ST elevation myocardial infarction as presenting feature of acute myeloid leukemia

K.V. Harish , Revanth Boddu , Kundan Mishra , Kanwaljeet Singh , S.K. Pramanik
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Abstract

A 35-year-old male patient with acute myeloid leukemia (AML), with hyperleukocytosis, presented with acute myocardial infarction. The individual had acute onset chest pain and reached the hospital within the window period. His electrocardiogram (ECG) revealed ST elevated myocardial infarction (STEMI), ST elevated myocardial infarction, and thrombolysis was performed. Postthrombolysis, there was no resolution of ST elevation, and coronary angiography revealed normal coronaries. His blood picture showed hyperleukocytosis with 80% blasts, and bone marrow and flow cytometry confirmed the diagnosis of AML. Considering the central role of white blood cell in the remodeling of myocardial tissue, it was obvious that administration of chemotherapy with its inevitable pancytopenia could impose an increased risk for further cardiac complications. Nevertheless, cytarabine-based induction chemotherapy was initiated; on the third day, he developed bilateral diffuse alveolar hemorrhage. He was managed with mechanical ventilation, component support, empirical antibiotics, and other bundled care. The patient died 2 days later with diffuse alveolar hemorrhage and leukemia.
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ST段抬高型心肌梗死是急性髓性白血病的表现特征
一例35岁男性急性髓性白血病(AML)患者,伴白细胞增多症,表现为急性心肌梗死。该患者有急性胸痛,并在窗口期到达医院。心电图显示ST段抬高型心肌梗死(STEMI), ST段抬高型心肌梗死,行溶栓治疗。溶栓后,ST段抬高未见缓解,冠状动脉造影显示冠状动脉正常。他的血液图像显示白细胞增多,80%为原细胞,骨髓和流式细胞术证实了AML的诊断。考虑到白细胞在心肌组织重塑中的核心作用,很明显,化疗不可避免地会导致全血细胞减少,这可能会增加进一步心脏并发症的风险。然而,还是开始了以阿糖胞苷为基础的诱导化疗;第3天出现双侧弥漫性肺泡出血。他接受了机械通气、部件支持、经验性抗生素和其他捆绑护理。患者2天后死于弥漫性肺泡出血和白血病。
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来源期刊
Medical Journal Armed Forces India
Medical Journal Armed Forces India Medicine-Medicine (all)
CiteScore
3.40
自引率
0.00%
发文量
206
期刊介绍: This journal was conceived in 1945 as the Journal of Indian Army Medical Corps. Col DR Thapar was the first Editor who published it on behalf of Lt. Gen Gordon Wilson, the then Director of Medical Services in India. Over the years the journal has achieved various milestones. Presently it is published in Vancouver style, printed on offset, and has a distribution exceeding 5000 per issue. It is published in January, April, July and October each year.
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