Searchable abstracts of presentations at key conferences in endocrinology

ea0013p45 | Clinical practice/governance and case reports | SFEBES2007

Di-George syndrome presenting as hypocalcaemia in adulthood

Hunter Steven , Johnston Philip , Morrison Patrick

A 29 year old female presented with a two year history of recurrent numbness and tingling in her hands. Trousseau’s sign was positive. Investigations confirmed hypocalcaemia with serum calcium 1.64 nmol/L (2.10–2.60), phosphate 1.23 nmol/L (0.80–1.55), alkaline phosphatase 82 U/L (35–120). Parathyroid hormone was inappropriately normal at 36 pg/ml (10–65), Vitamin D 78 nmol/L (50–75). Her mother reported a history of hypocalcaemia when she was two...

ea0037ep746 | Pituitary: clinical | ECE2015

The effect of intra-articular glucocorticoid injections on hypothalamic-pituitary-adrenal-axis function: a review

Johnston Philip C , Lansang M Cecilia , Chatterjee Soumya , Kennedy Laurence

Background: The use of intra-articular (IA) glucocorticoids for reducing pain and inflammation in patients with osteoarthritis, rheumatoid arthritis, and other inflammatory arthropathies is widespread among primary care physicians, specialists and non-specialists in the United States. Injectable glucocorticoids have anti-inflammatory and analgesic properties which can be effective in improving clinical parameters such as pain, range of motion, and quality of life. After inject...

ea0037ep1176 | Clinical Cases–Pituitary/Adrenal | ECE2015

Ectopic ACTH-secreting pituitary adenomas located in the sphenoid sinus: an overview

Johnston Philip C , Kennedy Laurence , Weil Robert J , Hamrahian Amir

Background: Ectopic pituitary adenomas are defined by the presence of adenomatous pituitary tissue outside the sella and distinctly separate from the pituitary gland. Ectopic ACTH-secreting pituitary adenomas (EAPAs) are a rare cause of Cushing’s syndrome. Detecting these radiologically can prove difficult, in part, due to their typically small size and unpredictable anatomical location.Aim: We reviewed the current literature on all previously repor...

ea0037ep1177 | Clinical Cases–Pituitary/Adrenal | ECE2015

Cushing's disease and co-existing phaeochromocytoma

Johnston Philip C , Recinos Pablo , Kennedy Laurence , Hamrahian Amir

Clinical presentation: We report a 46 year old female who presented with a 1 year history of bruising, thin skin and weight gain. In addition; she reported flushing of her chest, heat intolerance, palpitations and abdominal pain. On clinical examination she appeared cushingoid, blood pressure was elevated at 160/98 mm/Hg.Investigations: Biochemical investigations indicated ACTH-dependent Cushing syndrome: 24 h UFC 300 μg (0–50), ACTH 119 pg/ml ...

ea0028p373 | Thyroid | SFEBES2012

Testicular choriocarcinoma: a rare case of thyrotoxicosis arising as a paraneoplastic syndrome

McCracken Emma , Johnston Philip , Lindsay John , Black Neil

An 18 year old male presented with dyspnoea, haemoptysis, weight loss and a large right testicular swelling. On examination he appeared cachectic, diaphoretic and tachycardic. A large firm non-fluctuant right-sided scrotal swelling was present. There were no signs of goitre or dysthyroid eye disease. Thyroid function tests revealed biochemical hyperthyroidism: [fT4 38.6 pmol/L (NR: 9.4–18.6), TSH <0.01 mu/L (NR: 0.3–4.4)]. CT chest demonstrated multiple large pul...

ea0015p81 | Clinical practice/governance and case reports | SFEBES2008

Nasal polyps: an unusual presentation of macroprolactinomas

Johnston Philip , Courtney Hamish , Hunter Steven , Mc Cance David

Intranasal presentations of pituitary tumours are rare. Management can be difficult and delayed due to their location and extension. Macroprolactinomas are uncommon and can often pursue an aggressive clinical course, including invasion into the nasopharynx.We describe three cases of prolactinomas that initially presented to the ENT Department as nasal polyps. Table 1 highlights their clinical features and response to treatment. Recurrence of nasal polyps...

ea0015p100 | Clinical practice/governance and case reports | SFEBES2008

Vasoactive intestinal polypeptide secreting pancreatic tumour (VIPoma) with liver metastases in a 46-year-old male, long term survival after orthotopic liver transplantation

Johnston Philip , Ardill Joy , Johnston Brian , Mc Cance David

A 46-year-old male presented in 1981 with a 2 year history of profuse watery diarrhoea, three stone weight loss and fatigue. On examination he appeared gaunt with diffuse muscle weakness. Investigations revealed hypokalaemia (2.5 mmol/l; NR 3.5–4.5), achlorhydria and a raised vasoactive intestinal polypeptide (VIP) (1500ng/L; NR 0–100). Abdominal CT showed a 5 cm pancreatic mass but with no focal liver pathology. A distal pancreatectomy was performed. Histology confi...

ea0037gp.22.02 | Pituitary–Therapy of Cushing's disease | ECE2015

Surgical outcome and factors associated with Cushing's disease recurrence in 101 consecutive patients operated on by a single pituitary neurosurgeon: the Cleveland Clinic experience

Johnston Philip C , Hamrahian Amir H , Bena Jim , Weil Bob , Kennedy Laurence

Background: Transsphenoidal tumour resection (TSS) is the first-line treatment for Cushing’s disease (CD). With an experienced neurosurgeon, immediate remission rates >80% are expected for patients with microadenomas (<10 mm).Aim: To report initial and long-term remission rates in a specialist centre, and to ascertain factors associated with disease recurrence after TSS.Methods: Patients with CD (n=101, 28M, 7...

ea0037ep748 | Pituitary: clinical | ECE2015

Body weight changes in patients with active Cushing disease after transsphenoidal surgery

Johnston Philip C , Hamrahian Amir H , Weil Robert J , Kennedy Laurence

Background: Successful pituitary surgery in patients with Cushing disease (CD) can result in long term remission and sustained weight loss. We examined rates of body weight changes in the post-operative period (within 6 months) in patients with active CD who underwent transsphenoidal surgery (TSS) and the relationship of weight loss to remission status.Methods: Clinical data was obtained from a CD database in addition to an online patient medical record ...

ea0037ep779 | Pituitary: clinical | ECE2015

The impact of surgical management of Cushing's disease in pregnancy on foetal outcomes

Johnston Philip C , Abbassy Mahmoud , Hamrahian Amir , Kennedy Laurence , Recinos Pablo

Background: Cushing’s disease is a condition rarely encountered during pregnancy. It is known that hypercortisolism is associated with increased maternal and foetal morbidity and mortality.Aims and methods: A comprehensive search of the literature was performed for cases of Cushing’s disease in pregnancy including our own case. Analysis was performed of all pregnant patients with Cushing’s disease who were treated with surgery compared to ...