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多脏器异常的遗传性出血性毛细血管扩张症一例

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摘要 患者男,40岁。1992年5月因打喷嚏时突然右鼻出血,量约100ml,当地医院经前鼻孔填塞后血止,以后每年右鼻常出血反复发作,出血量10~100ml,处理后血止。1996年因脑脓肿在外院行手术治疗,伴有后遗症:右手不能伸、右脚走路时不能曲,踝阵挛。1997年因反复巩膜黄染,反复右鼻出血5年,考虑肝硬化、右鼻出血收治本院消化内科治疗,
出处 《中华耳鼻咽喉头颈外科杂志》 CAS CSCD 北大核心 2008年第3期232-233,共2页 Chinese Journal of Otorhinolaryngology Head and Neck Surgery
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参考文献9

  • 1张广森.应加强对遗传性出血性毛细血管扩张症与血管生成和发育障碍的研究[J].中华医学杂志,2004,84(3):177-178. 被引量:6
  • 2Shovlin CL, Gattmacher AE, Busearini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-OslerWeber syndrome). Am J Med Genet, 2000,91:66-67.
  • 3Porteous ME, Bum J, Proctor SJ. Hereditary haemorrhagie telangiectasia: a clinical analysis. J Med Genet, 1992, 29: 527-530.
  • 4Katsinelos P, Chalzimavroudis G, Zavos C, et aL Gastric predominant hereditary hemorrhagic telangiectasia. Vasa, 2006, 35:258-261.
  • 5Cottln V, Chinet T, Lavole A, et al. Pulmonary. arteriovenous malformations in hereditary hemorrhagic telangieetasia: a series of 126 patients. Medicine ( Baltimore), 2007,86 : 1-17.
  • 6Cottin V, Plauchu H, Bayle JY, et aL Pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangieetasia. Am J Respir Crit Care Med, 2004,169:994-1000.
  • 7Shovlin CL, Letarte M. Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms. Thorax, 1999, 54 : 714-729.
  • 8Gallitelli M, Lepore V, Pasculli G, et al. Brain abscess: a need to screen for puhnonary arteriovenous malformations. Neuroepidemiology, 2005,24:76-78.
  • 9Pagella F, Semino L, Olivieri C, et aL Treatment of epistaxis in hereditary hemorrhagic telangiectasia patients by argon plasma coagulation with local anesthesia. Am J Rhinol, 2006, 20: 421-425.

二级参考文献4

  • 1Berg J,Porteous M,Reinhardt D,et al.Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotype caused by endoglin and ALK1 mutations[].Journal of Medical Genetics.2003
  • 2Johnson DW,Berg JN,Baldwin MA,et al.Mutations in the activin receptor-like kinase 1 gene in herediary haemorrhagic telangiectasia type 2[].Nature Genetics.1996
  • 3Oh SP,Seki T,Goss KA,et al.Activin receptor-like kinase 1 modulates transforming growth factor-beta 1 signaling in the regulation of angiogenesis[].Proceedings of the National Academy of Sciences of the United States of America.2001
  • 4Li DY,Sorensen LK,Brooke BS,et al.Defective angiogenesis in mice lacking endoglin[].Science.1999

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