| Literature DB >> 7435832 |
E Abemayor, A H Harken, C E Koop.
Abstract
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.Entities:
Mesh:
Year: 1980 PMID: 7435832 DOI: 10.1016/0002-9610(80)90061-6
Source DB: PubMed Journal: Am J Surg ISSN: 0002-9610 Impact factor: 2.565