ESPE Abstracts

Background: Phaeochromocytoma is a rare neuroendocrine tumour originating from chromaffin cells in the adrenal medulla and less commonly from extra-adrenal paraganglia. Phaeochromocytoma occur in the context of a genetic syndrome in approximately 50% of adults and 80% of children. Genetic testing of index cases enables testing of first-degree relatives, identification of children who inherit the gene change and surveillance, early diagnosis and treatment of as...