Searchable abstracts of presentations at key conferences in endocrinology

ea0086p250 | Neuroendocrinology and Pituitary | SFEBES2022

A case report of Takotsubo cardiomyopathy associated with pituitary apoplexy

Setty Naveen , Hasan Faisal , Parfitt Vernon

Background: We present a rare diagnosis of a patient presenting with Takotsubo cardiomyopathy and pituitary apoplexy. The case highlights the difficulty in management of a cardiac event with bleeding risk in a patient with these associated diagnoses.Case report: An 85-year-old woman was admitted to hospital with a severe frontal headache that woke her from sleep. She described chest pain associated with breathlessness later and was mildly confused. Sadly...

ea0065p101 | Bone and calcium | SFEBES2019

Four cases of familial hypocalciuric hypercalcaemia presenting with severe hypercalcaemia

Jagannatha Hema , Sabin Jodie , Parfitt Vernon

Familial hypocalciuric hypercalcaemia (FHH) usually manifests with mild asymptomatic hypercalcaemia. Presentations with severe hypercalcaemia are uncommon and may be mistakenly assumed to be primary hyperparathyroidism (PHPT) unless detailed testing is undertaken on all cases of hypercalcaemia. We present 4 cases of FHH presenting with severe hypercalcalcaemia, corrected serum calcium (coCalcium) > 3 mmol/l. Three cases were initially admitted to hospital as medical emergencie...

ea0062wa6 | Workshop A: Disorders of the hypothalamus and pituitary | EU2019

Recurrence of Pituitary Apoplexy in non-functioning pituitary adenoma

Jagannatha Hema , Parfitt Vernon , Bradley Karin

79 year old gentleman was reviewed as new patient in the Endocrine clinic. He was diagnosed with Pituitary Apoplexy of a Non-functioning Adenoma in 1998. He was under surveillance and the tumour remained relatively stable with no complications until 2008.Surgical history: There was a gradual increase in the size of the adenoma over 5 years. He underwent Transphenoidal adenectomy in Feb 2014 as the tumour was draped over the optic chiasm. Intra-operativel...

ea0050p064 | Bone and Calcium | SFEBES2017

Milk-alkali syndrome in the post PPI era

Hasan Faisal , Cheyne Elizabeth , Parfitt Vernon , Chau Fong , Tatovic Danijela

The milk – alkali syndrome was well known in the pre-proton pump inhibitor era when remedies for peptic ulcer included a large amount of calcium and sodium bicarbonate resulting in hypercalcaemia, metabolic alkalosis and often acute kidney injury. In a study done from 1998 to 2003, milk alkali syndrome was the cause of hypercalcaemia in 8.8 percent of the cases which is a significant percentage, so awareness about it is important.<p class="abste...

ea0050p412 | Thyroid | SFEBES2017

A rare case of Moyamoya disease in association with Graves Disease in a Caucasian female

Hasan Faisal , Ahmad Shaza , Chau Fong , Parfitt Vernon

Moyamoya disease is a progressive chronic neurological disease due to multiple narrowing of the carotid arteries. It can be seen in association with atherosclerosis, vasculitis, haematological conditions, connective tissue disease, neurocutaneous syndromes and certain autoimmune diseases. Very few cases have been reported in association with Graves disease and the majority being in the East Asian population. We present a rare case of this association in a young C...

ea0050p064 | Bone and Calcium | SFEBES2017

Milk-alkali syndrome in the post PPI era

Hasan Faisal , Cheyne Elizabeth , Parfitt Vernon , Chau Fong , Tatovic Danijela

The milk – alkali syndrome was well known in the pre-proton pump inhibitor era when remedies for peptic ulcer included a large amount of calcium and sodium bicarbonate resulting in hypercalcaemia, metabolic alkalosis and often acute kidney injury. In a study done from 1998 to 2003, milk alkali syndrome was the cause of hypercalcaemia in 8.8 percent of the cases which is a significant percentage, so awareness about it is important.<p class="abste...

ea0050p412 | Thyroid | SFEBES2017

A rare case of Moyamoya disease in association with Graves Disease in a Caucasian female

Hasan Faisal , Ahmad Shaza , Chau Fong , Parfitt Vernon

Moyamoya disease is a progressive chronic neurological disease due to multiple narrowing of the carotid arteries. It can be seen in association with atherosclerosis, vasculitis, haematological conditions, connective tissue disease, neurocutaneous syndromes and certain autoimmune diseases. Very few cases have been reported in association with Graves disease and the majority being in the East Asian population. We present a rare case of this association in a young C...

ea0074ncc28 | Highlighted Cases | SFENCC2021

Cushing’s syndrome and the diagnostic challenge

Wordsworth Georgina , Talbot Fleur , Parfitt Vernon , Chau Fong

Section 1: Case history: This 41 year old lady was seen in the Endocrine clinic with an 8 year history of worsening hypertension, obesity and Type 2 diabetes. She had no conditions known to cause physiological hypercortisolism, no exogenous steroid use and had clear physical features of Cushing’s syndrome.Section 2: Investigations: Investigations confirmed Cushing’s syndrome with two elevated urinary free cortisol assessments (UFC) (934 and 906...

ea0050ep042 | Clinical Biochemistry | SFEBES2017

A rare cause of acute severe hyponatraemia secondary to the syndrome of inappropraite anti-diuretic hormone (SIADH) secretion

Wordsworth Georgina , Hasan Faisal , Parfitt Vernon , Chau Fong , Cheyne Elizabeth , Tatovic Danijela , Lonnen Kathryn , Johnson Andrew

Hyponatremia is the commonest electrolyte abnormality presenting to Medical Admissions and when acute, severe and symptomatic, is associated with high mortality. The syndrome of inappropriate antidiuretic hormone secretion (SIADH) is the most common underlying disorder in hospitalised patients with euvolaemic hyponatraemia and is a complication of many clinical conditions and drug therapies.We discuss the cases of two patients...

ea0050ep042 | Clinical Biochemistry | SFEBES2017

A rare cause of acute severe hyponatraemia secondary to the syndrome of inappropraite anti-diuretic hormone (SIADH) secretion

Wordsworth Georgina , Hasan Faisal , Parfitt Vernon , Chau Fong , Cheyne Elizabeth , Tatovic Danijela , Lonnen Kathryn , Johnson Andrew

Hyponatremia is the commonest electrolyte abnormality presenting to Medical Admissions and when acute, severe and symptomatic, is associated with high mortality. The syndrome of inappropriate antidiuretic hormone secretion (SIADH) is the most common underlying disorder in hospitalised patients with euvolaemic hyponatraemia and is a complication of many clinical conditions and drug therapies.We discuss the cases of two patients...