ea0029p379 | Clinical case reports - Pituitary/Adrenal | ICEECE2012
Nogueira C.
, Vinha E.
, Mesquita J.
, Belo S.
, Capela J.
, Pereira J.
, Coutinho H.
, Castro L.
, Souto-Moura C.
, Resende A.
, Bernardes I.
, Carvalho D.
Introduction: Acromegaly is a rare disorder and sporadic cases are the most frequent. It can also occur in association with genetic syndromes, such as Carney complex, multiple endocrine neoplasia type 1 (MEN-1), MEN-1 like syndrome, isolated familial acromegaly and familial isolated pituitary adenomas.Case report: Thirty five -year-old man was observed in 1994 for gynecomastia. Acromegaly was diagnosed based on clinical, biochemical (IGF1 1094.7 ng/ml, b...