BACKGROUND von Hippel-Lindau disease is a dominantly inherited multi-system syndrome with neoplastic hallmarks. Pancreatic lesions associated with von Hippel-Lindau include serous cystic neoplasms, simple cysts, and neuroendocrine tumors. The combination of pancreatic neuroendocrine tumors and serous cystic neoplasms is relatively rare, and the surgical treatment of these lesions must consider ...

Introduction: Von Hippel-Lindau (VHL) syndrome is a disease characterized by the formation of tumors or cysts in many different parts body caused germline. The prevalence this autosomal dominant condition very rare. Understanding clinical manifestasion and diagnostic criteria needed.
 Case Report: Female, 22-year-old was reffered from orthopaedic department suffered blurred misalignment le...