Suprasellar hemanjioblastomun eşlik ettiği von Hippel-Lindau hastalığı

von Hippel-Lindau hastalığı; retinal, spinal ve serebellar hemanjioblastom, renal hücreli karsinom, feokromositoma, pankreatik kist ve tümörler, endolenfatik kese tümörleri gibi benign ve malign tümörlerin gelişimi ile karakterize kalıtsal bir hastalıktır. Epididimde ve broad ligamentte kistler ve papiller kistadenokarsinom oluşabilir. Radyolojik görüntüleme yöntemleri von Hippel-Lindau hasta- lığının tanısında, tedavisinde ve takibinde önemli bir yere sahiptir. Bu yazıda, multi-organ tutulumları olan 32 yaşındaki bir erkek hastada, von Hippel-Lindau hastalığının radyolojik bulgularını paylaşmak amaçlanmıştır

von Hippel-Lindau disease with supracerebellar hemangioblastoma

von Hippel-Lindau disease is a hereditary disorder characterized by development of benign and malignant tumours such as retinal, spinal, and cerebellar haemangioblastomas, renal cell carsinomas, phaeochromocytomas, pancreatic cysts and tumors, endolymp- hatic sac tumors. Cysts and papiller cystadenocarcinoma of the broad ligament and epididiyms may also occur. Radiologic imaging methods has an important role in the diagnosis, treatment and following of von Hippel-Lindau. In this case, we aimed to present the radiologic findings of von Hippel-Lindau disease's radiological features in a single patient 32- year-old man who had multi-organ involvements

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