Searchable abstracts of presentations at key conferences in endocrinology

ea0091cb63 | Additional Cases | SFEEU2023

A Young Woman with Symptomatic Primary Hyperparathyroidism and a Renal Stone

Khan Shaila , Palazzo Fausto , Haboosh Sara , Behary Presheela , Wernig Florian , Cox Jeremy , Comninos Alexander

A 27-year old Caucasian woman was referred to the Endocrine Bone Clinic after investigations for general malaise revealed hypercalaemia and elevated parathyroid hormone levels. She had no history of constipation, abdominal pain, bone pain, or other related symptoms. She had no history of renal stones or fractures and no change in weight. Her past medical history included asthma and she took a salbutamol inhaler as required. She had no family history of endocrine pathology. Gen...

ea0065p5 | Adrenal and Cardiovascular | SFEBES2019

Cardiovascular morbidity is increased in secondary but not primary adrenal failure

Ngaosuwan Kanchana , Godsland Ian , Cox Jeremy , Majeed Azeem , Quint Jennifer , Johnston Desmond , Robinson Stephen

Background: Increased cardiovascular mortality and evidence of atherosclerosis have been reported in patients with pituitary disorders, irrespective of type of pituitary hormone deficiency. However, there are few data on cardiovascular events in patients with secondary adrenal failure due to pituitary disease compared with those who have primary adrenal failure.Subjects: 2052 patients with primary adrenal failure were compared with 20 366 matched control...

ea0065p114 | Bone and calcium | SFEBES2019

Intermittent Hypercalcaemia in a Young Man

Almazrouei Raya , Cox Jeremy , Fraser William D , Tang Jonathan , Comninos Alexander N

A 33 year-old man was referred to the endocrine bone clinic following presentation with a 4 mm kidney stone and hypercalcaemia. Apart from mild fatigue, he had no other hypercalcaemic or concerning symptoms. He was not on any medications or supplements. He had a positive family history for kidney stones and reported that his grandmother had been noted to have hypercalcaemia in the past. There was significant consanguinity in his family. Examination was entirely normal while bl...

ea0048wf10 | Workshop F: Disorders of the parathyroid glands, calcium metabolism and bone | SFEEU2017

Severe hypercalcaemia and osteoporosis in a patient with primary hyperparathyroidism

Ramli Rozana , Robinson Stephen , Yee Michael , Palazzo Fausto , Cox Jeremy PD , Comninos Alexander N

A 60-year-old Caucasian lady was referred to the metabolic bone clinic for assessment of osteoporosis. Her risk factors for osteoporosis included gender, postmenopausal status, childhood immobility due to illness, previous severe vitamin D deficiency, COPD, as well as an extensive smoking and alcohol history. She had multiple previous fragility fractures involving her ribs and both radii. A DEXA scan revealed lumbar osteoporosis (T -4.0) and femoral osteopenia (T -2.0). Thorac...

ea0028p80 | Clinical practice/governance and case reports | SFEBES2012

Renal calculi as a presenting feature in a patient with familial hypocalciuric hypercalcaemia (FHH).

Reddy Monika , Tanday Raj , Feeney Claire , Darko Daniel , Hadjiminas Dimitri , Cox Jeremy

A 46-year-old Columbian man, with a previous history of pulmonary sarcoid and renal calculi in 2001, was referred to the Endocrinology clinic in 2005 with persistent hypercalcaemia despite successful treatment of the sarcoid. The initial hypercalcaemia work-up results were as follows: adjusted calcium 2.96 (2.15–2.60), parathyroid hormone (PTH) 9.0 pmol/l (1.1–6.8), 25-(OH)2 vitamin D 71 nmol/l (>50), magnesium 0.99mmol/l (0.65–1.00), creatinine 97 umol/l...

ea0021p219 | Endocrine tumours and neoplasia | SFEBES2009

MEN2B patients with a RET A883F mutation have less aggressive MTC than those with the common RET M918T mutation

Worth Gabriella , Palazzo Fausto , Tolley Neil , Robinson Stephen , Cox Jeremy , Williams Graham , Bassett Duncan

MEN2B is the most aggressive form of MEN2. Consequently, the new American Thyroid Association guidelines recommend prophylactic thyroidectomy early in the first year of life. Ninety-seven percentage of MEN2B cases result from a germline methionine to threonine mutation at codon 918 (M918T) of the RET proto-oncogene. In addition, an exceedingly rare alanine to phenylalanine mutation at codon 883 (A883F) has been reported in 4 unrelated adults. In each case metastatic MTC and th...

ea0073oc1.6 | Oral Communications 1: Adrenal and Cardiovascular Endocrinology | ECE2021

All-cause mortality in adrenal insufficiency patients using prednisolone or hydrocortisone replacement

Ngaosuwan Kanchana , Johnston Desmond , Godsland Ian , Cox Jeremy , Oliver Azeem , Quint Jennifer , Oliver Nick , Robinson Stephen

BackgroundWhilst hydrocortisone is standard glucocorticoid replacement therapy in patients with adrenal insufficiency, some have considered prednisolone an alternative. Some data have shown diabetes and osteoporosis risk. Mortality of patients using prednisolone in relation with those using hydrocortisone is not known. We compared all-cause mortality risk compared to matched controls in patients with primary or secondary adrenal insufficiency using predn...

ea0073pep11.7 | Presented ePosters 11: Adrenal and Cardiovascular Endocrinology | ECE2021

All-cause mortality in adrenal insufficiency patients with primary and secondary adrenal insufficiency

Ngaosuwan Kanchana , Johnston Desmond , Godsland Ian , Cox Jeremy , Majeed Azeem , Quint Jennifer , Oliver Nick , Robinson Stephen

BackgroundIncreased mortality risk of patients with adrenal insufficiency has been inconsistently reported. This might have resulted from the disparity of time and place of clinical care between the study patients and reference population. Also, data of patients with secondary adrenal insufficiency was limited as majority focused on other types of pituitary disorders. Therefore, we compared all-cause mortality of patients with primary and secondary adren...

ea0073aep662 | Thyroid | ECE2021

An audit of thyroidectomy in Graves’ Disease, in a large UK tertiary centre

Jones Larissa , Khan Shaila , Tolley Neil , Palazzo Fausto , Cox Jeremy , Agha-Jaffar Rochan , Robinson Stephen

BackgroundThyrotoxicosis with Graves’ Disease is treated with thionamide, radio-iodine treatment and thyroidectomy. Surgery is an important choice, especially when Graves’ Disease is complicated by thyroid orbitopathy. Pre- and post-operative protocols for thyroidectomy are imperative.Aims1) To assess pre-operative preparation of patients, with potassium iodide, vitamin D, beta blockade, and the pre...

ea0074ncc18 | Highlighted Cases | SFENCC2021

A case of iatrogenic Cushing’s disease and secondary adrenal insufficiency following a drug interaction between intra-articular triamcinolone injection and ritonavir

Khan Shaila , Walsh John , Cox Jeremy , Agha-Jaffar Rochan , Gable David

Section 1: Case history: A 50-year-old woman presented to the HIV clinic after suspecting adverse effects following two intra-articular triamcinolone injections to her left hip, administered three and seven months prior. She complained of ongoing leg pain, generalised weakness and lethargy. Her past medical history included HIV infection, mild asthma for which she took inhalers only and had never required oral steroids. Her antiretroviral medications included dolutegravir, dar...