Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep1168 | Late Breaking | ECE2022

A rare case of hypocortisolism in hypercoagulable state

Htet Aung Htet , Zeeshan Amna , Chernov Dmitriy , Damani Nizar , Tauni Rahat , Kostoula Melina

We report a case of 39-year-old woman presenting with sudden severe abdominal pain and vomiting. She had a past medical history of anti-phospholipid antibody syndrome (APLS) diagnosed in the United States (US) 20 years ago. She had multiple episodes of vomiting over the last 10 years and was diagnosed with cyclical vomiting as investigations including CT abdomen and endoscopy did not reveal a structural cause. She was taking warfarin for APLS. She was haemodynamically stable a...

ea0050ep060 | Neoplasia, Cancer and Late Effects | SFEBES2017

A rare case of MEN 4 presenting with hypercalcaemia in a patient with microprolactinoma 6 years after the diagnosis

Alexiadou Kleopatra , Devendra Devasenan , Galliford Thomas , Owens Martina , Bussell Anne-Marie , Damani Nizar , Ogilvie Arla

Multiple Endocrine Neoplasia is characterised by the occurrence of tumours involving two or more endocrine glands within a single patient. MEN are autosomal dominant disorders. Four forms have been described: MEN 1 due to menin mutations, MEN2 (previously MEN2A) due to mutations of a tyrosine kinase receptor encoded by the rearranged during transfection (RET) protoncogene, MEN3 (previously MEN2B) due to RET mutations and MEN4 due to cyc...

ea0050ep060 | Neoplasia, Cancer and Late Effects | SFEBES2017

A rare case of MEN 4 presenting with hypercalcaemia in a patient with microprolactinoma 6 years after the diagnosis

Alexiadou Kleopatra , Devendra Devasenan , Galliford Thomas , Owens Martina , Bussell Anne-Marie , Damani Nizar , Ogilvie Arla

Multiple Endocrine Neoplasia is characterised by the occurrence of tumours involving two or more endocrine glands within a single patient. MEN are autosomal dominant disorders. Four forms have been described: MEN 1 due to menin mutations, MEN2 (previously MEN2A) due to mutations of a tyrosine kinase receptor encoded by the rearranged during transfection (RET) protoncogene, MEN3 (previously MEN2B) due to RET mutations and MEN4 due to cyc...