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Hypocalcemia: a rare complication of von Hippel-Lindau disease
P Billen1, D Vanderschueren, D Blockmans
1Dienst Algemeen Inwendige Geneeskunde, Universitair Ziekenhuis Gasthuisberg, Leuven, België.
Abstract:
von Hippel-Lindau disease is a hereditary neoplastic syndrome, characterized by malignant and benign lesions in multiple organs. Pancreatic involvement is very common and is in general asymptomatic. We describe a case of malabsorption with severe hypocalcemia in a patient with von Hippel-Lindau disease, caused by exocrine pancreatic insufficiency, probably due to severe cystic transformation of the pancreas.
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