ea0094cc5 | Section | SFEBES2023
Michaelidou Maria
, Phillips Benjamin
, Man Mung Sai
, Al-Hayali Mohammed
, Chen Lilian
, Allcock Rebecca
, Monaghan Phillip
, Thirkettle Sally
, Clarke Noel
, Gulamhusein Aziz
, Beards Sue
, Hoong Ho Jan
, Kaushal Kalpana
, Howell Simon
, Adam Safwaan
Phaeochromocytoma-driven Ectopic ACTH Syndrome (EAS) is rare. We report the case of a 31-year-old female, who presented with abdominal pain and vomiting. She had clinical features of severe Cushings syndrome (proximal myopathy, bruising, refractory hypertension and acute confusion). Admission investigations revealed hypokalaemia (2.1mmol/l [3.5-5.5mmol/l]) and a 4.5cm left adrenal lesion with a bulky right adrenal on CT abdomen. She was diagnosed with hyperte...