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Von Hippel-Lindau病的研究进展 被引量:3

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摘要 Von Hippel- Lindau(VHL)病为常染色体显性遗传性肿瘤综合征,发病率为(2.50~2.80)/10 万,此病可有遗传因素及家族史,涉及多个系统,临床表现复杂、诊断困难.本病中有家族病史者可占4%~20% .Von Hippel- Lindau病患者可发生多系统的良性和恶性肿瘤,其主要临床表现及各自在von Hippel-Lindau 病患者中出现的比例为中枢神经系统血管母细胞瘤(60%~80% )、视网膜血管母细胞瘤(50%~60% )、内淋巴囊肿瘤(2%~11% )、肾细胞癌和(或)肾囊肿(30% ~60% )、嗜铬细胞瘤(11%~24% )、胰腺囊肿和肿瘤(60%~80% )、附睾囊腺瘤(20%~54% )以及阔韧带囊腺瘤(发病率不明)等.
出处 《临床神经外科杂志》 CAS 2011年第3期166-168,共3页 Journal of Clinical Neurosurgery
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参考文献11

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同被引文献41

  • 1李晓明,路秀英,Vortmeyer AO,庄正平,Lubensky IA.散发内淋巴囊瘤VHL基因位点微卫星标志杂合性丢失的研究[J].中华耳科学杂志,2003,1(1):19-21. 被引量:3
  • 2刘希光,王贵怀,李爱民,李宁,陈军,施辉,王富元.颈段髓内实质性血管母细胞瘤的诊断及显微手术策略[J].脑与神经疾病杂志,2011,19(1):60-62. 被引量:2
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  • 7Bambakidis NC, Megerian CA, Ratcheson RA. Differential grading of endolymphatic sac tumor extension by virtue of von Hippel - Lindau disease status. Otol Neurotol, 2004, 25:773-781.
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  • 9Mettu P, Agron E, Samtani S, et al. Genotype-phenotype correla- tion in ocular yon Hippel-Lindau (VHL) disease: the effect of missense mutation position on ocular VHL phenotype [ J]. Invest Ophth ahnol Vis Sci, 2010, 51 (9) : 4464-4470.
  • 10Isolan GR, Ashton-Prolla P, Reis MM, et al. Pineal region he- manginblastoma in a patient with Von Hippel-Lindau disease [ J ]. Arq Neuro Psiquiatr, 2011, 69(6) : 988.

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