Searchable abstracts of presentations at key conferences in endocrinology

ea0013p87 | Clinical practice/governance and case reports | SFEBES2007

Radioactive Iodine (I-131) and its effectiveness in treating benign thyroid disease

Patel Kishor , Kalk John

Background: As thyrotoxicosis is associated with significant morbidity, treatment and ultimately cure is essential. Along with anti-thyroid medication and surgery, the use of radioactive Iodine (I-131) has long been established. However, opinion still varies as to when to use I-131, in which patients and whether to give a fixed or tailored dose. To see if our practice was consistent with published data, we conducted an audit of patients treated with I-131 for benign thyroid di...

ea0028p277 | Pituitary | SFEBES2012

Recurrent neutropenia associated with the use of dopamine agonists

Butt Muhammad , Waheed Najeeb , Kalk John

A 38 year lady was referred with a five month history of secondary amenorrhea, galactorrhoea, failure to conceive and elevated prolactin levels of 2023 miu/L (reference 102–496 miu/L). She could not undertake an MRI scan of the pituitary gland as she was claustrophobic and hence a CT scan was performed which did not show and gross pituitary lesion. Microprolactinoma was diagnosed and she commenced bromocriptine. She had normal white blood cells and neutrophil count prior ...

ea0056p722 | Clinical case reports - Pituitary/Adrenal | ECE2018

Sever protracted hypernatraemia following Hyperosmolar hyperglycaemic state: Case report

Omer Tahir , Western Thomas , Kalk John

Introduction: Nephrogenic diabetes insipidus is caused by a deficiency in the action of anti-diuretic hormone, and can be life threatening if not treated appropriately. Lithium is a commonly used mood stabiliser in psychiatry and is known to cause NDI in around 12% of patients. It has been reported in the literature that severe hyperglycemic state may trigger symptomatic lithium-induced NDI in patients who had been on prolonged lithium therapy.Case: We r...

ea0041ep636 | Endocrine tumours and neoplasia | ECE2016

Hyperparathyroidism-jaw tumour syndrome in Adolescence

Hafeez Saba , Kalk John , Saqib Aaisha , Izzat Louise

Introduction: The hyperparathyroidism-jaw tumour syndrome is a rare autosomal, dominantly inherited disorder characterized by neoplastic or cystic lesions in parathyroid gland, jaws and the kidneys. With approximately 200 reported cases in literature this condition remains a challenge both diagnostically and in guiding further management.Case report: Seventeen year old scholar was seen by the maxillofacial department at Medway Hospital with 2 painless sw...