Bansal Neha, Walters Henry L, Aggarwal Sanjeev
Division of Cardiology, 2969Children's Hospital of Michigan, Wayne State University School of Medicine, Detroit, MI, USA.
Division of Cardiothoracic Surgery, 2969Children's Hospital of Michigan, Detroit, MI, USA.
World J Pediatr Congenit Heart Surg. 2021 May;12(3):433-436. doi: 10.1177/2150135118824077. Epub 2019 May 14.
Cardiac paraganglioma (PGL) is a rare catecholamine-secreting tumor forming 1% to 3% of cardiac tumors. Although most PGL occur sporadically, evidence exists that 40% of them may be related to familial cancer predisposition syndromes. We present a unique case of a 14-year-old female who presented with persistent hypertension and was found to have a cardiac PGL. During surgical resection, even though the main right coronary was preserved, the sinoatrial (SA) nodal artery was surrounded by the tumor and required resection with the tumor. The patient subsequently developed SA node dysfunction and is currently being evaluated for placement of a permanent pacemaker.
心脏副神经节瘤(PGL)是一种罕见的分泌儿茶酚胺的肿瘤,占心脏肿瘤的1%至3%。尽管大多数PGL是散发性发生的,但有证据表明其中40%可能与家族性癌症易感综合征有关。我们报告了一例独特的病例,一名14岁女性因持续性高血压就诊,被发现患有心脏PGL。在手术切除过程中,尽管右冠状动脉主干得以保留,但窦房(SA)结动脉被肿瘤包绕,需要与肿瘤一并切除。患者随后出现窦房结功能障碍,目前正在评估是否需要植入永久性起搏器。