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Updated: Jul 6, 2026

Laparoscopy-endoscopy Cooperative Surgery for the Treatment of Gastric Gastrointestinal Stromal Tumors
Published on: February 19, 2022
[Gastric fibroid polyp in a 4-month-old girl with Costello syndrome]
R Campus1, M Di Rocco, A R Sementa
1Pronto Soccorso Chirurgico, Istituto Giannina Gaslini, Genova. rixcampus@hotmail.com
Insights
A rare gastric fibroid polyp was found in an infant with Costello syndrome. This genetic disorder has a high tumor frequency, and this case marks the first documented instance of this specific tumor type.
Area of Science:
- Pediatric Gastroenterology
- Clinical Genetics
- Surgical Oncology
Background:
- Costello syndrome is a rare genetic disorder associated with a high predisposition to developing various tumors.
- Gastric fibroid polyps are uncommon benign neoplasms of the stomach.
Observation:
- A 4-month-old female infant presented with an incidentally discovered gastric fibroid polyp.
- Diagnostic imaging, including sonography and computerized tomography, confirmed the presence of the gastric lesion.
- The infant exhibited clinical features consistent with Costello syndrome.
Findings:
- The gastric fibroid polyp, a rare benign tumor, was successfully surgically excised.
- This case represents the first documented instance of a gastric fibroid polyp occurring in an individual with Costello syndrome.
Implications:
- This finding expands the spectrum of gastrointestinal manifestations associated with Costello syndrome.
- Highlights the importance of vigilant surveillance for neoplasms in patients with Costello syndrome.
- Contributes to understanding the tumorigenesis in rare genetic syndromes.
Abstract:
We describe the case of a 4-month-old girl with a gastric fibroid polyp. This was an occasional radiographic finding, confirmed by sonography and computerized tomography. This very rare benign tumor was surgically removed. The diagnosis of Costello syndrome was based on clinical appearance. This is the first report of a gastric fibroid polyp in Costello syndrome, a genetic disease with a high tumor frequency.
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