Searchable abstracts of presentations at key conferences in endocrinology

ea0006p31 | Endocrine tumours and neoplasia | SFE2003

CYCLOSPORIN A ENHANCES CERAMIDE SIGNALLING IN HUMAN BREAST CANCER CELLS IN RESPONSE TO N-(4-HYDROXYPHENYL) RETINAMIDE

Abbara A , Schrey M

Combination chemotherapy for breast cancer offers the potential for improving drug efficacy through enhancement of cancer cell killing. Theoretically, the mechanistic basis underlying this approach may depend on multiple targets and/or amplification/interaction of putative proapoptotic signals. The synthetic retinoid N-(4-hydroxyphenyl) retinamide (4HPR) has proved effective as a chemopreventative and therapeutic agent in breast cancer, however, the mechanisms mediating this a...

ea0050ep102 | Thyroid | SFEBES2017

Persisting biochemical thyrotoxicosis due to biotin supplementation in a patient with Graves’ disease

Nogueira Edson F , Abbara Ali , Tan Tricia , Comninos Alexander N

A 46-year-old lady was referred to endocrinology with thyrotoxicosis. She was diagnosed with Graves’ disease by her GP in October 2016 when presenting with classical symptoms and investigations [TSH<0.01 mIU/L (NR 0.3–4.2), fT4=34.3 pmol/L (NR 9–23), TSHrAb>30 u/mL (NR<0.4), and increased iodine uptake]. She was therefore started on carbimazole 15 mg/day. She returned to her GP in December 2016 reporting resolved symptoms, however, she ...

ea0050ep102 | Thyroid | SFEBES2017

Persisting biochemical thyrotoxicosis due to biotin supplementation in a patient with Graves’ disease

Nogueira Edson F , Abbara Ali , Tan Tricia , Comninos Alexander N

A 46-year-old lady was referred to endocrinology with thyrotoxicosis. She was diagnosed with Graves’ disease by her GP in October 2016 when presenting with classical symptoms and investigations [TSH<0.01 mIU/L (NR 0.3–4.2), fT4=34.3 pmol/L (NR 9–23), TSHrAb>30 u/mL (NR<0.4), and increased iodine uptake]. She was therefore started on carbimazole 15 mg/day. She returned to her GP in December 2016 reporting resolved symptoms, however, she ...

ea0028p370 | Thyroid | SFEBES2012

Acute bulbar palsy in association with Graves thyrotoxicosis

Abbara Ali , Chhina Navpreet , Joharatnam Jalini , Todd Jeannie , Williams Graham

A 77 year old man with a background of Crohns disease requiring ileostomy, pernicious anaemia and hypertension, presented with a 4month history of dysphagia to solids, hoarseness of voice, anorexia and marked weight loss of 30 kg. He was initially referred to gastroenterology, who performed an endoscopy which was normal. Subsequently he was referred to the ENT and speech and language therapy departments. A video fluoroscopy confirmed severe oropharyngeal dysphagia with effortf...

ea0028p372 | Thyroid | SFEBES2012

Langerhans cell histiocytosis and Graves’ disease

Abbara Ali , Chhina Navpreet , Joharatnam Jalini , Tharakan George , Todd Jeannie

A 27 year old lady with a background of Langerhans cell histiocytosis (LCH) presented to endocrinology clinic for investigation of thyrotoxicosis. At the age of three years old, she presented with a rash on her forehead, which on biopsy revealed Langerhans cell histiocytosis. She was also noted to have symptoms consistent with diabetes insipidus, for which she remains on desmopressin therapy. At the age of six she received pituitary radiotherapy and 6 years ago developed secon...

ea0028p381 | Thyroid | SFEBES2012

Alemtuzamab induced thyrotoxicosis

Chhina Navpreet , Abbara Ali , Joharatnam Jalini , Todd Jeannie

A 60year old gentleman was referred to endocrine team with new onset hyperthyroidism. He had developed tubulointerstitial nephritis secondary to carbamazepine resulting in ESRF 3 years previously. Four months prior to presentation he received a live-unrelated renal transplant including a single dose of Alemtuzamab post-operatively for induction of immunosuppression. Thereafter his immunosuppression was maintained with tacrolimus. Other medical history included bipolar disorder...

ea0025p349 | Thyroid | SFEBES2011

A novel prospective ocular manifestation of Graves’ disease

Abbara Ali , Rajakulasingam Ramya , Hui Elaine , Wynne Katie , Meeran Karim

A 31-year-old engineer presented with a 6-week history of tremor, weight loss, mild goitre and palpitations. At the onset of these symptoms, he also presented to a specialist eye hospital for difficulty with focussing his vision. He had no past medical history and was taking no medications. He did not have any family history of ocular or autoimmune conditions and was a non-smoker. On examination his BMI was 20, he had very mild proptosis, no diplopia and a diffuse symmetrical ...

ea0025p350 | Thyroid | SFEBES2011

Sialorrhoea: an uncommon symptom of Graves’ disease

Mills Rebecca , Abbara Ali , Hui Elaine , Meeran Karim , Wynne Katie

A 47-year-old afrocaribbean lady was referred to endocrinology clinic with a 1-month history of weight loss, heat intolerance, palpitations, fatigue and hair loss. She reported symptoms consistent with proximal myopathy including myalgia and difficulty rising from chairs. Interestingly she noted a 1-month history of hypersalivation, which had caused her significant distress in her social and work life. The hypersalivation had resulted in a change in her voice and had also inte...

ea0018p34 | (1) | MES2008

A potential complication of radiotherapy for acromegaly

Lecamwasam Varunika , Abbara Ali , Bell Richard , Baynes Kevin , Rafique Akkib

Case report: A 40-year-old lady was diagnosed with acromegaly in 1993 after presentation with clinical symptoms. Imaging showed a 1 cm pituitary lesion and she underwent transphenoidal hypophysectomy in 1993. Post-operatively she was rendered hypopituitary, but still had biochemical evidence of active acromegaly. She proceeded to external beam radiotherapy and was started on bromocriptine medical therapy.On routine review in 2006, her acromegaly was bioc...

ea0050ep024 | Bone and Calcium | SFEBES2017

An Unusual Case of Hypercalcaemia Whilst Severely Hypomagnesaemic

Alkaabi Fatima , Naqvi Ali , Lim Chong , Abbara Ali , Comninos Alexander N , Cox Jeremy

A 68-year-old woman presented with a several month history of nausea, confusion and generalised weakness. In addition, she reported decreased appetite with significant weight loss. She did not report any convulsions, abdominal pain, palpitations, or diarrhoea. Significant past medical history included well-controlled T2DM, hypertension, vitamin D deficiency and GI reflux disease. Importantly, she had no history of renal disease. Relevant medications incl...