Lin J C, Palafox B A, Jackson H A, Cohen A J, Gazzaniga A B
Department of Surgery, Children's Hospital of Orange County, Orange, California, USA.
Ann Thorac Surg. 1999 Feb;67(2):555-8. doi: 10.1016/s0003-4975(98)01291-0.
Cardiac pheochromocytoma is an exceedingly rare and unusual clinical entity. Only 37 previous surgically treated adult patients were found in review of the surgical literature. We report the case of a 13-year-old boy who had a cardiac pheochromocytoma that was localized by the 111-indium diethylenetriamine pentaacetic acid octreotide scintigraphy scan and confirmed by magnetic resonance imaging after computed tomographic and B1-iodine-metaiodobenzylguanidine scans had failed. At operation, a 6-cm pheochromocytoma of the left atrium was found and successfully resected with reconstruction of the left atrium using autologous pericardium.
心脏嗜铬细胞瘤是一种极其罕见且特殊的临床病症。回顾外科文献发现,之前仅有37例接受手术治疗的成年患者。我们报告一例13岁男孩的病例,其心脏嗜铬细胞瘤通过铟-111二乙三胺五乙酸奥曲肽闪烁扫描定位,在计算机断层扫描和碘-131间碘苄胍扫描失败后,经磁共振成像得以确诊。手术中,发现左心房有一个6厘米的嗜铬细胞瘤,并成功切除,同时使用自体心包对左心房进行了重建。