Searchable abstracts of presentations at key conferences in endocrinology

ea0056gp274 | Thyroid non cancer - Benign Thyroid disease/ treatment | ECE2018

Reduced quality of life and persistent complaints in treated hypothyroid patients

Molewijk Ellen , Martens Maayan , Fliers Eric , Zelissen Pierre , Dreijerink Koen , van Dooren Ad , Heerdink Rob

Background: Hypothyroidism is a common endocrine disorder and the standard treatment is replacement therapy with levothyroxine (LT4). Although many hypothyroid patients improve upon treatment with LT4, a proportion seems to experience residual hypothyroid complaints despite treatment, even when plasma TSH and FT4 are within reference ranges.Methods: Using an on-line survey we investigated i) the health-related quality of life (QoL) (ThyPRO), ii) the acti...

ea0056p955 | Female Reproduction | ECE2018

Breast cancer in transgender persons receiving gender affirming hormone treatment: results of a nationwide cohort study

JM de Blok Christel , Wiepjes Chantal M. , Nota Nienke M. , Engelen Klaartje van , Adank Muriel A. , Dreijerink Koen M.A. , Barbe Ellis , Konings Inge R.H.M. , den Heijer Martin

Background: Transpersons can receive gender affirming hormone therapy (HT) to induce physical changes. Little is known about the effect of HT on breast cancer (BC) risk.Objectives: To study the prevalence and characteristics of BC in transpersons with HT and to compare this prevalence with the general Dutch male and female population.Methods: Adult transpersons who were seen after 1991 and started HT in the VUmc were included. This...

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...