Farias Francisco, Yogeswaran Vidhushei, Hidano Danelle, Starnes Elizabeth, Kwon Young, Branch Kelley, Tylee Tracy, Poole Jeanne, Sridhar Arun
Department of Medicine, University of Washington, Seattle, WA, USA.
Division of Cardiology, Department of Medicine, University of Washington, Seattle, WA, USA.
J Cardiol Cases. 2023 Mar 25;27(5):222-225. doi: 10.1016/j.jccase.2023.02.011. eCollection 2023 May.
Pheochromocytomas are catecholamine-producing tumors and a rare cause of sudden cardiac death. We describe the case of a previously healthy 28-year-old man who presented after a ventricular fibrillation out-of-hospital cardiac arrest (OHCA). His clinical investigation, including a coronary evaluation, was unremarkable. A protocolized head-to-pelvis computed tomography (CT) scan was ordered and revealed a large right adrenal mass with subsequent laboratory studies showing markedly elevated urine and plasma catecholamines. This raised suspicion for a pheochromocytoma as the underlying etiology behind his OHCA. He received appropriate medical management, underwent adrenalectomy with subsequent normalization of his metanephrines, and fortunately did not have recurrent arrythmias. This case highlights the first documented case of a ventricular fibrillation arrest as the initial presentation of pheochromocytoma crisis in a previously healthy individual, and how the use of early protocolized sudden death CT scan allowed for the prompt diagnosis and management of a rare cause of OHCA.
We review the typical cardiac manifestations of pheochromocytoma and describe the first case of a pheochromocytoma crisis presenting as sudden cardiac death (SCD) in a previously asymptomatic individual. In young patients with unexplained SCD, it is important to consider pheochromocytoma in the differential diagnosis. We also review why an early head-to-pelvis sudden death computed tomography scan protocol may be helpful in the evaluation of patients resuscitated from SCD without an obvious etiology.
嗜铬细胞瘤是分泌儿茶酚胺的肿瘤,是心源性猝死的罕见原因。我们描述了一名28岁既往健康男性的病例,他在院外心脏骤停(OHCA)后发生心室颤动后就诊。他的临床检查,包括冠状动脉评估,均无异常。随后进行了一项从头部到骨盆的标准化计算机断层扫描(CT),发现右侧肾上腺有一个大肿块,随后的实验室检查显示尿和血浆儿茶酚胺明显升高。这引发了对嗜铬细胞瘤作为其OHCA潜在病因的怀疑。他接受了适当的医疗管理,接受了肾上腺切除术,随后甲氧基肾上腺素恢复正常,幸运的是没有再次出现心律失常。该病例突出了首次记录的一例心室颤动骤停作为嗜铬细胞瘤危象在既往健康个体中的初始表现,以及早期标准化猝死CT扫描的应用如何能够迅速诊断和处理OHCA的罕见病因。
我们回顾了嗜铬细胞瘤的典型心脏表现,并描述了首例嗜铬细胞瘤危象在既往无症状个体中表现为心源性猝死(SCD)的病例。在不明原因SCD的年轻患者中,在鉴别诊断时考虑嗜铬细胞瘤很重要。我们还回顾了为什么早期从头部到骨盆的猝死计算机断层扫描方案可能有助于评估从无明显病因的SCD中复苏的患者。