Double-territory STEMI with Cardiogenic shock in ITP with severe Thrombocytopenia – A Case Report

Yerramareddy Vijayachandra, Antony Wilson, Jayalakshmi Sreeram, Aishwarya Mahesh Kumar
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Abstract

Myocardial infarction in a patient with immune thrombocytopenia is a rare scenario which is very challenging to manage. We present a rare case of a patient with immune thrombocytopenic purpura who developed double territory ST-elevation myocardial infarction with cardiogenic shock. She had an extremely rare presentation with a fresh mobile thrombus in the aortic root which was trap-dooring the right coronary artery ostium and extending into the artery with embolism into the distal left anterior descending artery. We managed this patient conservatively with excellent recovery owing to the dangerous location of the hanging thrombus, and severe thrombocytopenia. Multidisciplinary approach is required for the management of myocardial infarction in patients with pre-existing blood disorders, with therapy tailored to the patient's presentation and treatment requirements.
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严重血小板减少的 ITP 患者双发 STEMI 并发心源性休克 - 病例报告
免疫性血小板减少症患者发生心肌梗死是一种罕见的情况,处理起来非常具有挑战性。 我们介绍了一例罕见的免疫性血小板减少性紫癜患者,她发生了双区 ST 段抬高型心肌梗死并伴有心源性休克。她的表现极为罕见,主动脉根部有一个新鲜的移动血栓,血栓在右冠状动脉骨膜上形成陷阱,并延伸到动脉内,栓塞到左前降支动脉远端。由于悬吊血栓位置危险,且血小板严重减少,我们对该患者进行了保守治疗,患者恢复良好。 在治疗原有血液疾病患者的心肌梗死时,需要采取多学科方法,并根据患者的表现和治疗要求进行治疗。
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