Abemayor E, Harken A H, Koop C E
Am J Surg. 1980 Nov;140(5):696-7. doi: 10.1016/0002-9610(80)90061-6.
Pheochromocytoma is not rare; indeed, it was discovered in 0.1 percent of consecutive autopsies and in 0.64 percent of a large group of patients screened for hypertension. A patient who underwent excision of a pheochromocytoma at age 7 years is presented. Seven years later, bilateral metastatic pulmonary nodules were excised. Fourteen years later, two metastatic pulmonary nodules were again excised. The patient is doing well 1 year after discharge. Surgical resection of multiple metastatic pheochromocytoma nodules is recommended.
嗜铬细胞瘤并不罕见;事实上,在连续尸检的0.1%中以及在一大群接受高血压筛查的患者的0.64%中被发现。本文报告一名7岁时接受嗜铬细胞瘤切除术的患者。7年后,切除双侧转移性肺结节。14年后,再次切除两个转移性肺结节。患者出院1年后情况良好。建议对多发性转移性嗜铬细胞瘤结节进行手术切除。