Background: A double major papilla of Vater is a rare congenital anomaly with only three documented cases described in the literature. Case report: We report the case of a 19-year-old man, with chronic ulcerative pancolitis and congenital sphrerocytosis, who underwent endoscopic retrograde cholangiopancreatography because he had persistent elevation of liver enzymes and normal MRI cholangiography. During endoscopic retrograde cholangiopancreatography, a double papilla of Vater with separate drainage for the bile duct and the pancreatic duct was observed. Conclusion: Endoscopic retrograde cholangiopancreatography showed normal pancreatogram and findings compatible with sclerosing cholangitis. © 2009 Katsinelos et al; licensee BioMed Central Ltd.
CITATION STYLE
Katsinelos, P., Chatzimavroudis, G., Fasoulas, K., Katsinelos, T., Pilpilidis, I., Lazaraki, G., … Kountouras, J. (2009). Double major papilla of Vater - A rare endoscopic finding during endoscopic retrograde cholangiopancreatography: A case report. Cases Journal, 2(10). https://doi.org/10.1186/1757-1626-2-163
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