Pheochromocytoma: evaluation, diagnosis, and treatment

Citation
Mm. Walther et al., Pheochromocytoma: evaluation, diagnosis, and treatment, WORLD J URO, 17(1), 1999, pp. 35-39
Citations number
47
Categorie Soggetti
Urology & Nephrology
Journal title
WORLD JOURNAL OF UROLOGY
ISSN journal
07244983 → ACNP
Volume
17
Issue
1
Year of publication
1999
Pages
35 - 39
Database
ISI
SICI code
0724-4983(199902)17:1<35:PEDAT>2.0.ZU;2-Q
Abstract
Pheochromocytoma is a catecholamine-producing tumor of the sympathetic nerv ous system. Signs and symptoms are generally related to catecholamine exces s; these include hypertension, sweating, palpitatione, headaches, and anxie ty attacks. Abdominal imaging and 24-h urine collection for catecholamines are usually be sufficient for diagnosis. Catecholamine blockade with phenox ybenzamine and metyrosine generally ameliorates symptoms and is necessary t o prevent hypertensive crisis during surgery. Standard treatment is laparos copic adrenalectomy, although partial adrenalectomy is gaining enthusiastic support in familial forms of pheochromocytoma.