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A rare vascular complication in a patient with essential thrombocythaemia: spontaneous abdominal aortic dissection
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 × 109/L. Negative for JAK2V617F, CALR and MPL mutations (i.e. triple‐negative), the patient was diagnosed as ess...
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Published in: | Internal medicine journal 2017-05, Vol.47 (5), p.589-592 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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 × 109/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. |
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ISSN: | 1444-0903 1445-5994 |
DOI: | 10.1111/imj.13407 |