Searchable abstracts of presentations at key conferences in endocrinology

ea0011p84 | Clinical case reports | ECE2006

Hypopituitarism in an adult thalassemic patient. Effects of different replacement therapies

Danesi L , Cattaneo A , Lavezzi E , Scacchi M , Cavagnini F

In a small but not negligible proportion of thalassemic patients, a true growth hormone deficiency (GHD), not secondary to pubertal delay, can be documented. Among the features of adult GHD syndrome, osteoporosis leads to a 2.5-fold increase in fracture risk. Thalassemia is characterized by a peculiar bone disease leading to osteopenia. The effectiveness of GH treatment in GHD adult thalassemic patients has not been explored yet. We report here the case of such a patient, disp...

ea0011p493 | Endocrine tumours and neoplasia | ECE2006

Carney’s complex with acromegaly as the leading clinical condition

Fatti LM , Bertola G , Balza G , Lavezzi E , Pecori Giraldi F , Cavagnini F

Carney’s complex was first identified as the association of primary adrenal nodular dysplasia, lentigines and cardiac and skin myxomas. Several other endocrine and non-endocrine disorders were subsequently added to the complex, including pituitary tumors and melanotic Schwannomas. We herewith describe a kindred with Carney’s complex featuring acromegaly as the common denominator.Patients & methods: A 42-year-old woman first presented to our...