Velilla Marco J, Gonzalo Hernández C, Alonso Casas F, Gutiérrez Ganzaráin A I, Andrés Aguilar J L, Monzón Lomas F J
Servicio de Medicina Interna, Hospital Miguel Servet, Zaragoza.
An Med Interna. 1991 May;8(5):238-40.
Intrapericardial pheochromocytomas are extremely rare tumors. Diagnosing and localizing them are very difficult tasks when using conventional methods used for adrenal pheochromocytoma. We present the case of a patient with a pheochromocytoma who had a CT scan of the thorax and abdomen performed, as well as 131I methaiodinebencilguanidin (131 I-MIBG) gammagraphy, with completely normal results. The tumor was localized in the mediastinal area using 123 I-MIBG and NMR. The tumor was found intrapericardial during the operation; it was fixed to the pulmonary artery and in close contact with the left atrial, as well as with the circumflex and aorta arteries. It was possible to carry out the resection without causing any damage to these structures.
心包内嗜铬细胞瘤是极其罕见的肿瘤。使用用于肾上腺嗜铬细胞瘤的传统方法对其进行诊断和定位是非常困难的任务。我们报告了一例嗜铬细胞瘤患者的病例,该患者进行了胸部和腹部CT扫描以及131I间碘苄胍(131I-MIBG)闪烁扫描,结果完全正常。使用123I-MIBG和核磁共振成像(NMR)将肿瘤定位在纵隔区域。手术中发现肿瘤位于心包内;它附着于肺动脉,与左心房以及回旋支动脉和主动脉紧密相连。能够在不损伤这些结构的情况下进行切除。