Evidence map›Paper›PMID 42109594›Full record

ArticleClinical case reports2026

A Large Pedunculated Subserosal Leiomyoma Masquerading as a Pelvic Tumor in Early Pregnancy: A Rare Case Report.

John Lugata, Felix Luginga, Tecla Lyamuya, Glory Maringo, Eusebious Maro, Alex Mremi, Bariki Mchome

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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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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

John LugataDepartment of Obstetrics and Gynecology Kilimanjaro Christian Medical Centre Moshi Tanzania.ORCID https://orcid.org/0009-0006-9221-0452
Felix LugingaDepartment of Obstetrics and Gynecology Kilimanjaro Christian Medical Centre Moshi Tanzania.
Tecla LyamuyaDepartment of Obstetrics and Gynecology Kilimanjaro Christian Medical Centre Moshi Tanzania.
Glory MaringoDepartment of Obstetrics and Gynecology Kilimanjaro Christian Medical Centre Moshi Tanzania.
Eusebious MaroDepartment of Obstetrics and Gynecology Kilimanjaro Christian Medical Centre Moshi Tanzania.
Alex MremiSchool of Medicine KCMC University Moshi Tanzania.
Bariki MchomeDepartment of Obstetrics and Gynecology Kilimanjaro Christian Medical Centre Moshi Tanzania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

early pregnancymyomectomypedunculated subserosal leiomyomapelvic tumor

Identifiers

PMID42109594
PMCPMC13156236

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