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[心肌病:嗜铬细胞瘤的首发临床表现——病例报告]

[Cardiomyopathy: first clinical manifestation of a pheochromocytoma--case report].

作者信息

Lopes Artur, Sousa Catarina, Correia Maria José, Júnior Correia, Rocha José, Pinto Fausto

机构信息

Serviço de Cardiologia, Hospital Divino Espírito Santo, Ponta Delgada, Portugal.

出版信息

Rev Port Cardiol. 2010 Jun;29(6):1065-9.

PMID:20967964
Abstract

Stress cardiomyopathy clinical presentation mimics an acute coronary syndrome. It is characterized by left ventricular multi-segmental commitment, absence of significant coronary artery disease and by the complete resolution of all the findings. Its pathophysiology is not yet clear, but the main theory suggests a catecholamine-mediated cardiotoxicity mechanism. Pheochromocytoma is a neuroendocrine tumor producer of catecholamines with several cardiovascular manifestations. We report a case of stress cardiomyopathy that was the first clinical manifestation of an unknown pheochromocytoma.

摘要

应激性心肌病的临床表现类似于急性冠状动脉综合征。其特征为左心室多节段受累、无明显冠状动脉疾病且所有表现均可完全缓解。其病理生理学尚不清楚,但主要理论认为是一种儿茶酚胺介导的心脏毒性机制。嗜铬细胞瘤是一种产生儿茶酚胺的神经内分泌肿瘤,有多种心血管表现。我们报告一例应激性心肌病病例,它是一例未知嗜铬细胞瘤的首发临床表现。

相似文献

1
[Cardiomyopathy: first clinical manifestation of a pheochromocytoma--case report].[心肌病:嗜铬细胞瘤的首发临床表现——病例报告]
Rev Port Cardiol. 2010 Jun;29(6):1065-9.
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Pheochromocytoma-induced ventricular tachycardia and reversible cardiomyopathy.嗜铬细胞瘤诱导的室性心动过速和可逆性心肌病。
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Sepsis and cardiomyopathy as rare clinical manifestations of pheochromocytoma--two case report studies.脓毒症和心肌病作为嗜铬细胞瘤的罕见临床表现——两项病例报告研究
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A rare cause of cardiogenic shock: catecholamine cardiomyopathy of pheochromocytoma.心源性休克的一种罕见病因:嗜铬细胞瘤所致儿茶酚胺心肌病。
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[Uncommon cardiac manifestations disclosing pheochromocytoma. Apropos of 3 cases].[揭示嗜铬细胞瘤的罕见心脏表现。附3例报告]
Ann Cardiol Angeiol (Paris). 1994 Jun;43(6):331-4.
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Cardiogenic shock with basal transient left ventricular ballooning (Takotsubo-like cardiomyopathy) as first presentation of pheochromocytoma.以基底节短暂性左心室球囊样变(Takotsubo 样心肌病)为首发表现的心原性休克合并嗜铬细胞瘤。
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A case of pheochromocytoma combined with catecholamine cardiomyopathy.
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Pheochromocytoma-Induced Cardiomyopathy Mimicking Acute Coronary Syndrome.嗜铬细胞瘤诱发的心肌病酷似急性冠状动脉综合征。
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引用本文的文献

1
"Never Trust to General Impressions, My Boy, but Concentrate Yourself upon Details": An Unusual and Challenging Presentation of Pheochromocytoma.“孩子,永远不要轻信总体印象,而要专注于细节”:嗜铬细胞瘤的一种不寻常且具有挑战性的表现
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