical treatment with oral contraceptives was unsuccessful. Laparoscopic excision of the mass was performed, and histopathology confirmed the diagnosis of ACUM. At six months postoperatively, she remained asymptomatic, and follow-up MRI showed a normal-appearing uterus. ACUM is a rare Müllerian anomaly that is challenging to diagnose preoperatively, even with advanced imaging. Surgical excision remains the definitive treatment. This case highlights the importance of clinicians considering Müllerian anomalies in adolescents presenting with severe dysmenorrhea.

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Publication Details

Journal
Journal of the Turkish-German Gynecological Association
Published
2026-01-22
DOI
https://doi.org/10.4274/jtgga.galenos.2025.2025-10-5
Primary Topic
Gynecological conditions and treatments
Type
article
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article

Accessory cavitated uterine mass: A rare cause of severe dysmenorrhea

Göğşen Önalan, Mehmet Coşkun, Mehmet Tunç, Esra Kuşçu et al.
Journal of the Turkish-German Gynecological Association
Gynecological conditions and treatments
article

Accessory cavitated uterine mass: A rare cause of severe dysmenorrhea

Göğşen Önalan, Mehmet Coşkun, Mehmet Tunç, Esra Kuşçu, Asuman Nihan Haberal
article en

Abstract

We present a rare Müllerian anomaly known as "accessory cavitated uterine mass (ACUM)," which causes severe, refractory dysmenorrhea, and review the literature. A 17-year-old patient experienced severe, cyclic left-sided pelvic pain, correlating with menstruation. Magnetic resonance imaging (MRI) revealed a cystic lesion surrounded by myometrial tissue. Medical treatment with oral contraceptives was unsuccessful. Laparoscopic excision of the mass was performed, and histopathology confirmed the diagnosis of ACUM. At six months postoperatively, she remained asymptomatic, and follow-up MRI showed a normal-appearing uterus. ACUM is a rare Müllerian anomaly that is challenging to diagnose preoperatively, even with advanced imaging. Surgical excision remains the definitive treatment. This case highlights the importance of clinicians considering Müllerian anomalies in adolescents presenting with severe dysmenorrhea.

Journal of the Turkish-German Gynecological Association
Başkent University (TR)
Good health and well-being
Openalex Percentile: Top 82%
Gynecological conditions and treatments
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