Grissom J R, Yamase H T, Prosser P R
South Med J. 1979 Dec;72(12):1605-7. doi: 10.1097/00007611-197912000-00035.
We describe a case of an asymptomatic patient with a huge left abdominal mass, which at operation was found to be a cystic pheochromocytoma weighing over 3,000 gm. A dignosis of sarcoidosis was established simultaneously, with the discovery of sarcoid granulomas in abdominal nodes and within the tumor mass itself. This is only the second observation of coexistent sarcoidosis and pheochromocytoma, and with the paucity of related literature, we conclude the association is probably fortuitous.
我们描述了一例无症状患者，其左腹部有一巨大肿块，手术时发现是一个重达3000多克的囊性嗜铬细胞瘤。同时，通过在腹部淋巴结及肿瘤块本身发现结节病肉芽肿，确诊为结节病。这是共存结节病和嗜铬细胞瘤的第二例观察报道，鉴于相关文献较少，我们得出这种关联可能是偶然的结论。
