Fadah Kahtan, Khalafi Seyed, Panneerselvam Ezhil, Lopes Jan, Abolbashari Mehran, Borges Jorge Chiquie, Okajima Kazue
Department of Internal Medicine, Texas Tech University Health Sciences Center, El Paso, TX, USA.
Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, TX, USA.
J Med Cases. 2025 Feb;16(2):55-60. doi: 10.14740/jmc5096. Epub 2025 Jan 17.
Intramyocardial dissecting hematoma (IDH) is a rare complication that may emerge from myocardial infarction, thoracic injury, or percutaneous intervention. In the past, IDH was diagnosed through surgical intervention or postmortem autopsy. We present a case of a 70-year-old male with comorbidities who admitted to the intensive care unit after suffering out of hospital pulseless electrical activity cardiac arrest and obtained return of spontaneous circulation after chest compressions. Initial electrocardiogram (ECG) showed ST elevation in the anterolateral leads. Repeated ECG a few minutes later showed junctional rhythm bradycardia with a rate of 27 and serial changes of an anterolateral infarct were present and placed on percutaneous pacing with vasopressors. The troponin I peaked at 1.880. Transthoracic echocardiography (TTE) portrayed a hyperechoic mobile filamentous structure near the cardiac apex, which was thought to be a false left ventricular (LV) tendon initially. A repeat TTE with the use of an ultrasound enhancing agent (sulfur hexafluoride) revealed an apical neocavity with no contrast filling, suggestive of a large apical IDH within the LV. The patient expired because of cardiac arrest secondary to cardiogenic shock refractory to pressor support, with no autopsy performed. This case highlights an uncommon and timelier diagnostic modality of IDH in deference of more costly and prolonged imaging studies.
心肌内夹层血肿(IDH)是一种罕见的并发症,可能源于心肌梗死、胸部损伤或经皮介入治疗。过去,IDH通过手术干预或尸检诊断。我们报告一例70岁男性合并症患者,在院外发生无脉电活动心脏骤停后入住重症监护病房,经胸外按压后恢复自主循环。初始心电图(ECG)显示前侧壁导联ST段抬高。几分钟后的重复心电图显示交界性心律心动过缓,心率为27次/分,存在前侧壁梗死的系列变化,并接受了经皮起搏及血管加压药治疗。肌钙蛋白I峰值为1.880。经胸超声心动图(TTE)显示心尖附近有一个高回声可移动丝状结构,最初被认为是左心室(LV)假腱。使用超声增强剂(六氟化硫)进行的重复TTE显示心尖部有一个新腔,无造影剂填充,提示LV内有一个巨大的心尖部IDH。患者因对升压药支持无效的心源性休克继发心脏骤停死亡,未进行尸检。本病例强调了一种罕见且及时的IDH诊断方式,避免了更昂贵和耗时的影像学检查。