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Ampullary cancer
Background
Overview
Definition
Ampullary cancer is a rare malignancy that originates in the ampulla of Vater.
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Pathophysiology
The pathophysiology of ampullary cancer is complex and involves a variety of molecular alterations. The most common subtype is adenocarcinoma, which can have either intestinal or pancreatobiliary differentiation. Genomic sequencing has identified several driver genes, including ELF3, TP53, KRAS, and APC, that play a role in the development of this cancer.
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Epidemiology
The incidence of ampullary cancer in the Unites States is estimated at 0.59 per 100,000 person-years.
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Disease course
Clinically, patients with ampullary cancer often present with symptoms such as jaundice, abdominal pain, weight loss, and pale stools. In some cases, the disease may be asymptomatic and detected incidentally during routine medical examinations.
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Prognosis and risk of recurrence
The prognosis of ampullary cancer varies widely and is influenced by factors such as disease stage at diagnosis, histopathological subtype, and the presence of lymph node metastases. Early detection and intervention can significantly improve survival rates.
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Guidelines
Key sources
The following summarized guidelines for the evaluation and management of ampullary cancer are prepared by our editorial team based on guidelines from the American Society for Gastrointestinal Endoscopy (ASGE 2021,2013) and the European Society of Gastrointestinal Endoscopy (ESGE 2021).
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