Searchable abstracts of presentations at key conferences in endocrinology

ea0094p243 | Neuroendocrinology and Pituitary | SFEBES2023

A rare case of phaeochromocytoma secondary to Phosphatase and Tensin Homolog (PTEN) mutation

Narula Kavita , Lazarus Katharine , Sharma Bhavna , Yang Wei , Alexiadou Kleopatra , Avari Parizad , Hui Elaine , Desouza Bianca , Tan Tricia

A 65-year-old female with PTEN Hamartoma Tumour Syndrome, Follicular thyroid carcinoma, and Endometrial Carcinoma, presented at a tertiary centre due to an asymptomatic adrenal lesion. Previous genetic testing for phaeochromocytoma and paraganglioma in 2020 showed no pathogenic variants in multiple genes (FH, MAX, MEN1, SDHx, SDHAF2, TMEM127, VHL, RET gene). Recent imaging revealed a 9 cm left supra-renal lesion that had been gradually increasing in size since 2010. Plasma nor...