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Serious takotsubo cardiomyopathy: an autopsy case presenting severe irreversible myocardial damage after frequent episodes of recurrence

机译:严重的takotsubo心肌病:尸检案例在经常发作后呈现严重的不可逆心肌损伤

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BACKGROUND:Takotsubo cardiomyopathy is characterized by transient dysfunction of the medial to apical segment of the left ventricle. Recurrence within a few months or years has been reported and serious complications, including arrhythmia, acute cardiac shock and cardiac rupture, can arise; however, recurrence is rare and takotsubo cardiomyopathy is typically a reversible functional disorder.CASE PRESENTATION:A 91-year-old Japanese woman with a past medical history of angina pectoris, hypertension and uterine carcinoma noted bilateral axillary pain and presented herself to an emergency room. Although the pain improved and she went home, there were several subsequent episodes of recurrent chest pain. At approximately 1 week after the onset, she was hospitalized as her symptom worsened. Electrocardiography showed low voltage in limb and chest leads, and ST-segment elevation in leads II, III, aVF and V3 to V6. Echocardiography revealed medial to apical dyskinesia and basal hypercontractility of the left ventricle, and cardiac tamponade. Pericardiocentesis improved the symptom, but not her cardiac dysfunction. At 3 days after her admission, cardiopulmonary resuscitation was performed due to ventricular fibrillation. She died on the 5th day of admission (2 weeks after the onset). At autopsy, the left ventricle was dilatated and the apical ventricular wall was thin. On microscopy, remarkable wavy change and thinning of myocardium were diffusely observed, especially at the apex and the anterior to lateral wall of the left ventricle, interventricular septum and right ventricle, intermingled with interstitial fibrosis, hemorrhage and neutrophil infiltration. Contraction band necrosis was mainly observed on the posterior to inferior wall of the left ventricle.CONCLUSION:Our case showed severe morphological myocardial change after several chest pain episodes that were considered to be takotsubo cardiomyopathy. This notable case suggests that the frequent recurrence of serious takotsubo cardiomyopathy is life threatening and can lead to irreversible serious myocardial degeneration.
机译:背景:Takotsubo心肌病的特征在于左心室内侧瞬态功能障碍。几个月或几年内的复发已经报告,并且可能出现严重并发症,包括心律失常,急性心脏休克和心脏破裂;然而,复发是罕见的,Takotsubo心肌病通常是可逆的功能性障碍.Case演示:一个91岁的日本女性,具有过去的心绞痛病史,高血压和子宫癌的双侧腋窝疼痛,并给予急诊室。虽然疼痛改善了,但她回家了,但随后有几集的复发性胸痛。在发病后大约1周,她住院,因为她的症状恶化了。心电图显示肢体和胸部引线的低电压,以及引线II,III,AVF和V3至V6的ST段升高。超声心动图揭示了左心室的顶端性障碍和基础腹膜障碍和心脏铺位的基础滞后性。心包穿刺术改善了症状,但不是她的心脏功能障碍。在她入院后3天,由于心室颤动而进行了心肺重新刺除。她在入院的第5天(发病后2周)去世了。在尸检时,左心室膨胀,顶壁壁薄。在显微镜下,显着的波动变化和心肌的变薄被扩散,特别是在顶点和左侧壁的侧壁,间隔内隔和右心室的侧壁上,涉及间隙纤维化,出血和中性粒细胞渗透。在左心室的后壁后面主要观察到收缩带坏死。结论:我们的病例显示出几次胸痛发作后的严重形态心肌变化,被认为是Takotsubo心肌病。这一值得注意的情况表明,严重的Takotsubo心肌病的频繁复发是危及生命,可以导致不可逆的严重心肌变性。

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