Searchable abstracts of presentations at key conferences in endocrinology

ea0062we6 | Workshop E: Disorders of the gonads | EU2019

Hormone Replacement Therapy and fertility options in a patient with Premature Ovarian Insufficiency

Almazrouei Raya , Jayasena Channa

Case: A 20 year old female was referred for further evaluation of ovarian function. She has a history of beta thalassemia and bone marrow transplant in 2009 at age 11. Her menarche started in 2008 and she continued having regular periods until shortly after her bone marrow transplant. She was subsequently started on Loestrin oral contraceptive pill. Examination showed a height of 164 cm and weight of 57 kg. She had well developed secondary sexual characteristics. Her OCPs was ...

ea0062we7 | Workshop E: Disorders of the gonads | EU2019

Challenging case of Gonadotropins treatment prior to microdissection testicular sperm extraction (mico-TESE) in patient with Klinefelter syndrome and history of thromboembolism

Almazrouei Raya , Jayasena Channa

Case: A 34 year old was reviewed in reproductive clinic for gonadotropins therapy prior to micro-TESE. He was diagnosed with Klinefelter syndrome in his 20s in another hospital. Testosterone replacement was initiated with Nebido injection. However, he developed polycythemia, DVT and PE in 2013 and therefore the testosterone replacement was stopped. He had thrombophilia screen that showed heterozygous prothrombin gene mutation. Thereafter, he received anticoagulation for few mo...

ea0059p132 | Neuroendocrinology and pituitary | SFEBES2018

Cannulated prolactin is useful to confirm hyperprolactinemia and to minimize inappropriate imaging

Almazrouei Raya , Meeran Karim

Background: Current Endocrine Society guideline recommends a single prolactin level to confirm the diagnosis of hyperprolactinemia. This may lead to over diagnosis and inappropriate imaging. Our institution protocol is to repeat the prolactin and measure macroprolactin. If the second prolactin is elevated, then a cannulated prolactin to role out venipuncture stress effect is undertaken.Methods: Data were collected for 49 patients between January 2017 to ...

ea0059ep86 | Neuroendocrinology and pituitary | SFEBES2018

Sheehan’s syndrome in a man

Almazrouei Raya , Meeran Karim

Background: The blood supply of the pituitary gland comes via a portal circulation from the hypothalamus. During pregnancy, the anterior pituitary gland enlarges but the blood supply cannot increase, as it is derived from a capillary plexus. The pituitary is thus vulnerable to arterial pressure changes and infarction secondary to hypotension. We describe a case of a male patient with large pituitary adenoma who developed Sheehan’s like syndrome due to adenoma infarction s...

ea0062p59 | Poster Presentations | EU2019

Treatment of low bone density with a thiazide-like diuretic in idiopathic hypercalciuria

Almazrouei Raya , Comninos Alex , Cox Jeremy

Case History: A 64 year old lady with osteoporosis was referred for parental antiresorptive therapy due to a history of oral bisphosphonate intolerance. She was screened for osteoporosis at age 53 after her mother suffered a hip fracture, DEXA showing an L2-L4 T score of −2.5 and mean femur −2.2. She was given a trial of alendronate, but stopped due to indigestion. On Calcium and Vitamin D supplementation, the DEXA after 4 years showed improvement of both the spine...

ea0062p63 | Poster Presentations | EU2019

Prednisolone replacement makes steroid optimisation easier in patients on mitotane

Almazrouei Raya , Meeran Karim , Wernig Florian

Case history: A 66 year old lady presented with abdominal pain, new onset diabetes and hypertension. She was diagnosed with Cushing’s syndrome and was found to have a large heterogeneous left adrenal mass of 11.4 × 9.3 cm in size with no disease elsewhere. She underwent a left open adrenalectomy and the histology confirmed an adrenocortical carcinoma (Weiss score of 7) with focal vascular invasion, no extra-capsular spread and clear resection margins. Following surge...

ea0062p66 | Poster Presentations | EU2019

Treatment of low bone density with a thiazide-like diuretic in idiopathic hypercalciuria

Almazrouei Raya , Comninos Alexander , Cox Jeremy

Case History: A 64 year old lady was referred for parental antiresorptive therapy due to a history of oral bisphosphonate intolerance. She had been screened for osteoporosis at age 53 after her mother had suffered a hip fracture, DEXA scan showed an L2-L4 T score of −2.5 and a mean femur −2.2. She was given a trial of alendronate, but had stopped due to indigestion. The DEXA scan at 4 years showed improvement of both the spine and femur densities on Calcium and Vit...

ea0065p11 | Adrenal and Cardiovascular | SFEBES2019

Cosyntropin stimulation test post unilateral adrenalectomy for non-steroid secreting lesions: not all who fail require steroids

Zaman Shamaila , Almazrouei Raya , DiMarco Aimee , Palazzo Fausto , Wernig Florian

Aim: Recent studies reported a wide range in baseline and peak cortisol responses to surgery. We report the results of cosyntropin stimulation testing following unilateral adrenalectomy for non-steroid secreting lesions.Methods: Data of 36 patients who underwent cosyntropin stimulation testing on the second day post unilateral adrenalectomy were collected retrospectively. None of the patients had clinical signs of hypercortisolism. No patient received pr...

ea0062cb8 | Additional Cases | EU2019

Interpretation of bilateral petrosal sinus sampling in Cushing’s disease

Almazrouei Raya , Hatfield Emma , Martin Niamh , Meeran Karim

Case: A 46-year-old woman was initially investigated for right sided intermittent headaches for one year. Her MRI head revealed a pituitary adenoma. She had no history of vomiting with the headache episodes and had no history of visual acuity or field defect. She had amenorrhoea for the past 10 months. Prior to this, she had regular periods following her menarche at the age of 12 years. She admitted to easy bruising but had no hirsutism or acne. She did not report any weight g...

ea0059ep89 | Reproduction | SFEBES2018

From Antipsychotic-related Hyperprolactinemia to Klinefelter Syndrome: Taking the Patient as a Whole

Almazrouei Raya , Ramli Rozana , Hatfield Emma , Meeran Karim , Wernig Florian

A 59 year old man was referred to our endocrine service for persistently elevated prolactin levels. He did not report any headache, visual disturbance or galactorrhoea. He was diagnosed with schizophrenia in 1994 and was tried on different antiphychotic drugs until established on a combination of Amisulpride and Clozapine 11 years later. For the past years, his prolactin levels had been elevated ranging from 1477 to 1972 milliunit/L [60–300]. Further history revealed that...