Searchable abstracts of presentations at key conferences in endocrinology

ea0099p227 | Adrenal and Cardiovascular Endocrinology | ECE2024

CXCR4-directed [68Ga]Ga-PentixaFor PET/CT as a diagnostic modality in subtyping primary aldosteronism

Baz Amir Hosse in Chaman , Gotthardt Martin , Spiering Wilko , Deinum Jaap , Langenhuijsen Johannes

Introduction: Primary aldosteronism (PA) is a form of secondary hypertension, affecting 2.4% of the hypertensive population. It is caused by autonomous overproduction of aldosterone by either a unilateral aldosterone-producing adenoma (APA) or by bilateral adrenal hyperplasia (BAH). Subtyping is crucial, because PA is cured by adrenalectomy in APA and is treated by medication in BAH. The reference standard in subtyping PA is adrenal vein sampling (AVS). However, it is invasive...

ea0099rc7.1 | Rapid Communications 7: Endocrine-related Cancer | ECE2024

PRAP study - Partial versus radical adrenalectomy for hereditary pheochromocytomas

Xu Kai , Langenhuijsen Johannes , Vietor Charlotte , Feelders Richard , van Ginhoven Tessa , Elhassan Yasir , Bioletto Fabio , Parasiliticaprino Mirko , Zandee Wouter , Kruijff Schelto , AEkerstrom Tobias , Pamporaki Christina , Bechmann Nicole , Lussey-Lepoutre Charlotte , Canu Letizia , Steenaard Rebecca , Driessens Natacha , Velema Marieke , Dreijerink Koen , Engelsman Anton , Timmers Henri , de Laat Marieke

Introduction: Pheochromocytoma, a rare catecholamine-secreting adrenal tumor, can cause hypertension and life-threatening complications. Hereditary cases have an increased risk of developing bilateral disease. Standard treatment involves radical adrenalectomy, leading to adrenal insufficiency in bilateral cases. Partial adrenalectomy aims to preserve adrenal function but has higher recurrence rates. This study compares outcomes of partial vs radical adrenalectomy in hereditary...