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References for Infratentorial Hemangioblastomas in Children

This page was last updated on November 25th, 2022

    1. Ammerman JM, Lonser RR, Dambrosia J, et al: Long-term natural history of hemangioblastomas in patients with von Hippel-Lindau disease: implications for treatment. J Neurosurg 105:248-255, 2006
    2. Asthagiri AR, Mehta GU, Zach L, et al: Prospective evaluation of radiosurgery for hemangioblastomas in von Hippel-Lindau disease. Neuro Oncol 12:80-86, 2010
    3. Bush ML, Prichett C, Packer M, et al: Hemangioblastoma of the cerebellopontine angle. Arch Otolaryngol Head Neck Surg 136:734-739, 2010
    4. Chang SD, Meisel JA, Hancock SL, et al: Treatment of hemangioblastomas in von Hippel-Lindau disease with linear accelerator-based radiosurgery. Neurosurgery 43:28-35, 1998
    5. Conway JE, Chou D, Clatterbuck RE, et al: Hemangioblastomas of the central nervous system in von Hippel-Lindau syndrome and sporadic disease. Neurosurgery 48:55-63, 2001
    6. Cornelius JF, Saint-Maurice JP, Bresson D, et al: Hemorrhage after particle embolization of hemangioblastomas: comparison of outcomes in spinal and cerebellar lesions. J Neurosurg 106:994-998, 2007
    7. Eschbacher J, Martirosyan ML, Nakaji P, et al: In vivo intraoperative confocal microscopy for real time histopathological imaging of brain tumors. J Neurosurg 2012 Jan 27 Epub ahead of print
    8. Frew IJ, Krek W: Multitasking by pVHL in tumour suppression. Curr Opin Cell Biol 19:685-690, 2007
    9. Gijtenbeek JM, Boots-Sprenger SH, Franke B, et al: Cyclin D1 genotype and expression in sporadic hemangioblastomas. J Neurooncol 74:261-266, 2005
    10. Glasker S, Bender BU, Apel TW, et al: The impact of genetic molecular analysis of the VHL gene in patients with hemangioblastomas of the central nervous system. J Neurol Neurosurg Psychiatry 67:758-762, 1999
    11. Glasker S, Bender BU, Apel TW, et al: Reconsideration of biallelic inactivation of the VHL tumour suppressor gene in nhemangioblastomas of the central nervous system. J Neurol Neurosurg Psychiatry 70:644-648, 2001
    12. Glasker S, Li J, Xia JB, et al: Hemangioblastomas share protein expression with embryonal hemangioblast progenitor cell. Cancer Res 66:4167-4172, 2006
    13. Hassenblatt M, Jeibmann A, Gerss J, et al: Cellular and reticular variants of haemangioblastoma revised: a clinico-pathologic study of 88 cases. Neuropathol Appl Neurobiol 31:618-622, 2005
    14. Hussein MR: Central nervous system capillary haemangioblastoma: the pathologist’s viewpoint. Int J Exp Pathol 88:311-324, 2007
    15. Jagannathan J, Lonser RR, Smith R, et al: Surgical management of cerebellar hemangioblastomas in patients with von Hippel-Lindau disease. J Neurosurg 108:210-222, 2008
    16. Jarrell ST, Vortmeyer AO, Linehan WM, et al: Metastases to hemangioblastomas in von Hippel-Lindau disease. J Neurosurg 105:256-263, 2006
    17. Julow JB, Gortval P, Pasztor E: Posterior fossa hemangioblastomas. Acta Neurochir (Wien) 128:1-4, 1994
    18. Kanno H, Kondo K, Ito S, et al: Somatic mutations of the von Hippel-Lindau tumor suppressor gene in sporadic central nervous system hemangioblastomas. Cancer Res 54:4845-4847, 1994
    19. Karabagli H, Genc A, Karabagli P, et al: Outcomes of gamma knife treatment for solid intracranial hemangioblastomas. J Clin Neurosci 17:706-710, 2010
    20. Kim WY, Kaelin WG: Role of VHL gene mutation in human cancer. J Clin Oncol 22:4991-5004, 2004
    21. Koh ES, Nichol A, Millar BA, et al: Role of fractionated external beam radiotherapy in hemangioblastoma of the central nervous system. Int J Radiat Oncol Biol Phys 69:1521-1526, 2007
    22. Kondo T, Kumabe T, Maruoka S, et al: Diagnostic value of 201Tl-single-photon emission computerized tomography studies in case of posterior fossa hemangioblastomas. J Neurosurg 95:292-297, 2001
    23. Kühne M, Sidler D, Hofer S, et al: Challenging manifestations of malignancies. Case 1. Polycythemia and high serum erythropoietin level as a result of hemangioblastoma. J Clin Oncol 22:3639-3640, 2004
    24. Latif F, Tory K, Gnarra J, et al: Identification of the von Hippel-Lindau disease tumor suppressor gene. Science 260:1317-1320, 1993
    25. Lee JY, Dong SM, Park WS, et al: Loss of heterozygosity and somatic mutations of the VHL tumor suppressor gene in sporadic cerebellar hemangioblastomas. Cancer Res 58:504-508, 1998
    26. Lee SH, Park BJ, Kim TS, et al: Long-term follow-up clinical course of cerebellar hemangioblastoma in von Hippel-Lindau disease: Two case reports and a literature review. J Korean Neurosurg Soc 48:263-267, 2010
    27. Lemeta S, Pylkkänen L, Sainio M, et al: Loss of heterozygosity at 6q is frequent and concurrent with 3p loss in sporadic and familial capillary hemangioblastomas. J Neuropathol Exp Neurol 63:1072-1079, 2004
    28. Lonser RR, Glenn GM, Walther M, et al: Von Hippel-Lindau disease. Lancet 361:2059-2067, 2003
    29. Lonser RR, Vortmeyer AO, Butman JA, et al: Edema is a precursor to central nervous system peritumoral cyst formation. Ann Neurol 58:392-399, 2005
    30. Louis DN, Ohgaki H, Wiestler OD, et al: The 2007 WHO Classification of Tumours of the Central Nervous System. Acta Neuropathol 114:97-109, 2007
    31. Maddock I, Moran A, Maher E, et al: A genetic register for Von Hippel-Lindau disease. J Med Genet 33:120-127, 1996
    32. Madhusudan S, Deplanque G, Braybrooke JP, et al: Antiangiogenic therapy for von Hippel-Lindau disease. JAMA 291:943-944, 2004
    33. Maher ER, Iselius L, Yates J, et al: Von Hippel-Lindau disease: a genetic study. J Med Genet 28:443-447, 1991
    34. Maher ER, Yates JRW, Ferguson-Smith MA: Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar hemangioblastoma and renal cell carcinoma. J Med Genet 27:311-314, 1990
    35. Moss JM, Choi CYH, Adler JR, et al: Stereotactic radiosurgical treatment of cranial and spinal hemangioblastomas. Neurosurgery 65:79-85, 2009
    36. Murai Y, Adachi K, Matano F, et al: Indocyanin green videoangiography study of hemangioblastomas. Can J Neurol Sci 38:41-47, 2001
    37. Niemelä M, Mäenpää H, Salven P: Interferon alpha-2a therapy in 18 hemangioblastomas. Clin Cancer Res 7:510-516, 2007
    38. Park DM, Zhuang Z, Chen L, et al: Von Hippel-Lindau disease-associated hemangioblastomas are derived from embryological multipotent cells. PLoS Med 4:e60, 2007
    39. Parker F, Aghakhani N, Ducati LG, et al: Results of microsurgical treatment of medulla oblongata and spinal cord hemangioblastomas: a comparison of two distinct clinical patient groups. J Neurooncol 93:133-137, 2009
    40. Pavesi G, Berlucchi S, Munari M, et al: Clinical and surgical features of lower brain stem hemangioblastomas in von Hippel-Lindau disease. Acta Neurochir (Wien) 152:287-292, 2010
    41. Pavesi G, Feletti A, Berlucchi S, et al: Neurosurgical treatment of von Hippel-Lindau-associated hemangioblastomas: benefits, risks and outcome. J Neurosurg Sci 52:29-36, 2008
    42. Piribauer M, Czech T, Dieckmann K, et al: Stabilization of a progressive hemangioblastoma under treatment with thalidomide. J Neurooncol 66:295-299, 2004
    43. Poulsen ML, Budtz-Jørgensen E, Bisgaard ML: Surveillance in von Hippel-Lindau disease (vHL). Clin Genet 77:49-59, 2010
    44. Resche F, Moisan JP, Mantoura J, et al: Haemangioblastomas, haemangioblastomatosis and von Hippel-Lindau disease. Adv Techn Stand Neurosurg 20:197-303, 1993
    45. Richard S, Campello C, Taillandier L, et al: Haemangioblastoma of the central nervous system in von Hipple-Lindau disease. J Intern Med 243:547-553, 1998
    46. Schimke RN, Collins DL, Stolle CA: von Hippel-Lindau syndrome, in Pagon RA, Bird TC, Dolan CR, Stephens K (eds): Gene Reviews (Internet). Seattle WA: University of Washington, Seattle, 1993-2000 (updated 2009 Dec 22)
    47. Schuch G, de Wit M, Höltje J, et al: Hemangioblastoma: diagnosis of von Hippel-Lindau disease and antiangiogenic treatment with SU5416. J Clin Oncol 23:3624-3626, 2005
    48. So CC, Ho LC: Polycythemia secondary to cerebellar hemangioblastoma. Am J Hematol 71:346–347, 2002
    49. Sprenger SH, Gijtenbeek JM, Wesseling P, et al: Characteristic chromosomal aberrations in sporadic cerebellar hemangioblastomas revealed by comparative genomic hybridization. J Neurooncol 52:241-247, 2001
    50. Tamburrini G, Massimi L, Caldarelli M, et al: Antibiotic impregnated external ventricular drainage and third ventriculostomy in the management of hydrocephalus associated with posterior cranial fossa tumours. Acta Neurochir (Wien) 150:1049-1055, 2008
    51. Van Velthoven V, Reinacher PC, Klisch J, et al: Treatment of intramedullary hemangioblastomas, with special attention to von Hippel-Lindau disease. Neurosurgery 53:1306-1314, 2003
    52. Vougioukas VI, Gläsker S, Hubbe U, et al: Surgical treatment of hemangioblastomas of the central nervous system in pediatric patients. Childs Nerv Syst 22:1149-1153, 2006
    53. Wanebo JE, Lonser RR, Glenn GM, et al: The natural history of central nervous system hemangioblastomas in patients with von Hippel-Lindau disease. J Neurosurg 98:82-94, 2003
    54. Weil RJ, Lonser RR, De Vroom HL, et al: Surgical management of brainstem hemangioblastomas in patients with von Hippel-Lindau disease. J Neurosurg 98:95-105, 2003
    55. Woodward ER, Wall K, Forsyth J, et al: VHL mutation analysis in patients with isolated central nervous system haemangioblastoma. Brain 130:836-842, 2007
    56. Yamashita K, Yoshiura T, Hiwatashi H et al: Arterial spin labeling of hemangioblastoma : differentiation from metastatic brain tumors based on quantitavive blood flow measurement. Neuroradiology 2011 Nov 10 Epub ahead of print
    57. Zhang Q, Ma L, Li W, et al: Von Hippel-Lindau disease manifesting disseminated leptomeningeal hemangioblastomatosis: surgery or medication? Acta Neurochir (Wien) 153:48-51, 2011
    58. Zhou J, Wang J, Li N, et al: Molecular genetic analysis of von Hippel-Lindau associated central nervous system hemangioblastoma. Pathol Int 60:452-458, 2010
    59. Zhou LF, Du G, Mao Y, et al: Diagnosis and surgical treatment of brainstem hemangioblastomas. Surg Neurol 63:307-316, 2005
    60. Von Hippel E: Vorstellung eines patienten mit einen sehr ungewohnlichen netzhaut beziehungsweise anderhautleiden. Bericht uber die 24. Versammlung der Opthalmologischen Gesellschaft in Heidleberg 24: 24, 1895
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