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一名12岁男孩因急性脑干出血引发的应激性心肌病——病例报告

Takotsubo cardiomyopathy in a 12-year-old boy caused by acute brainstem bleeding-a case report.

作者信息

Thomas Clara, Johler Sarah M, Hermann Matthias, Fischer Marcus, Thorsteinsdottir Jun, Schichor Christian, Haas Nikolaus A

机构信息

Department for Pediatric Cardiology and Intensive Care, Medical Hospital of the University of Munich, Ludwig Maximilians University Munich, Munich, Germany.

Department for Neurosurgery, Medical Hospital of the University of Munich, Ludwig Maximilians University Munich, Munich, Germany.

出版信息

Transl Pediatr. 2021 Nov;10(11):3110-3117. doi: 10.21037/tp-21-181.

Abstract

Takotsubo cardiomyopathy is characterized by acute and reversible severe left ventricular dysfunction due to intensive emotional or physical stress followed by catecholamine excess. Traditionally it is most common in postmenopausal women, whereas only few cases have been described in childhood. In our case a previously well 12-year-old boy presented with severe cardiogenic shock due to dramatically impaired left ventricular function requiring significant inotropic support and invasive mechanical ventilation. Interestingly, cardiac catheterization, myocardial tissue histology and biochemical laboratory tests did not yield a definitive diagnosis. As his cardiac function improved gradually within several days and deep sedation could be weaned, he was then found to suffer from hemiparesis and absence of protective airway reflexes on neurological examination during the weaning process. Subsequent brain imaging studies revealed a brainstem bleeding due to a fistulous arteriovenous malformation (AVM) appearing to be only a few days old. After endovascular coiling and subsequent microsurgical resection of the malformation, he recovered completely. Our present case demonstrated, that brainstem bleeding could precipitate Takotsubo cardiomyopathy manifesting hemodynamic collapse. Severe ventricular impairment has been described in many adults with subarachnoid hemorrhage; however, this condition is extremely rare among children. When severe cardiogenic shock is diagnosed, precipitating factors such as intracranial processes should be ruled out on a regular basis.

摘要

应激性心肌病的特征是由于强烈的情绪或身体应激后儿茶酚胺过量导致急性且可逆的严重左心室功能障碍。传统上,该病在绝经后女性中最为常见,而儿童病例仅有少数报道。在我们的病例中,一名此前健康的12岁男孩因左心室功能严重受损出现严重的心源性休克,需要大量的正性肌力支持和有创机械通气。有趣的是,心脏导管检查、心肌组织学检查和生化实验室检查均未得出明确诊断。随着他的心脏功能在数天内逐渐改善且深度镇静可以撤机,在撤机过程中进行神经学检查时发现他患有偏瘫且气道保护性反射消失。随后的脑部影像学研究显示,由于一个似乎仅形成几天的瘘管型动静脉畸形(AVM)导致脑干出血。在对畸形进行血管内栓塞和随后的显微手术切除后,他完全康复。我们目前的病例表明,脑干出血可诱发表现为血流动力学崩溃的应激性心肌病。许多成人蛛网膜下腔出血患者中曾有严重心室功能损害的描述;然而,这种情况在儿童中极为罕见。当诊断出严重的心源性休克时,应定期排除诸如颅内病变等诱发因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36c2/8649596/032b9eb52470/tp-10-11-3110-f1.jpg

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