Searchable abstracts of presentations at key conferences in endocrinology

ea0011p89 | Clinical case reports | ECE2006

A case of adult GH deficit in a woman with Autoimmune Polyendocrine Syndrome type II

Pietrobono D , Bassotti G , Diacono F , Iuorio R , Mercuri V , Gargiulo P

We report a case of a 53 years old woman who presented asthenia, cramps, cutaneous hyperpigmentation, nausea, vomiting, vague and non-specific epigastric abdominal pain, weight loss and hypotension. She was diagnosed with Addison’s disease because biochemical data were indicative for autoimmune adrenal failure (positivity for adrenal cortex antibodies). Nevertheless during the following 9 years the patient began to note the progressive reduction of pubic and axillary hair...

ea0011p459 | Endocrine tumours and neoplasia | ECE2006

Role of family history for diabetes mellitus in determining insulin resistance in acromegalic patients

Diacono F , Pietrobono D , Bassotti G , Borgognoni L , Di Sarra D , Iuorio R , Gargiulo P , Tamburrano G

Objective: Acromegaly is a rare pituitary disease due to excessive secretion of GH. Insulin resistance, impaired glucose tolerance (IGT) and diabetes mellitus (DM) are common features in acromegaly. Seventy-four active acromegalic patients were retrospectively evaluated in order to determine the impact of family history for diabetes mellitus on glucose tolerance, insulin resistance and beta-cell function.Patients and methods: We studied 74 patients with ...