Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep90 | Adrenal and Cardiovascular Endocrinology | ECE2023

Multifocal paraganglioma due to SDHB mutation: On purpose of one clinical case

Ferreira-Ocampo Pablo , Doejo Marciales Sandra Carolina , Barra Malig Solange Fabiola , Astunague Condori Remy Edward , Chicharro Pablo Lois , Ruiz Francisca Almodovar , Gorgojo Martinez Juan Jose , Salinas Helena Requejo

The mutations of succinate dehydrogenase subunits (SDHA, SDHB, SDHC, SDHD) are linked with a predisposition to develop pheochromocytoma and paraganglioma, often in diferent locations of the body. With greater acces to genetic tests, current estimations suggest that 40-50% of pheocromocytoma and paraganglioma cases are inherited and half of them are due to SDH mutations. These mutations can be associated with other tumours like renal carcinomas, gastrointestinal stroma tumours ...