Leite Luiz R, Macedo Paula G, Santos Simone N, Quaglia Luiz, Mesas Cezar E, De Paola Angelo
Department of Clinical Cardiac Electrophysiology, Centro de Estudos em Arritmia Cardíaca, SMDB Conj. 16 Lote 5 Cs A, Brasilia-DF 71680-160, Brazil.
Case Rep Med. 2010;2010:976120. doi: 10.1155/2010/976120. Epub 2010 Feb 10.
Pheochromocytoma is a catecholamine-secreting tumor of the adrenal glands, usually with benign manifestations, whose typical clinical presentation includes the triad of headache, palpitations and diaphoresis. However, a wide range of signs and symptoms may be present. In the cardiovascular system, the most common signs are labile hypertension and sinus tachycardia. Systolic heart failure and ST-segment deviations mimicking myocardial infarction have also been reported, as well as QT interval prolongation and, rarely, ventricular tachycardia. We describe a challenging diagnosis of pheochromocytoma with many cardiovascular manifestations, which could have been missed due to the absence of typical symptoms.
嗜铬细胞瘤是一种分泌儿茶酚胺的肾上腺肿瘤,通常表现为良性,其典型临床表现包括头痛、心悸和多汗三联征。然而,可能会出现广泛的体征和症状。在心血管系统中,最常见的体征是血压波动和窦性心动过速。也有报告称出现收缩性心力衰竭和类似心肌梗死的ST段偏移,以及QT间期延长,很少见的还有室性心动过速。我们描述了一例具有许多心血管表现的嗜铬细胞瘤的挑战性诊断,由于缺乏典型症状,该病例可能被漏诊。