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Journal of the Korean Radiological Society ; : 45-48, 2002.
Artigo em Coreano | WPRIM | ID: wpr-64742

RESUMO

Von Hippel-Lindau disease is an autosomal dominant disorder characterized by the presence of multiple benign and malignant tumors including hemangioblastomas of the retina and central nervous system, pancreatic cysts and tumors, renal cell carcinomas, pheochromocytomas and epididymal cystadenomas. We report the radiologic findings of a case of von Hippel-Lindau disease, describing the family history.


Assuntos
Humanos , Carcinoma de Células Renais , Sistema Nervoso Central , Cistadenoma , Hemangioblastoma , Cisto Pancreático , Feocromocitoma , Retina , Doença de von Hippel-Lindau
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