ArticleClinical case reports2026
A Large Pedunculated Subserosal Leiomyoma Masquerading as a Pelvic Tumor in Early Pregnancy: A Rare Case Report.
Article in Clinical case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Uterine leiomyomas, commonly known as fibroids, are the most prevalent pelvic tumors in females, affecting 20%-30% of women of reproductive age. However, large pedunculated subserosal leiomyomas presenting during early pregnancy are uncommon and may mimic adnexal or intra-abdominal malignancies, posing diagnostic and management challenges. This case presents a rare example of a large pedunculated subserosal leiomyoma in early pregnancy masquerading as a pelvic tumor. This report highlights the diagnostic challenge, intraoperative findings, and successful maternal outcome following timely surgical management. Here we present a case of a 31-year-old G3 P0 + 2 L0 woman who presented to our specialty hospital in Northern Tanzania at 11 weeks and 5 days gestational age (GA). She has a history of progressive abdominal distension for 1 year, associated with abdominal pain, vomiting, nausea, and early satiety. Initial abdominal ultrasound evaluation revealed a viable intrauterine pregnancy and a large heterogeneous abdominal mass with increased vascularity on Doppler ultrasound. Magnetic resonance imaging (MRI) identified a 21 × 10 × 15 cm, well-defined encapsulated mass extending intraperitoneally, abutting major abdominal vessels, consistent with a pelvic tumor. Explorative laparotomy revealed this mass to be a pedunculated subserosal fibroid arising from the uterine fundus through a narrow vascular stalk. Myomectomy was successfully performed with minimal blood loss and histopathological examination confirmed a benign leiomyoma with cystic degeneration. The postoperative course was uneventful. Subsequent follow-up at 25 weeks GA showed a viable intrauterine pregnancy with normal fetal growth.
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