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.
第一作者机构：[1]Capital Med Univ, Beijing Anzhen Hosp, Dept Hematol, Beijing 100029, Peoples R China
通讯作者：
通讯机构：[1]Capital Med Univ, Beijing Anzhen Hosp, Dept Hematol, Beijing 100029, Peoples R China
推荐引用方式(GB/T 7714)：
Chen Ye,Han Xue,Wang Fang,et al.A rare vascular complication in a patient with essential thrombocythaemia: spontaneous abdominal aortic dissection[J].INTERNAL MEDICINE JOURNAL.2017,47(5):589-592.doi:10.1111/imj.13407.
APA：
Chen, Ye,Han, Xue,Wang, Fang,Bai, Beibei&Wang, Yingchun.(2017).A rare vascular complication in a patient with essential thrombocythaemia: spontaneous abdominal aortic dissection.INTERNAL MEDICINE JOURNAL,47,(5)
MLA：
Chen, Ye,et al."A rare vascular complication in a patient with essential thrombocythaemia: spontaneous abdominal aortic dissection".INTERNAL MEDICINE JOURNAL 47..5(2017):589-592
