GI Endoscopy · 1 min read

Vanek Tumor of the Stomach

A sessile 18 to 20 mm antral polyp in a 50-year-old woman. Endoscopic mucosal resection with clip closure, and immunohistochemistry (CD34 positive, CD117 and DOG1 negative) that ruled out GIST.

Figure 1: Vanek tumor of the stomach. (A) Initial endoscopic view of the sessile antral polyp, approximately 18-20 mm in size.

Experienced teaching points

Clinical Pearls

  1. Vanek tumors are benign gastrointestinal stromal lesions linked to PDGFRA gene mutations.
  2. Gastric Vanek tumors over 1.5 cm typically warrant endoscopic resection.
  3. Immunohistochemistry is essential to differentiate Vanek tumors from GIST, with CD34 positivity and CD117/DOG1 negativity characteristic of Vanek tumors.
  4. Endoscopic mucosal resection is a safe and effective treatment for gastric Vanek tumors.
  5. The classic microscopic finding is an onion-skin pattern of spindle cells around blood vessels with eosinophilic infiltration.

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Final Diagnosis

Gastric inflammatory fibroid polyp (Vanek tumor), resected via endoscopic mucosal resection.

Patient Demographics

A 50-year-old female patient.

Clinical History

The patient presented with epigastric abdominal pain. An upper endoscopy was performed to investigate the symptoms.

Endoscopic Findings

Endoscopy revealed a sessile polyp in the antrum, approximately 18 to 20 mm in size.

Endoscopic Technique

  1. The lesion was injected with a mixture of saline and blue dye.
  2. Endoscopic mucosal resection was performed.
  3. The post-resection defect was closed with a clip.

Discussion

Inflammatory fibroid polyps, also known as Vanek tumors, can occur throughout the gastrointestinal tract, most commonly in the stomach (approximately two-thirds of cases), followed by the ileum.

Initially considered inflammatory lesions, these are now recognized as true benign tumors due to an activating mutation of the PDGFRA gene (platelet-derived growth factor receptor alpha).

Microscopically, these polyps exhibit a classic onion-skin pattern, characterized by spindle cells whorling around prominent small blood vessels, alongside abundant eosinophils.

Most Vanek tumors are asymptomatic. However, some can lead to symptoms such as chronic abdominal pain, dyspepsia, bleeding, iron deficiency anemia, and, if in the small bowel, intussusception and bowel obstruction.

Asymptomatic and small polyps do not require specific therapy. However, polyps larger than 15-20 mm in the stomach or larger than 10 mm in the bowel warrant removal.

Endoscopic resection is the preferred therapeutic approach, as demonstrated in this case.

Immunohistochemistry was crucial for diagnosis, showing positivity for CD34 and negativity for CD117 (c-KIT negative) and DOG1, effectively ruling out a gastrointestinal stromal tumor (GIST).

References

  1. Vanek J. Gastric submucosal granuloma with eosinophilic infiltration. Am J Pathol. 1949;25(3):397-411.
  2. Daum O, Hatlova J, Mandys V, et al. Comparison of morphological, immunohistochemical, and molecular genetic features of inflammatory fibroid polyps (Vanek's tumors). Virchows Arch. 2010;456(5):491-497.

About the authors

Andrés Gutiérrez Moreira

Andrés Gutiérrez Moreira, MD

Gastroenterology Fellow, Universidad de la República (Uruguay); Visiting Fellow, Virginia Tech Carilion School of Medicine

Hospital de Clínicas, Universidad de la República, Montevideo, Uruguay

Andrés Gutiérrez Moreira, MD, is a gastroenterology fellow at the Clínica de Gastroenterología "Prof. Carolina Olano" at Hospital de Clínicas, Universidad de la República in Montevideo, Uruguay, and was a visiting fellow at Virginia Tech Carilion School of Medicine in 2025. He earned his medical degree from the Universidad de la República in 2023 and is a member of the American Society for Gastrointestinal Endoscopy and the Sociedad Uruguaya de Endoscopía Digestiva.

More articles by Andrés

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