Evidence map›Paper›PMID 41815454›Full record

ArticleInternational journal of surgery case reports2026

Massive gastrointestinal stromal tumor with exophytic growth mimicking pelvic leiomyosarcoma: a case report and review of the literature.

Ahmad Al-Bitar, Mhd Ammar Zalzaleh, Hussein Al Helbawi, Maher Saifo

Abstract readCase Reports
In one paragraph

Article in International journal of surgery case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ahmad Al-BitarFaculty of Medicine, Damascus University, Damascus, Syrian Arab Republic.ORCID https://orcid.org/0009-0009-3173-1942
Mhd Ammar ZalzalehFaculty of Medicine, Damascus University, Damascus, Syrian Arab Republic.
Hussein Al HelbawiFaculty of Medicine, Damascus University, Damascus, Syrian Arab Republic.
Maher SaifoDepartment of Oncology, Damascus University, Damascus, Syrian Arab Republic.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Gastrointestinal stromal tumors (GISTs) are mesenchymal neoplasms of the gastrointestinal (GI) tract. Large, exophytically growing GISTs from the small bowel can present as massive abdominopelvic masses, creating a diagnostic challenge by mimicking primary gynecologic malignancies such as uterine leiomyosarcoma. Case Presentation: A 55-year-old woman presented with a 20-cm pelvic mass, initially diagnosed on computed tomography as a uterine leiomyosarcoma. Exploratory laparotomy, however, revealed the mass originated from the small bowel. Following resection, histopathology confirmed a malignant GIST with significant mitotic activity. The diagnosis was secured by strong immunohistochemical positivity for CD117 and DOG1. The patient remained disease-free at her 6-month follow-up. Clinical Discussion: This case highlights a critical diagnostic pitfall where a GIST's exophytic growth pattern obscures its true origin on imaging. A high index of suspicion for GIST must be maintained in the differential for any large abdominopelvic mass, regardless of its apparent source. An accurate diagnosis requires integrating surgical findings with immunohistochemical profiling, which is paramount for guiding appropriate oncologic management. Conclusion: Massive small bowel GISTs can radiologically mimic primary pelvic malignancies. This case emphasizes including GIST in the differential diagnosis of large pelvic masses, even when imaging suggests a gynecologic origin. Definitive diagnosis relies on a multidisciplinary approach to ensure accurate classification and appropriate oncologic therapy.

Indexed as

case reportexophytic growthgastrointestinal stromal tumor (GIST)leiomyosarcoma (LMS)pelvic mass

Identifiers

PMID41815454
PMCPMC12974357

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