Paraganglioma como causa de taquicardia ventricular maligna en un varón de 69 años

Lucía Torres-Quintero , Daniel Castro-Fernández , Luis Tercedor Sánchez
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Abstract

Pheochromocytomas and paragangliomas are catecholamine-secreting neuroendocrine tumors. Resecting a pheochromocytoma or paraganglioma is a high-risk surgical procedure due to lethal hypertensive crises, malignant arrhythmias, and multiorgan failure, requiring prior pharmacological preparation.

Below, we present the case of a 69-year-old man who underwent surgery whilst the presence of a paraganglioma was overlooked thus suffering ventricular tachycardia and hypertensive crises during the intervention and the postoperative period.

69岁男性恶性室性心动过速的原因
嗜铬细胞瘤和副神经节瘤是分泌儿茶酚胺的神经内分泌肿瘤。切除嗜铬细胞瘤或副神经节瘤是一种高风险的手术,由于致命的高血压危象、恶性心律失常和多器官衰竭,需要事先做好药理准备。下面,我们报告一名69岁的男性接受手术,而副神经节瘤的存在被忽视,因此在干预和术后期间遭受室性心动过速和高血压危象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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