ampulla of Vater adenocarcinoma
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Etiology
- risk factors
Pathology
- tumors may arise from bile duct, pancreatic duct or duodenum
Clinical manifestations
Laboratory
- no specific markers
- serum CA 19-9 may be elevated
- serum carcinoembryonic antigen may be elevated
Diagnostic procedures
- ERCP & endoscopic ultrasound
- tissue sampling
- decompression of obstruction via placing a stent
- upper gastrointestinal endoscopy & colonoscopy for surveillance of hereditary polyposis syndrome (familial adenomatous polyposis, Lynch syndrome)
Radiology
Management
- surgical excision (pancreaticoduodenectomy) if no evidence of advanced disease
More general terms
Additional terms
References
- ↑ Medical Knowledge Self Assessment Program (MKSAP) 15, 16, 17, 18. American College of Physicians, Philadelphia 2009, 2012, 2015, 2018.
- ↑ Heinrich S, Clavien PA. Ampullary cancer. Curr Opin Gastroenterol. 2010 May;26(3):280-5 PMID: https://www.ncbi.nlm.nih.gov/pubmed/20168227
- ↑ Askew J, Connor S Review of the investigation and surgical management of resectable ampullary adenocarcinoma. HPB (Oxford). 2013 Nov;15(11):829-38 PMID: https://www.ncbi.nlm.nih.gov/pubmed/23458317