ea0003p150 | Endocrine Tumours and Neoplasia | BES2002
Abraham P
, Watson W
, Park C
, Philip S
, Bandyopadhyay S
, Acharya S
, Talbot J
, White A
, Bevan J
Phaeochromocytoma in association with hypercortisolism is thought to be rare. However we have observed 4 cases in 3 years and question the rarity of this link. In each case there was a dominant adrenal mass (3.6-7.7cm) with contralateral adrenal hyperplasia. Three of the 4 tumours showed increased 123-I-mIBG uptake. Urinary catecholamines ranged from 872-22752nmol/24h (N < 600). Hypercortisolism was present in all 4 patients; sustained in 2 and cyclical in 2. Case 1 (JCEM ...