Searchable abstracts of presentations at key conferences in endocrinology

ea0044ep43 | (1) | SFEBES2016

Navigating troubled waters: Hyperglycaemic Hyperosmolar State precipitated by Nephrogenic Diabetes Insipidus

Avari Parizad , Sharma Aditi , Samarasinghe Suhaniya , Barnor Quirinius

Hyperglycaemic hyperosmolar state (HHS) is a common medical presentation, typically occurring in older patients with Type 2 diabetes mellitus. Mortality rates have been reported to be up to 60%. Precipitating factors include dehydration, sepsis, cardiovascular disease and drugs. Here, we describe a rare case of HHS, likely to have been precipitated following the development of lithium-induced nephrogenic diabetes insipidus (DI).A 62-year-old female prese...

ea0048cp13 | Poster Presentations | SFEEU2017

ACTH-dependent Cushing’s syndrome unmasked following transphenoidal surgery for Acromegaly – the rare coexistence of dual endocrinopathies

Avari Parizad , Sharma Aditi , Barnor Quirinius , Galliford Thomas , Ogilvie Arla , Kong Chantal

Case history: We describe a rare case of a 59-year-old woman, whose hypercortisolism was unmasked following transphenoidal surgery for Acromegaly. She presented to the Endocrine Clinic in 2006 with acromegalic features and MRI revealing a pituitary macroadenoma 20×18×18 mm. Repeat dynamic evaluation showed inadequate GH suppression (initially normal), raising the possibility of early rumbling Acromegaly. 0900 h serum cortisol was 287 nmol/l. She was started on Caberg...

ea0044cc10 | Featured Clinical Cases | SFEBES2016

ACTH-dependent Cushing’s syndrome unmasked following transphenoidal surgery for Acromegaly – the rare coexistence of dual endocrinopathies

Avari Parizad , Sharma Aditi , Barnor Quirinius , Galliford Thomas , Ogilvie Arla , Kong Chantal

Coexistence of Acromegaly with Cushing’s syndrome in the same individual is rare. We herein describe a case of a 59-year-old woman, whose hypercortisolism was unmasked following transphenoidal surgery for Acromegaly.She presented to the Endocrine Clinic in 2006 with acromegalic features and MRI revealing a pituitary macroadenoma 20×18×18 mm. Repeat dynamic evaluation showed inadequate GH suppression (initially normal), raising the possibil...