Searchable abstracts of presentations at key conferences in endocrinology

ea0086p251 | Neuroendocrinology and Pituitary | SFEBES2022

ACTH dependent Cushing’s syndrome due to a pituitary macroadenoma presenting with acute Type B aortic dissection, severe hypercortisolism and resistant hypertension

Goldstein Dovid , Platts Stephen , Mofidi Reza , Varma Anil , Nag Sath

Introduction: Cushing’s syndrome is a known risk factor for aortic dissection but the association of these conditions is rare. Hypercortisolism is associated with an increased risk of cardiovascular disease and accounts for the high morbidity & mortality in untreated patients.Case Study: A 64y old male presented with acute onset chest pain, radiating to the back. CT angiogram showed Stanford Type B dissection involving the distal aortic arch/des...

ea0059ep82 | Neuroendocrinology and pituitary | SFEBES2018

Acromegaly due to a mixed growth hormone secreting adenoma-gangliocytoma - a rare cause of GH excess

Wood Maximilian , Varma Anil , Scoones David , Nag Sath

Adeno-gangliocytomas are rare tumours of the pituitary gland with less than 40 cases described worldwide. Due to the rarity of these tumours, treatment modalities largely follow that of conventional therapies for common pituitary lesions. Case reports on these tumours offer insight into their presentation and the effectiveness of treatment which helps guide future management. A 64-year-old man was admitted for stone fragmentation and ureteric stent insertion. During anaestheti...