A rare association between acromegaly and pheochromocytoma

Citation
J. Baughan et al., A rare association between acromegaly and pheochromocytoma, AM J SURG, 182(2), 2001, pp. 185-187
Citations number
10
Categorie Soggetti
Surgery,"Medical Research Diagnosis & Treatment
Journal title
AMERICAN JOURNAL OF SURGERY
ISSN journal
00029610 → ACNP
Volume
182
Issue
2
Year of publication
2001
Pages
185 - 187
Database
ISI
SICI code
0002-9610(200108)182:2<185:ARABAA>2.0.ZU;2-B
Abstract
The occurrence of multiple endocrine tumors is rare; however, they may be f ound with hereditary diseases such as multiple endocrine neoplasia (MEN). T he endocrine tumors involved with these diseases are well documented. We pr esent a case of a patient with a pheochromocytoma and a growth hormone (GH) secreting pituitary adenoma. This association is not described with any of the known MEN syndromes. The association may be a cross-over MEN syndrome or a secondarily induced GH-secreting pituitary adenoma from a pheochromocy toma producing growth hormone releasing hormone (GHRH) instead of catechola mines. (C) 2001 Excerpta Medica, Inc. All rights reserved.