BACKGROUND AND PURPOSE: Cerebellar hemangioblastomas (HBs) are traditionally classified into different morphologic types: cystic and. Hemangioblastomas (capilliary hemangioblastomas) are tumors of the central nervous system that originate from the vascular system usually during middle- age. The occurrence of cerebral hemangioblastoma in a patient with on Hippel-Lindau disease is very rare. In , Rochat described a cerebral hemangioblastoma.

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Asymptomatic lesions should be carefully followed up with a low threshold for surgical resection with development of new symptoms given low risks involved with surgery.

Cerebral hemangioblastoma occurring in a patient with von Hippel-Lindau disease. Abstract Supratentorial hemangioblastoma is a rare form of hemangioblastoma; little information is available regarding prognosis, treatment, and clinical characteristics, because the available literature is primarily composed of case reports and small case series.

Surgical resection is usually curative, and with large lesions may be made easier by preoperative embolization. The natural history of cerebellar hemangioblastomas in von Hippel-Lindau disease. It furthers the University’s objective of excellence in research, scholarship, and education by publishing worldwide. Hemangioblastomas are most commonly composed of stromal cells in small blood hemangioblaxtoma and usually occur in the cerebellumbrain stem or spinal cord.

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Case 3 Case 3. Glial fibrillary acidic protein in stromal cells of some capillary hemangioblastomas: The hemogram was normal 3 weeks after operation.

Hemangioblastoma – Wikipedia

Resection of suprasellar tumors by using a modified transsphenoidal approach. Case 2 Case 2. Second Admission In September,examination showed a large right retinal hemangioma, dysarthria, and dysmetria of the right arm.

In September,examination showed a large right retinal hemangioma, dysarthria, and dysmetria of the right arm. Supratentorial capillary hemangioblastoma presenting with fatal spontaneous intracerebral hemorrhage. We have reported a patient in whom a cerebral hemangioblastoma had the same gross and microscopic appearance as the several cerebellar lesions removed in preceding years.

A comprehensive systematic review of the English-language literature was performed. Vertebral arteriography demonstrated a poorly localized cerebellar mass.

Cerebral Hemangioblastoma Occurring in a Patient with von Hippel-Lindau Disease

The cerebral angioblastic neoplasm in our patient has been termed a hemangioblastoma. Cerebellar hemangioblastomas occurred in all four men. They are classed as grade one tumors under the World Health Organization ‘s classification system. You can also ceeebral through stacks with your mouse wheel or the keyboard arrow keys.

Therefore, we performed a systematic review of the literature to analyze clinical characteristics, disease progression, and surgical outcomes with respect to survival for hemangioblxstoma hemangioblastomas. On a scan, hemangioblastoma shows as a well-defined, low attenuation region in the posterior fossa with an enhancing nodule on the wall. Supratentorial cystic hemangioblastoma with infratentorial extension—a unique location and a rare infant case. Sign In or Create an Account.

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At craniotomy, a right cerebellar hemangioblastoma and cyst were identified and the tumor excised. The occurrence of cerebral hemangioblastoma in a patient with on Hemmangioblastoma disease is very rare. Immunohistochemical study of hemangioblastoma with special reference to its cytogenesis.

Hemangioblastoma

Thus, surgery has been the mainstay treatment for CNS hemangioblastomas with good outcomes. InRochat described a cerebral hemangioblastoma unassociated with a cyst occurring in a year-man with multiple cerebellar hemangioblastomas and a family history of angiomatosis. Ventriculography demonstrated a block and anterior dislocation of the aqueduct with moderate dilatation of the ventricular system.

Five percent of patients underwent postsurgical treatment with fractionated radiotherapy. Adult medulloblastoma Adult medulloblastoma. They suggested repeat imaging at this stage to document the size of the cyst and to plan tumor excision 7.

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