Searchable abstracts of presentations at key conferences in endocrinology

ea0063ep6 | Adrenal and Neuroendocrine Tumours | ECE2019

A case of Cushing syndrome due to primary bilateral macronodular adrenal hyperplasia caused by ARMC5 mutation and concomitant primary hyperparathyroidism

Mamedova Elizaveta , Vasilyev Evgeny , Petrov Vasily , Izmailova Natalya , Buryakina Svetlana , Rozhinskaya Liudmila , Tiulpakov Anatoly , Belaya Zhanna

Primary bilateral macronodular adrenal hyperplasia (PBMAH) is a rare cause of Cushing syndrome and in 25–55% of cases is caused by mutations in ARMC5 gene. A 37 y.o. female was referred to our center with a diagnosis of ACTH-independent Cushing syndrome. Laboratory testing confirmed endogenous hypercortisolism (urinary free cortisol 5063.5 nmol/24 h (60–413), midnight salivary cortisol 56.6 nmol/l (0.5–9.4), midnight serum cortisol 1427 nmol/l (46–...