Review of Pancreatic Lesions in Von Hippel-Lindau Disease

Archives of Clinical Gastroenterology
Review Article
Von Hippel-Lindaudisease (VHLD) is a rare hereditary tumor syndrome, inherited in autosomal dominant manner. Patients diagnosed with VHLD have a high risk of developing neoplasms of various organs (eyes, central nervous system, bone, kidney, adrenal glands, epididymis, broad ligament and pancreas).
http://www.peertechz.com/Clinical-Gastroenterology/pdf/ACG-2-118.pdf

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