Searchable abstracts of presentations at key conferences in endocrinology

ea0006p15 | Clinical case reports | SFE2003

A Case of ACTH Secreting Benign Mediastinal Carcinoid with Hypocalcaemia

Goulden P , Spring M

This 42-year-old male presented with a six-month history of general lethargy and mood changes. He had experienced weakness & difficulty climbing stairs; weight loss; ankle swelling and increased frequency of micturition. There was no significant past medical history.Initial investigations revealed Na+ 144mmol/L (135-145);K+ 2.3mmol/L(3.5-5.2); U 8.8mmol/L (2.6-6.7); Cr 75μmol/L (60-125); TCO2 41mmol/L (21-31); Fasting glucose 7.4mmol/L; TSH 0.21mU...

ea0006dp22 | Diabetes, metabolism and cardiovascular | SFE2003

A Case of ACTH Secreting Benign Mediastinal Carcinoid with Hypocalcaemia

Goulden P , Spring M

This 42-year-old male presented with a six-month history of general lethargy and mood changes. He had experienced weakness & difficulty climbing stairs; weight loss; ankle swelling and increased frequency of micturition. There was no significant past medical history.Initial investigations revealed Na+ 144mmol/L (135-145);K+ 2.3mmol/L(3.5-5.2); U 8.8mmol/L (2.6-6.7); Cr 75μmol/L (60-125); TCO2 41mmol/L (21-31); Fasting glucose 7.4mmol/L; TSH 0.21mU...

ea0004p23 | Clinical case reports | SFE2002

BRONZE DIABETES, IMPOTENCE AND PITUITARY FAILURE, A SPECTRUM OF A GENETIC DISORDER

Haq M , Rich P , Spring M

A 66-year-old Caucasian male presented with polydipsia, profound weight loss, blood glucose of 29.1 millimoles per litre and mild acidosis. Urinalysis revealed no ketonuria. A mild acidosis was also identified. A bronzed skin appearance was noted which together with deranged liver function raised suspicions of haemochromatosis in conjunction with newly diagnosed diabetes. Initial treatment involved rehydration, intravenous then subcutaneous insulin therapy. Subsequent abdomina...

ea0004dp27 | Diabetes, metabolism and cardiovascular | SFE2002

BRONZE DIABETES, IMPOTENCE AND PITUITARY FAILURE, A SPECTRUM OF A GENETIC DISORDER

Haq M , Rich P , Spring M

A 66-year-old Caucasian male presented with polydipsia, profound weight loss, blood glucose of 29.1 millimoles per litre and mild acidosis. Urinalysis revealed no ketonuria. A mild acidosis was also identified. A bronzed skin appearance was noted which together with deranged liver function raised suspicions of haemochromatosis in conjunction with newly diagnosed diabetes. Initial treatment involved rehydration, intravenous then subcutaneous insulin therapy. Subsequent abdomina...

ea0005p35 | Clinical Case Reports | BES2003

Steroid responsive hypervitaminosis D due to sarcoid myopathy

Barnor Q , Haq M , Al-Memar A , Spring M

The mitochondrial enzyme 25-hydroxyvitamin D(sub)3 1-alpha-hydroxylase plays an important role in the synthesis of active 1,25-dihydroxyvitamin D(sub)3 in both renal and extra-adrenal tissues such as granulamatous tissue. There is an increased expression of 1-alpha-hydroxlase in sarcoidosis. This can result in hypercalcaemia secondary to elevated 1,25-dihydroxyvitamin D(sub)3.We present a case of a 81 year old retired GP with long-standing hypercalcaemia associated with a ...