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BMJ Case Rep. 2010 Aug 3;2010:bcr0920092234. doi: 10.1136/bcr.09.2009.2234.
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本文引用的文献

1
Advances in understanding and management of myeloproliferative neoplasms.骨髓增殖性肿瘤的认识与管理进展
CA Cancer J Clin. 2009 May-Jun;59(3):171-91. doi: 10.3322/caac.20009. Epub 2009 Apr 15.
2
Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: recommendations from an ad hoc international expert panel.世界卫生组织真性红细胞增多症、原发性血小板增多症和原发性骨髓纤维化诊断标准修订提案及理由:一个特设国际专家小组的建议
Blood. 2007 Aug 15;110(4):1092-7. doi: 10.1182/blood-2007-04-083501. Epub 2007 May 8.
3
When and how to treat essential thrombocythemia.何时以及如何治疗原发性血小板增多症。
N Engl J Med. 2005 Jul 7;353(1):85-6. doi: 10.1056/NEJMe058093.
4
Hydroxyurea compared with anagrelide in high-risk essential thrombocythemia.羟基脲与阿那格雷治疗高危原发性血小板增多症的比较。
N Engl J Med. 2005 Jul 7;353(1):33-45. doi: 10.1056/NEJMoa043800.
5
Diagnostic criteria and prognosis in polycythemia vera and essential thrombocythemia.真性红细胞增多症和原发性血小板增多症的诊断标准及预后
Semin Hematol. 1999 Jan;36(1 Suppl 2):9-13.
6
Pathogenetic mechanisms in chronic myeloproliferative disorders: polycythemia vera, essential thrombocythemia, agnogenic myeloid metaplasia, and chronic myelogenous leukemia.慢性骨髓增殖性疾病的发病机制:真性红细胞增多症、原发性血小板增多症、特发性骨髓化生及慢性粒细胞白血病。
Semin Hematol. 1999 Jan;36(1 Suppl 2):3-8.
7
Experience of the Polycythemia Vera Study Group with essential thrombocythemia: a final report on diagnostic criteria, survival, and leukemic transition by treatment.
Semin Hematol. 1997 Jan;34(1):29-39.
8
Acute myocardial infarction with essential thrombocythemia in a young man.一名年轻男性患急性心肌梗死合并原发性血小板增多症。
Am Heart J. 1983 Aug;106(2):406-7. doi: 10.1016/0002-8703(83)90213-2.

一名接受心肌梗死治疗的年轻男性的原发性血小板增多症。

Essential thrombocythemia in a young man treated for myocardial infarction.

作者信息

Pande S, Joshi R, Pande R

机构信息

Department of Rehabilitation Medicine, Changi General Hospital, Singapore.

出版信息

BMJ Case Rep. 2010 Aug 3;2010:bcr0920092234. doi: 10.1136/bcr.09.2009.2234.

DOI:10.1136/bcr.09.2009.2234
PMID:22767658
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3029839/
Abstract

Essential thrombocythemia (ET) is a chronic myeloproliferative neoplasm which can cause thrombohaemorrhagic complications usually involving microvasculature. Medium-sized arterial thrombosis has been reported, but coronary occlusion usually occurs with additional risk factors, for example, smoking, hyperlipidaemia and so on. We present a case of acute myocardial infarction (AMI) in a young man (29 years) with ET but without any coronary artery associated risk factors. He was successfully treated for his AMI and ET with cytoreductive treatment and has recovered well. Due to automated platelet counting, ET is being increasingly identified; early detection can prevent long-term complications, and patients can have normal life span.

摘要

原发性血小板增多症(ET)是一种慢性骨髓增殖性肿瘤,可导致血栓出血并发症,通常累及微血管。有报道称发生了中等大小动脉血栓形成,但冠状动脉闭塞通常在存在其他危险因素(如吸烟、高脂血症等)时发生。我们报告一例29岁患有ET但无任何冠状动脉相关危险因素的青年男性急性心肌梗死(AMI)病例。他通过细胞减灭治疗成功治疗了AMI和ET,恢复良好。由于自动血小板计数,ET越来越多地被识别出来;早期检测可预防长期并发症,患者可拥有正常寿命。