一名 7 个月大患有家族性嗜血细胞淋巴组织细胞增多症的婴儿患上了塔克次氏心肌病:病例报告

Payal Gupta, S. S. Patil, U. Pillay
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引用次数: 0

摘要

塔克次氏心肌病是一种急性心脏疾病,在没有冠状动脉疾病的情况下可模拟急性心肌梗死。我们介绍了一例 7 个月大的女孩的病例,她因潜在的家族性嗜血细胞淋巴组织细胞增多症导致临床症状恶化而住进一家三级医院的儿科重症监护室(PICU)。在 PICU 留院期间,超声心动图检查发现患者心脏收缩力严重受损,左心室出现特征性的区域室壁运动异常。再加上心肌酶升高,患者被诊断为塔库洼心肌病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Takotsubo cardiomyopathy in a 7-month-old infant with familial hemophagocytic lymphohistiocytosis: A case report
Takotsubo cardiomyopathy constitutes an acute cardiac condition that mimics acute myocardial infarction in the absence of coronary artery disease. We present a case of a 7-month-old girl, who was admitted in the pediatric intensive care unit (PICU) at a tertiary care hospital for clinical deterioration with underlying familial hemophagocytic lymphohistiocytosis. During the PICU stay, on echocardiography, the patient had severe cardiac contractility compromise with a characteristic pattern of regional wall motion abnormalities of the left ventricle. This, in combination with elevated cardiac enzymes, led to the diagnosis of takotsubo cardiomyopathy.
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