Searchable abstracts of presentations at key conferences in endocrinology

ea0099ep14 | Endocrine-Related Cancer | ECE2024

Machine Learning-based Online Survival Prediction Tool for Adrenocortical Carcinoma

Sedar Saygili Emre , S Elhassan Yasir , Prete Alessandro , Lippert Juliane , Altieri Barbara , L Ronchi Cristina

Background: Adrenocortical carcinoma (ACC) is a rare endocrine cancer. We aimed to develop machine learning (ML) models for predicting clinical outcomes of patients with ACC and deploy them as a web-based decision support tool. Methods: The S-GRAS dataset1 was used as a training cohort (n=942), while the COMBI dataset2 and new patients were used as a validation cohort (n=220). We used S-GRAS parameters previously d...

ea0086p25 | Adrenal and Cardiovascular | SFEBES2022

Coincidence of Primary Adrenocortical Carcinoma and Melanoma: Three Case Reports

Lynn Ko Ye , Kumar Vaishnavi , Lippert Juliane , Diaz-Cano Salvador , Skordilis Kassiani , Kimpel Otilia , Kircher Stefan , Asia Miriam , S. Elhassan Yasir , Altieri Barbara , L. Ronchi Cristina

Adrenocortical carcinoma (ACC) is a rare endocrine malignancy. ACC may rarely occur as part of familial cancer syndromes, but the majority of the cases occur sporadically. A significant proportion of sporadic ACC cases may be preceded by other malignancies and adrenal metastasis from these primary tumours may frequently occur. Herein we present three cases where sporadic ACC was identified in patients with coexistent or previous history of melanoma.Case ...

ea0099ep919 | Adrenal and Cardiovascular Endocrinology | ECE2024

Primary unilateral macronodular adrenal hyperplasia with concomitant glucocorticoid and androgen excess and KDM1A inactivation

Elhassan Yasir , Appenzeller Silke , Landwehr Laura-Sophie , Lippert Juliane , Popat Dillon , C. Gilligan Lorna , Abdi Lida , Goh Edwina , Diaz-Cano Salvador , Kircher Stefan , Gramlich Susanne , Sutcliffe Robert , Thangaratinam Shakila , Chan Li , Fassnacht Martin , Arlt Wiebke , L Ronchi Cristina

Background: Primary bilateral macronodular adrenal hyperplasia (PBMAH) is a rare cause of Cushing’s syndrome. Primary unilateral macronodular adrenal hyperplasia with concomitant glucocorticoid and androgen excess has never been studied before.Methods: We investigated a woman with a large, heterogeneous 7 cm adrenal mass (with a radiologically normal contralateral adrenal) and adrenocorticotropic hormone (ACTH)-independent glucocorticoid and androge...