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青年原发性血小板增多症一例

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摘要 患者女,19岁。发现血小板增高半年余,牙龈偶尔出血。体检:一般情况良好,心、肺听诊无特殊,肝、脾、浅表淋巴结未及肿大。血常规:血红蛋白125g/L,红细胞4.27×10^12/L,
作者 王琳 龚旭波
出处 《实用医技杂志》 2011年第2期224-224,F0003,共2页 Journal of Practical Medical Techniques
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参考文献4

  • 1Johansson P. Epidemiology of the myeloproliferative disorders polycytbemia vera and essential thrombocythemia. Semin Thromb Hemost, 2006, 32: 171-173.
  • 2Ding J, Komatsu H, Wakita A, et al. Familial essential throm- bocyhemia associated with a dominant-positive activating muta- tion of the c-MPL gene, which encodes for the receptor for thromboprotein. Blood, 2004, 103: 4198-4200.
  • 3Baxter E J, Scoh LM, Campbell PJ, et al. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet, 2005, 365: 1054-1061.
  • 4Thiele J, Kvasnicka HM, Orazi A, et al. Essential thrombo- cythemia. // Jaffe ES, Harris NL,Stein H, et al. World Health Organization classification of tumors: pathology and genetics of tumours of haematopoietic and lymphoid tissues. Lyon: Lyon IARC Press, 2008: 50-52.

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