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Literature DB >> 15980980

Treatment of recurrent cerebellar hemangioblastoma with external radiotherapy in a patient with von Hippel-Lindau disease: a case report and review of the literature.

Gulcin Ertas¹, Muzaffer Bedri Altundag, Ali Riza Ucer, Fatih Cankal, Kadri Altundag.

Abstract

Von Hippel-Lindau Disease, a multisystem familial cancer syndrome, is inherited as an autosomal-dominant trait. Common manifestations of the disease are retinal, cerebellar and medullary hemangioblastomas; renal cysts and carcinomas; pancreatic cysts; pheochromocytoma; and papilllary cystadenoma of the epididym. We report the case of a 40-year-old man with type I von Hippel-Lindau disease treated with external radiotherapy for recurrent cerebellar hemangioblastoma.

Entities: Disease Species

Mesh：

Year: 2005 PMID： 15980980 DOI： 10.1007/s11060-004-5179-0

Source DB: PubMed Journal: J Neurooncol ISSN： 0167-594X Impact factor: 4.130

22 in total

1. Hemangioblastomas of the central nervous system. A 10-year study with special reference to von Hippel-Lindau syndrome.

Authors: H P Neumann; H R Eggert; K Weigel; H Friedburg; O D Wiestler; P Schollmeyer
Journal: J Neurosurg Date: 1989-01 Impact factor: 5.115

Review 2. von Hippel-Lindau disease.

Authors: V Couch; N M Lindor; P S Karnes; V V Michels
Journal: Mayo Clin Proc Date: 2000-03 Impact factor: 7.616

3. Clinical features and natural history of von Hippel-Lindau disease.

Authors: E R Maher; J R Yates; R Harries; C Benjamin; R Harris; A T Moore; M A Ferguson-Smith
Journal: Q J Med Date: 1990-11

4. Cerebellar haemangioblastoma and von Hippel-Lindau disease.

Authors: S M Huson; P S Harper; M D Hourihan; G Cole; R D Weeks; D A Compston
Journal: Brain Date: 1986-12 Impact factor: 13.501

5. Stereotaxic radiosurgical ablation: an alternative treatment for recurrent and multifocal hemangioblastomas. A report of four cases.

Authors: K A Page; K Wayson; G K Steinberg; J R Adler
Journal: Surg Neurol Date: 1993-11

4. Malignant glioma arising at the site of an excised cerebellar hemangioblastoma after irradiation in a von Hippel-Lindau disease patient.

Authors: Na-Hye Myong; Bong-Jin Park
Journal: Yonsei Med J Date: 2009-08-19 Impact factor: 2.759

4 in total

Treatment of recurrent cerebellar hemangioblastoma with external radiotherapy in a patient with von Hippel-Lindau disease: a case report and review of the literature.

1. Hemangioblastomas of the central nervous system. A 10-year study with special reference to von Hippel-Lindau syndrome.

Review 2. von Hippel-Lindau disease.

3. Clinical features and natural history of von Hippel-Lindau disease.

4. Cerebellar haemangioblastoma and von Hippel-Lindau disease.

5. Stereotaxic radiosurgical ablation: an alternative treatment for recurrent and multifocal hemangioblastomas. A report of four cases.

Review 6. Von Hippel-Lindau disease: new strategies in early detection and treatment.

7. The natural history of hemangioblastomas of the central nervous system in patients with von Hippel-Lindau disease.

8. Von Hippel-Lindau disease: a genetic study.

9. Central nervous system lesions in von Hippel-Lindau syndrome.

10. Hemangioblastomas: clinical characteristics, surgical results and immunohistochemical studies.

1. Cerebellar hemangioblastoma associated with diffuse neonatal hemangiomatosis in an infant.

Review 2. Central nervous system capillary haemangioblastoma: the pathologist's viewpoint.

3. A vitronectin M381T polymorphism increases risk of hemangioblastoma in patients with VHL gene defect.

4. Malignant glioma arising at the site of an excised cerebellar hemangioblastoma after irradiation in a von Hippel-Lindau disease patient.