首页> 外文期刊>Internal medicine journal >A rare vascular complication in a patient with essential thrombocythaemia: spontaneous abdominal aortic dissection
【24h】

A rare vascular complication in a patient with essential thrombocythaemia: spontaneous abdominal aortic dissection

机译:患有基本血小板血症的患者中罕见的血管并发症:自发腹主动脉夹层

获取原文
获取原文并翻译 | 示例
           

摘要

A 27-year-old woman complained of waist and back pain. Abdominal computed tomography angiography showed abdominal aortic dissection, the blood count revealed a high platelet count of 1655 x10(9)/L. Negative for JAK2V617F, CALR and MPL mutations (i.e. triple-negative), the patient was diagnosed as essential thrombocythaemia (ET) with abdominal aortic dissection and was treated with cytoreduction and antiplatelet drugs. Cases of abdominal aortic dissection in ET have not been previously reported. As such, we proposed a mechanism of abdominal aortic dissection caused by endothelial dysfunction and further emphasised appropriate management in ET with abdominal aortic dissection.
机译:一个27岁的女性抱怨腰部和背部疼痛。 腹部计算断层造影血管造影显示腹主动脉夹层,血液计数显示高血小板计数为1655×10(9)/ L. JAK2V617F,CALR和MPL突变(即三重阴性)的阴性,患者被诊断为具有腹主动脉夹层的基本血小板(ET),并用细胞凝固和抗血小板药物治疗。 ET中腹主动脉夹层的病例尚未报道。 因此,我们提出了由内皮功能障碍引起的腹主动脉夹层的机制,并进一步强调了腹主动脉夹层的适当管理。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号