法洛四联症合并嗜铬细胞瘤：一项不同寻常的治疗挑战。
Tetralogy of Fallot with pheochromocytoma: an unusual therapeutic challenge.
作者信息
Balakrishnan Gautam, Ravikumar Ratnagiri, Rao Suresh, Balakrishnan Komarakshi R
机构信息
Department of Internal Medicine, Fortis Malar Hospital, Chennai, India.
出版信息
Asian Cardiovasc Thorac Ann. 2013 Aug;21(4):464-6. doi: 10.1177/0218492312456979. Epub 2013 Jul 1.
An adult with unoperated tetralogy of Fallot diagnosed simultaneously with pheochromocytoma is extremely rare. This poses obvious diagnostic and therapeutic challenges. A 29-year-old woman with these conditions was successfully operated on for both diseases in the same hospitalization. There is some interesting speculation regarding the association of pheochromocytoma with uncorrected cyanotic congenital heart disease.
一名成年法洛四联症未手术患者同时被诊断出患有嗜铬细胞瘤，这种情况极为罕见。这带来了明显的诊断和治疗挑战。一名患有这两种疾病的29岁女性在同一次住院期间成功接受了针对这两种疾病的手术。关于嗜铬细胞瘤与未经矫正的青紫型先天性心脏病之间的关联，存在一些有趣的推测。
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