Searchable abstracts of presentations at key conferences in endocrinology

ea0063p736 | Pituitary and Neuroendocrinology 2 | ECE2019

Prevalence of silent acromegaly in prolactinomas (PASP): an Italian experience

Bona Chiara , Prencipe Nunzia , Mantonavi Giovanna , Lanzi Roberto , Jaffrain-Rea Marie-Lise , Ambrosio Maria Rosaria , Pasquali Daniela , Vettor Roberto , Cannavo Salvatore , Ghigo Ezio , Grottoli Silvia

Patients with prolactinomas may develop acromegaly during D2-agonists (DA), suggesting the existence of somatomammotroph adenomas with asynchronous secretion of GH and PRL. This may be due to the acquisition of somatotroph characteristics by lactotroph cells or to GH co-secretion by somatommammotroph cells unmasked after PRL inhibition by DA. The prevalence of silent acromegaly in prolactinomas during DA is 4.1%. The purpose of this study was to evaluate the somatotroph axis i...

ea0099rc2.4 | Rapid Communications 2: Calcium and Bone | Part I | ECE2024

Primary hyperparathyroidism in children and adolescents: Clinical features and treatment outcomes from an Italian multicenter study

Cetani Filomena , Della Valentina Simone , Scillitani Alfredo , Dal Lago Anna , Pierotti Laura , Sardella Chiara , Madeo Bruno , Cairoli Elisa , Eller Vainicher Cristina , Procopio Massimo , Barale Marco , Palmieri Serena , Gianotti Laura , Castellano Elena , Lania Andrea , Pitea Marco , Lanzi Roberto , Maggiore Riccardo , Cipriani Cristiana , Pepe Jessica , Corbetta Sabrina

Primary hyperparathyroidism (PHPT) is rare in the pediatric population, with an estimated incidence of 0.5–5 cases per 100,000 person-years in children. Data regarding the clinical phenotype, the surgical outcomes are scarce. The objective of our study was to retrospectively analyze the phenotype of apparently sporadic PHPT in patients ≤21 years in major endocrinology reference centers in Italy. None of the patients had known familial syndromes. A total of 41 patien...