Review of Pancreatic Lesions in Von Hippel-Lindau Disease

• Prif Awduron: Tárcia Nogueira Ferreira Gomes (Awdur), Lívia de Almeida Costa (Awdur), Luciano Lenz (Awdur), Giovana Biasia de Sousa (Awdur), Ermelindo Della Libera (Awdur), Frank Shigueo Nakao (Awdur)
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• Cyhoeddwyd: Archives of Clinical Gastroenterology - Peertechz Publications, 2016-06-17.
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<p>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 pa...