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室性心动过速的罕见病因:嗜铬细胞瘤。

Rare cause of ventricular tachycardia: Pheochromocytoma.

作者信息

Delekta Joanna, Riahi Sam, Eschen Ole

机构信息

Department of Cardiology, Aalborg University Hospital, Hobrovej 18-22, 9000 Aalborg, Denmark.

出版信息

J Cardiol Cases. 2014 Nov 14;11(2):62-65. doi: 10.1016/j.jccase.2014.10.007. eCollection 2015 Feb.

Abstract

Pheochromocytoma is known from a wide range of clinical manifestations and can mimic other disorders which can lead to delay in diagnosis. We report a case of a young female presenting with chest pain, electrocardiographic changes, and episodes of ventricular tachycardia, finally diagnosed with this catecholamine-producing tumor. < Pheochromocytoma is a rare catecholamine-producing tumor that can pose a diagnostic challenge due to its multiple manifestations mimicking various conditions, including cardiovascular disorders. Despite its infrequent occurrence, pheochromocytoma should be considered as a possible cause of life-threatening cardiac arrhythmias and electrocardiographic changes in patients with diagnostic difficulties and primarily suspected of having cardiovascular disease. Furthermore, the method of treatment is entirely different.>.

摘要

嗜铬细胞瘤有多种临床表现,可酷似其他疾病,从而导致诊断延误。我们报告一例年轻女性病例,该患者表现为胸痛、心电图改变及室性心动过速发作,最终诊断为这种分泌儿茶酚胺的肿瘤。<嗜铬细胞瘤是一种罕见的分泌儿茶酚胺的肿瘤,因其多种表现可酷似包括心血管疾病在内的各种情况,故可带来诊断挑战。尽管其发病率低,但对于诊断困难且主要怀疑患有心血管疾病的患者,嗜铬细胞瘤应被视为危及生命的心律失常和心电图改变的可能病因。此外,其治疗方法完全不同。>

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Rare cause of ventricular tachycardia: Pheochromocytoma.室性心动过速的罕见病因:嗜铬细胞瘤。
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Cardiovascular complications in patients with pheochromocytoma: a mini-review.嗜铬细胞瘤患者的心血管并发症:小型综述。
Biomed Pharmacother. 2010 Sep;64(7):505-9. doi: 10.1016/j.biopha.2009.09.014. Epub 2009 Nov 17.
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Life-threatening cardiac manifestations of pheochromocytoma.嗜铬细胞瘤危及生命的心脏表现。
Case Rep Med. 2010;2010:976120. doi: 10.1155/2010/976120. Epub 2010 Feb 10.
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QT prolongation and monomorphic VT caused by pheochromocytoma.QT 延长和嗜铬细胞瘤引起的单形性 VT。
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