Searchable abstracts of presentations at key conferences in endocrinology

ea0029p379 | Clinical case reports - Pituitary/Adrenal | ICEECE2012

Acromegaly, primary hyperparathyroidism and renal cell carcinoma

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...