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Two Cases, Too Little, Too Late: Surveillance for Gastric Cancer in Patients with FAP
Marzia Varanese1, Ilario Lattina2, Flaminia Frattaroli1
1Department of Surgical Sciences, Sapienza University, Rome, Italy.
Abstract:
Familial adenomatous polyposis is an autosomal dominant disease due to a mutation in the adenomatous polyposis coli (APC) gene. The disease, characterized by the development of adenomas throughout the colon and rectum, is also associated with extracolonic manifestations including gastric fundic polyps and cancer. In this report, we describe two patients with FAP with advanced gastric adenocarcinoma who received systemic chemotherapy. We reviewed the literature published over the past two decades on gastric cancer in FAP patients to assess the clinical course of this disease. Due to its recent increased incidence in Western countries, close endoscopic surveillance to detect early gastric neoplastic lesions is recommended.
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