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Spinal Cord Hemangioblastoma : Diagnosis and Clinical Outcome after Surgical Treatment  

Na, Joon-Ho (Department of Neurosurgery Samsung Medical Center Sungkyunkwan University School of Medicine)
Kim, Hyeong-Soo (Department of Neurosurgery Sungmin Hospital)
Eoh, Whan (Department of Neurosurgery Samsung Medical Center Sungkyunkwan University School of Medicine)
Kim, Jong-Hyun (Department of Neurosurgery Samsung Medical Center Sungkyunkwan University School of Medicine)
Kim, Jong-Soo (Department of Neurosurgery Samsung Medical Center Sungkyunkwan University School of Medicine)
Kim, Eun-Sang (Department of Neurosurgery Samsung Medical Center Sungkyunkwan University School of Medicine)
Publication Information
Journal of Korean Neurosurgical Society / v.42, no.6, 2007 , pp. 436-440 More about this Journal
Abstract
Objective : Spinal cord hemangioblastoma is an uncommon vascular neoplasm with a benign nature and is associated with von Hippel-Lindau (VHL) disease in 20-30% of patients. Total removal of these tumors without significant neurological deficit remains a great challenge. The purpose of this study was to investigate the efficacy of VHL mutation analysis and to evaluate surgical outcome of patients with spinal cord hemangioblastomas. Methods : This study included nine patients treated for spinal cord hemangioblastomas at our institute between December 1994 and March 2006. There were four male and five female patients. Mean age was 37.8 years. The mean follow-up period was 22.4 months. Magnetic resonance imaging (MRI) of the complete neuraxis was done in all cases and VHL mutation analysis was performed in three cases for a definite diagnosis. Results : Six patients had intramedullary tumor, and the remaining patients had intradural extramedullary lesions. Five patients were associated with VHL disease. The von Hippel-Lindau mutation analysis was done in three patients and two of them showed VHL gene abnormality. Tumors were located in the cervical cord in five cases and in the thoracic cord in four cases. All patients underwent surgical intervention, and total removal was achieved in six cases. All patients showed improvement or, at least, clinically stationary state. Surgical complications did not develop in any cases. Conclusion : Spinal hemangioblastoma in this series has been safely and effectively removed via a posterior approach. Postoperatively, clinical outcome was excellent in the majority of cases. The VHL mutation analysis was useful in patients with family history and in those with multiple hemangioblastomas.
Keywords
Hemangioblastoma; Von Hippel-Lindau disease; Mutation analysis;
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1 Melmon KL, Rosen SW : Lindau's Disease. Review of the literature and study of a large kindred. Am J Med 36 : 595-617, 1964   DOI   ScienceOn
2 Yasargil MG, Antic J, Laciga R, de Preux J, Fideler RW, Boone SC : The microsurgical removal of intramedullary spinal hemangioblastomas. Report of twelve cases and a review of the literature. Surg Neurol 3 : 141-148, 1976   PUBMED
3 Humphrey JS, Klausner RD, Linehan WM : von Hippel-Lindau syndrome : hereditary cancer arising from inherited mutations of the VHL tumor suppressor gene. Cancer Treat Res 88 : 13-39, 1996   PUBMED
4 Linehan WM, Lerman MI, Zbar B : Identification of the von Hippel- Lindau (VHL) gene. Its role in renal cancer. JAMA 273 : 564-570, 1995   DOI
5 Lonser RR, Weil RJ, Wanebo JE, DeVroom HL, Oldfield EH : Surgical management of spinal cord hemangioblastomas in patients with von Hippel-Lindau disease. J Neurosurg 98 : 106-116, 2003   DOI   ScienceOn
6 Richard S, Campello C, Taillandier L, Parker F, Resche F : Haemangioblastoma of the central nervous system in von Hippel-Lindau disease. French VHL study group. J Intern Med 243 : 547-553, 1998   DOI   ScienceOn
7 Catapano D, Muscarella LA, Guarnieri V, Zelante L, D'Angelo VA, D'Agruma L : Hemangioblastomas of central nervous system : molecular genetic analysis and clinical management. Neurosurgery 56 : 1215- 1221; discussion 1221, 2005   DOI
8 Gallou C, Chauveau D, Richard S, Joly D, Giraud S, Olschwang S, et al : Genotype-phenotype correlation in von Hippel-Lindau families with renal lesions. Hum Mutat 24 : 215-224, 2004   DOI   ScienceOn
9 Richard S, David P, Marsot-Dupuch K, Giraud S, Beroud C, Resche F : Central nervous system hemangioblastomas, endolymphatic sac tumors, and von Hippel-Lindau disease. Neurosurg Rev 23 : 1-22; discussion 23-24, 2000   DOI
10 Xu QW, Bao WM, Mao RL, Yang GY : Magnetic resonance imaging and microsurgical treatment of intramedullary hemangioblastoma of the spinal cord. Neurosurgery 35 : 671-675; discussion 675-676, 1994   DOI   ScienceOn
11 Spetzger U, Gertalanffy H, Huffmann B, Mayfrank L, Reul J, Gilsbach JM : Hemangioblastomas of the spinal cord and the brainstem : diagnostic and therapeutic features. Neurosurg Rev 19 : 147-151, 1996   DOI
12 Neumann HP, Eggert HR, Scheremet R, Schumacher M, Mohadjer M, Wakhloo AK, et al : Central nervous system lesions in von Hippel- Lindau syndrome. J Neurol Neurosurg Psychiatry 55 : 898-901, 1992   DOI
13 Lee DK, Choe WJ, Kim DY, Lee CH, Chung CK, Kim HJ : Clinical analysis of spinal cord hemangioblastoma. J Korean Neurosurg Soc 30 : 1291-1299, 2001
14 Cristante L, Herrmann HD : Surgical management of intramedullary hemangioblastoma of the spinal cord. Acta Neurochir (Wien) 141 : 333-339; discussion 339-340, 1999   DOI
15 Roonprapunt C, Silvera VM, Setton A, Freed D, Epstein FJ, Jallo GI : Surgical management of isolated hemangioblastomas of the spinal cord. Neurosurgery 49 : 321-327; discussion 327-328, 2001   DOI
16 Samii M, Klekamp J : Surgical results of 100 intramedullary tumors in relation to accompanying syringomyelia. Neurosurgery 35 : 865- 873; discussion 873, 1994   DOI   ScienceOn
17 Maher ER, Yates JR, Harries R, Benjamin C, Harris R, Moore AT, et al : Clinical features and natural history of von Hippel-Lindau disease. Q J Med 77 : 1151-1163, 1990   DOI   PUBMED   ScienceOn
18 Neumann HP, Eggert HR, Weigel K, Friedburg H, Wiestler OD, Schollmeyer P : Hemangioblastomas of the central nervous system. A 10-year study with special reference to von Hippel-Lindau syndrome. J Neurosurg 70 : 24-30, 1989   DOI
19 Silver ML, Hennigar G : Cerebellar hemangioma (hemangioblastoma) : a clinicopathological review of 40 cases. J Neurosurg 9 : 484-494, 1952   DOI
20 McCormick PC, Torres R, Post KD, Stein BM : Intramedullary ependymoma of the spinal cord. J Neurosurg 72 : 523-532, 1990   DOI
21 Stolle C, Glenn G, Zbar B, Humphrey JS, Choyke P, Walther M, et al : Improved detection of germline mutations in the von Hippel- Lindau disease tumor suppressor gene. Hum Mutat 12 : 417-423, 1998   DOI   ScienceOn
22 Trost HA, Seifert V, Stolke D : Advances in diagnosis and treatment of spinal hemangioblastomas. Neurosurg Rev 16 : 205-209, 1993   DOI
23 Sora S, Ueki K, Saito N, Kawahara N, Shitara N, Kirino T : Incidence of von Hippel-Lindau disease in hemangioblastoma patients : the University of Tokyo Hospital experience from 1954-1998. Acta Neurochir (Wien) 143 : 893-896, 2001   DOI   ScienceOn
24 Browne TR, Adams RD, Roberson GH : Hemangioblastoma of the spinal cord. Review and report of five cases. Arch Neurol 33 : 435- 441, 1976   DOI   PUBMED   ScienceOn
25 Constans JP, Meder F, Maiuri F, Donzelli R, Spaziante R, de Divitiis E : Posterior fossa hemangioblastomas. Surg Neurol 25 : 269-275, 1986   DOI   ScienceOn
26 Hurth M : Intraspinal hemangioblastomas. Neurochiurgie 21 Suppl 1 : 1-136, 1975
27 Filling-Katz MR, Choyke PL, Oldfield E, Charnas L, Patronas NJ, Glenn GM, et al : Central nervous system involvement in von Hippel- Lindau disease. Neurology 41 : 41-46, 1991   DOI   PUBMED
28 Maddock IR, Moran A, Maher ER, Teare MD, Norman A, Payne SJ, et al : A genetic register for von Hippel-Lindau disease. J Med Genet 33 : 120-127, 1996   DOI
29 Glenn GM, Linehan WM, Hosoe S, Latif F, Yao M, Choyke P, et al : Screening for von Hippel-Lindau disease by DNA polymorphism analysis. JAMA 267 : 1226-1231, 1992   DOI
30 Pan L, Wang EM, Wang BJ, Zhou LF, Zhang N, Cai PW, et al : Gamma knife radiosurgery for hemangioblastomas. Stereotact Funct Neurosurg 70 Suppl 1 : 179-186, 1998   DOI   ScienceOn
31 Yasui T, Hakuba A, Katsuyama J, Nishimura S : Microsurgical removal of intramedullary spinal cord tumors : report of 22 cases. Acta Neurochir Suppl (Wein) 43 : 9-12, 1988
32 Murota T, Symon L : Surgical management of hemangioblastoma of the spinal cord : a report of 18 cases. Neurosurgery 25 : 699-707; discussion 708, 1989   DOI   PUBMED
33 Woodward ER, Buchberger A, Clifford SC, Hurst LD, Affara NA, Maher ER : Comparative sequence analysis of the VHL tumor suppressor gene. Genomics 65 : 253-265, 2000   DOI   ScienceOn
34 Rebner M, Gebarski SS : Magnetic resonance imaging of spinal-cord hemangioblastoma. AJNR Am J Neuroradiol 6 : 287-289, 1985   PUBMED
35 Latif F, Tory K, Gnarra J, Yao M, Duh FM, Orcutt ML, et al : Identification of the von Hippel-Lindau disease tumor suppressor gene. Science 260 : 1317-1320, 1993   DOI
36 Solomon RA, Stein BM : Unusual spinal cord enlargement related to intramedullary hemangioblastoma. J Neurosurg 68 : 550-553, 1988   DOI