Evidence map›Paper›PMID 42394996›Full record

ArticleJournal of cancer & allied specialties2026

Diagnostic Challenge of Gastric Glomangioma Mimicking Gastrointestinal Stromal Tumor: A Case Report.

Muhammad Imran, Sameen Bin Naeem, Nahel Chaudhry, Saad Ehsan, Muhammad Awais Majeed

Abstract read
In one paragraph

Article in Journal of cancer & allied specialties, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Muhammad ImranSKMCH&RC: Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, Punjab PAKISTAN.
Sameen Bin NaeemSKMCH&RC: Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, Punjab PAKISTAN.
Nahel ChaudhrySKMCH&RC: Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, Punjab PAKISTAN.
Saad EhsanSKMCH&RC: Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, Punjab PAKISTAN.
Muhammad Awais MajeedSKMCH&RC: Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, Punjab PAKISTAN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Gastric glomus tumors (GGTs) are rare benign mesenchymal neoplasms of the stomach, often mistaken preoperatively for more common submucosal lesions such as gastrointestinal stromal tumors (GISTs). Accurate diagnosis requires a combination of endoscopic ultrasonography, histopathology, and immunohistochemistry. Case Description: We report a 51-year-old female with a two-year history of epigastric burning, anorexia, and unexplained weight loss. Initial evaluation included EUS, which identified a 1.8 × 2.4 cm hypoechoic submucosal lesion arising from the muscularis propria at the gastric antrum. Contrast-enhanced CT demonstrated a 2 cm avidly enhancing antral lesion with persistent venous-phase enhancement; no evidence of lymphadenopathy or metastasis was noted. Subsequent EUS-guided fine-needle biopsy (FNB) demonstrated an epithelioid neoplasm. Initial immunohistochemistry excluded GIST (CD117-, DOG1-), leiomyoma (desmin-), and schwannoma (S100-). Additional glomus tumor-specific markers were not performed at this stage due to limited biopsy material and a stepwise diagnostic approach. Given the peri-pancreatic location, diagnostic uncertainty, and lesion size exceeding 2 cm, the decision was made to proceed with laparoscopic distal gastrectomy. Final histopathology confirmed glomangioma, positive for SMA and vimentin; Ki-67 ~1%; 0 mitoses per 50 high-power fields (HPF); no atypia, necrosis, lymphovascular invasion, or clear margins. Postoperative surveillance CTs showed no recurrence; no adjuvant therapy was indicated. Conclusion: This case highlights the clinical and radiologic overlap between GGT and other submucosal gastric lesions. Comprehensive immunohistochemistry and careful surgical planning are essential for accurate diagnosis and management.

Indexed as

gastric glomus tumorgastrointestinal stromal tumorglomangiomaimmunohistochemistrysubmucosal gastric mass

Identifiers

PMID42394996
PMCPMC13323606

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