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宫剑教授病例分享(四十六 ):误认为胶质瘤的小脑上蚓部囊实性血管母细胞瘤

1.Zahra, A. F., Ali, Y. M., Touria, B., & Khalid, H. (2020). A solitary hemangioblastoma of the posterior brain fossa: the role of radiotherapy. Pan African Medical Journal, 36.


2.Rachinger J, Buslei R, Prell J, Strauss C. Solid haemangioblastomas of the CNS: a review of 17 consecutive cases. Neurosurg Rev. 2009 Jan;32(1):37-47; discussion 47-8. 


3.Conway JE, Chou D, Clatterbuck RE, Brem H, Long DM, Rigamonti D. Hemangioblastomas of the central nervous system in von Hippel-Lindau syndrome and sporadic disease. Neurosurgery. 2001 Jan;48(1):55-62; discussion 62-3. 


4.Maddock IR, Moran A, Maher ER, Teare MD, Norman A, Payne SJ, Whitehouse R, Dodd C, Lavin M, Hartley N, Super M, Evans DG. A genetic register for von Hippel-Lindau disease. J Med Genet. 1996 Feb;33(2):120-7. 


5.Catapano, D., Muscarella, L. A., Guarnieri, V., Zelante, L., D’Angelo, V. A., & D’Agruma, L. (2005). Hemangioblastomas of Central Nervous System: Molecular Genetic Analysis and Clinical Management. Neurosurgery, 56(6), 1215–1221.


6.Fisher PG, Tontiplaphol A, Pearlman EM, Duffner PK, Hyder DJ, Stolle CA, Vortmeyer AO, Zhuang Z. Childhood cerebellar hemangioblastoma does not predict germline or somatic mutations in the von Hippel-Lindau tumor suppressor gene. Ann Neurol. 2002 Feb;51(2):257-60. 


7.Patiroglu T, Sarici D, Unal E, Yikilmaz A, Tucer B, Karakukcu M, Ozdemir MA, Canoz O, Akcakus M. Cerebellar hemangioblastoma associated with diffuse neonatal hemangiomatosis in an infant. Childs Nerv Syst. 2012 Oct;28(10):1801-5. 


8.Cheng J, Liu W, Hui X, Zhang S, Ju Y. Pediatric central nervous system hemangioblastomas: different from adult forms? A retrospective series of 25 cases. Acta Neurochir (Wien). 2017 Sep;159(9):1603-1611. 


9.Klingler JH, Gläsker S, Bausch B, Urbach H, Krauss T, Jilg CA, Steiert C, Puzik A, Neumann-Haefelin E, Kotsis F, Agostini H, Neumann HPH, Beck J. Hemangioblastoma and von Hippel-Lindau disease: genetic background, spectrum of disease, and neurosurgical treatment. Childs Nerv Syst. 2020 Oct;36(10):2537-2552.


10.Rednam SP, Erez A, Druker H, Janeway KA, Kamihara J, Kohlmann WK, Nathanson KL, States LJ, Tomlinson GE, Villani A, Voss SD, Schiffman JD, Wasserman JD. Von Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood. Clin Cancer Res. 2017 Jun 15;23(12):e68-e75.

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