نتایج جستجو برای: von hippel lindau syndrome
تعداد نتایج: 713978 فیلتر نتایج به سال:
mal cells and a subependymal plate composed of glial cells. Accordingly, these layers give rise to ependymomas, subependymomas, and subependymal giant cell astrocytomas (1). Hemangioblastomas are benign vascular tumors with an uncertain origin. They account for 12% of all intracranial tumors, and are a component of the von Hippel-Lindau syndrome in 30% of cases (2, 3). Hemangioblastomas usually...
INTRODUCTION Pheochromocytoma is a catecholamine-secreting tumor, which is seen rarely in children. These tumors predominantly secrete norepinephrine and epinephrine. They might be familial and associated with hereditary tumors such as Von Hippel-Lindau syndrome and multiple endocrine neoplasia type II. CASE PRESENTATION The child might present with a spectrum of clinical manifestation includ...
von Hippel-Lindau (VHL) disease is an autosomal dominant inherited tumor syndrome associated with mutations of the VHL tumor suppressor gene located on chromosome 3p25. The loss of functional VHL protein contributes to tumorigenesis. This condition is characterized by development of benign and malignant tumors in the central nervous system (CNS) and the internal organs, including kidney, adrena...
Incidentally discovered adrenal masses (incidentalomas) are common and present challenges both in diagnosis and management. When incidentally discovered adrenal masses are bilateral, a refined diagnostic approach is warranted since bilateral disease is more likely to be pathologic. We review a case of a 34-year-old man with incidentally discovered bilateral adrenal nodules. A comprehensive diag...
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