Searchable abstracts of presentations at key conferences in endocrinology

ea0012oc18 | Pituitary, ovary and steroids | SFE2006

Adult onset diabetes insipidus due to congenital midline defects of the brain

Zachariah S , Hyer S

A 30 year old gentleman presented with long standing symptoms of polyuria and polydypsia and poor libido. On examination he was short (155 cm), weighed 108 kg with a body mass index of 45.1. Investigations revealed normal Blood Glucose, renal function, liver function and calcium. Water deprivation test confirmed the diagnosis of Cranial Diabetes Insipidus. He was started on DDAVP tablets 100 microgram’s twice daily. Further tests showed a normal IGF-1, synacthen test and ...

ea0012p74 | Pituitary | SFE2006

Anaemia: A rare presenting feature of pituitary tumour

Zachariah S , Rodin A

A 40 year old gentleman presented to his GP with a 12 month history of tiredness and breathlessness on playing basketball with his son. Initial investigations revealed he had a normocytic anaemia with haemoglobin of 9.8 and white cells and platelets were normal. He was referred to the Gastroenterologists and had normal renal function, liver function, bone profile, ESR and serum electrophoresis. His B12, folate and ferritin were normal. CT Abdomen was normal and duodenal biopsy...

ea0010p5 | Clinical case reports/Governance | SFE2005

Autoimmune Addison’s disease in identical twins

Zachariah S , Russell-Jones D

Autoimmune adrenal insufficiency may be familial or non familial. We report a case of identical female twins, both with Addison’s disease and detectable antibodies to adrenal cortex.Case report: Twin A at age of 27 developed Addison’s disease and hypothyroidism. She was found to be positive for anti-adrenal antibodies, anti-thyroid antibodies and intrinsic factor auto antibodies. Therefore Twin B was tested for the same auto antibodies and was ...

ea0015p203 | Neuroendocrinology and behaviour | SFEBES2008

Carcinoid syndrome presenting as chronic diarrhoea in a 88 year old lady with possible primary in the liver

Koshi I , Zachariah S , Schiff R

We present the case of 88 year old lady who presented with long standing history of diarrhoea (18 months). She had been previously investigated under the gastroenterologists with various tests including upper GI endoscopy and colonoscopy. In view of deterioration of symptoms she was admitted under the geriatric team as she could no longer cope with the diarrhoea. On examination she looked well and had fullness in the right hypochondrial region. Blood tests showed abnormal live...

ea0011p220 | Cytokines and growth factors | ECE2006

Effects of IGF-2 on glucose metabolism

Zachariah S , Brackenbridge A , Russell Jones D

The effects of IGF-2 on glucose homeostasis have been more understood from individuals with fasting hypoglycaemia associated with non-islet cell tumours. Endogenous IGFs which circulate in adults fail to exert their immense potential hypoglycaemic activity because they are largely trapped within the vascular space due to their sequestration in a high molecular weight protein complex. The tumours produce excessive amounts of ‘big IGF-2’ which is less readily bound by ...

ea0009p191 | Clinical | BES2005

Ulcerative colitis presenting after bilateral adrenalectomy

Zachariah S , Wright J , Russell-Jones D

Patients with Cushing's disease have high levels of circulating corticosteroids. Treatment may result in unmasking of steroid dependant conditions. We report a case of ulcerative colitis presenting after bilateral adrenalectomy.Case reportA 19 year old girl underwent bilateral adrenalectomy in November 1998 for pituitary dependant Cushing's disease. She was discharged on hydrocortisone and fludrocortisone and post operatively her c...

ea0006p33 | Endocrine tumours and neoplasia | SFE2003

PHAEOCHROMOCYTOMA AND MULTIFOCAL GASTROINTESTINAL STROMAL TUMOURS:CARNEY TRIAD VARIANT OR A NEW SYNDROME?

Zachariah S , Bano G , Nussey S

Case: A GP with autoimmune hypothyroidism presented with a phaeochromocytoma during labour at the age of 36 y. A left adrenalectomy confirmed the diagnosis and a basal cell carcinoma was also removed. She had a history of Dupuytren's lesions of both soles and palms starting in her teenage years and multiple keratosis. There was no family history of any endocrine or skin disorder. At 41y, a benign breast lump was removed and also a gastrointestinal spindle cell stromal tumour (...

ea0006dp18 | Diabetes, metabolism and cardiovascular | SFE2003

PHAEOCHROMOCYTOMA AND MULTIFOCAL GASTROINTESTINAL STROMAL TUMOURS:CARNEY TRIAD VARIANT OR A NEW SYNDROME?

Zachariah S , Bano G , Nussey S

Case: A GP with autoimmune hypothyroidism presented with a phaeochromocytoma during labour at the age of 36 y. A left adrenalectomy confirmed the diagnosis and a basal cell carcinoma was also removed. She had a history of Dupuytren's lesions of both soles and palms starting in her teenage years and multiple keratosis. There was no family history of any endocrine or skin disorder. At 41y, a benign breast lump was removed and also a gastrointestinal spindle cell stromal tumour (...