Searchable abstracts of presentations at key conferences in endocrinology

ea0099rc10.1 | Rapid Communications 10: Calcium and Bone | Part II | ECE2024

First-line F18-choline PET/CT Versus Tc99m-sestaMIBI SPECT/CT in the surgical management of primary hyperparathyroidism: a diagnostic randomized phase III trial

Quak Elske , Lasne-Cardon Audrey , Cavarec Marie-Beatrice , Lireux Barbara , Bastit Vianney , Roudaut Nathalie , Salaun Pierre-Yves , Keromnes Nathalie , Potard Gael , Vaduva Patricia , Esvant Annabelle , Jegoux Franck , De Crouy-Chanel Olivier , Devillers Anne , Guery Clemence , Christy Francois , Grellard Jean-Michel , Bardet Stephane , Clarisse Benedicte

Introduction: Whether F18-choline PET/CT (FCH PET/CT) should replace Tc99m-sestaMIBI SPECT/CT (MIBI SPECT/CT) as a first-line imaging technique for preoperative localisation of parathyroid adenomas in primary hyperparathyroidism (pHPT) is unclear.Methods: We conducted a multicentre randomized open diagnostic intervention phase III trial in adults with primary hyperparathyroidism and indication for surgical treatment. Patients were assigned in a 1:1 ratio...

ea0063oc5.1 | Adrenal 1 | ECE2019

Positive impact of genetic test on the management and outcome of patients with paraganglioma and/or pheochromocytoma

Buffet Alexandre , Aim Laurene Ben , Leboulleux Sophie , Drui Delphine , Vezzosi Delphine , Libe Rossella , Ajzenberg Christiane , Bernardeschi Daniele , Cariou Bertrand , Chabolle Frederic , Chabre Olivier , Darrouzet Vincent , Delemer Brigitte , Desailloud Rachel , Goichot Bernard , Esvant Annabelle , Offredo Lucile , Herman Philippe , Laboureau Sandrine , Lefebvre Herve , Pierre Peggy , Raingeard Isabelle , Reznik Yves , Sadoul Jean-Louis , Hadoux Julien , Tabarin Antoine , Tauveron Igor , Zenaty Delphine , Favier Judith , Bertherat Jerome , Baudin Eric , Amar Laurence , Gimenez-Roqueplo Anne-Paule

Context: Paragangliomas and pheochromocytomas (PPGL) are rare neuroendocrine tumors, characterized by a strong genetic component. Indeed, up to 40% of patients carry a germline mutation in a PPGL susceptibility gene. In accordance with the international recommendations, genotyping of PPGL susceptibility genes is therefore proposed to all patients with PPGL, but it has actually never been shown whether the identification of a germline mutation in one PPGL susceptibility gene ch...