Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep1072 | Thyroid (non-cancer) | ECE2015

Hypothyroidism and the haemodialysis patients: it is a matter for discussion

Aljefery Mohammed

149 haemodialysis chronic renal failure (CRF) patients on haemodialysis (HD) program of 4 h/three times a week investigated for thyroid gland function and try to answer the question: is the thyroid function abnormality affect the response of the haemodialysis CRF patients response to recombinant human erythropoietin (rHuEPO)? We compare the results of the thyroid gland markers; T3, T4, and TSH (which tested by minividus technique) of the patients with the...

ea0016p580 | Paediatric endocrinology | ECE2008

Structural study on the effect of maternal diabetes on fetal endocrine pancreas

Badawoud Mohammed

The effect of maternal diabetes on fetal pancreatic islets was investigated before, however an extensive and detailed quantitative immunocytochemical investigation was not found. Therefore, this investigation was conducted to examine the effect of gestational diabetes on the morphology of fetal rat islets. Sections were stained with anti-insulin (B cells) antibodies and were used for structural study. The absolute number of stained B cells per islet of the diabetic group was n...

ea0081ep82 | Adrenal and Cardiovascular Endocrinology | ECE2022

Glucocorticoids and androgen secreting adrenocortical adenoma: A case report and literature review

Alqahtani Ali , Almehthel Mohammed , Almohaya Mohammed

Background: The presence of Adrenocorticotropic hormone (ACTH)-independent Cushing syndrome that is associated with androgen hypersecretion is extremely rare in benign adrenal tumors. Precise recognition and management of this association will have a great impact on the management of such patient.Clinical case: We describe a case of a 35-year-old lady who presented with 2 years history of difficult-to-control hypertension, symptoms of androgen excess alo...

ea0037ep152 | Reproduction, endocrine disruptors and signalling | ECE2015

Endocrine disruptive effect of plastic byproduct bisphenol A on GH activity

Zadjali Fahad , Al Masroori Mohammed , Habais Mohammed

Bisphenol A (BPA) is a byproduct of polycarbonate plastic widely present in food containers. BPA is historically a known endocrine disruptor and due to its oestrogen agonist activity, BPA consumption is associated with hypothyroidism and reproductive disorder. Recent studies have shown that oestrogen antagonised GH actions. Since BPA has oestrogen agonist activity, the effect of BPA exposure on GH activity has not yet been investigated.Aim: To study the ...

ea0094p47 | Endocrine Cancer and Late Effects | SFEBES2023

In silico-based analysis of differentially expressed miRNAs involved in the ovarian cancer

T. Mohammed Bushra , Taha Mohammed Zainab

Ovarian cancer is one of the major cause of death among women worldwide with high incidence. Ovarian cancer can be categorized into epithelial, non-epithelial (germ cell and sex cord-stromal cell), and metastatic (usually develop from surrounding cancerous organs). Recently, several approaches have been studied to control ovarian cancer at the transcriptional or post-transcriptional levels using small non coding RNAs including microRNAs. We carried out a meta-analysis of previ...

ea0053p05 | (1) | OU2018

Extreme weight loss post-gastric bypass in a recently diagnosed diabetic – the honeymoon trap

Philbey Christopher , Mohammed Kamrudeen

Introduction: Clinicians are hopeful for substantial weight loss after surgical intervention for obesity, with the funding decisions relatively easier to achieve in those with diabetes, there is a significant proportion of these patients undergoing procedures. In contrast to most outpatient encounters, a 20 kg drop in weight is looked upon favourably between follow-ups where it would have risen the spectre of pathology elsewhere. We present the following case that illustrates ...

ea0086p351 | Neuroendocrinology and Pituitary | SFEBES2022

Hypophysis associated with Crohn’s disease - Think DI as well as GI in dehydrated thirsty Crohn’s disease patients with rising sodium!

Jamsheed Mohammed , Bujanova Jana

Introduction: Hypophysitis is a rare association of inflammatory bowel disease (IBD) with only few cases reported in the literature. It can present with isolated hormone deficiencies or panhypopituitarism. Patients may also present with symptoms secondary to inflammatory pituitary mass. Management consists of hormone replacement therapy, but high dose steroids, steroid sparing agents like Rituximab or even surgery may be required for mass effect.Case rep...

ea0086p147 | Thyroid | SFEBES2022

An Unusual Presentation of An Autoimmune thyroid Disease

Alkaabi Fatima , Ismail Mohammed

40years old lady with 12 months history of hyperthyroidism. Treated with ATD. Referred by her treating physician for RAI therapy due to intolerance to ATD and high dose requirement after 12 months. Patient being treated as Classical Graves’ Hyperthyroidism. She had symptoms of hyperthyroidism at time of presentation but none at time of assessment in our hospital. Main current issue was painful neck swelling: developed slowly over preceding two months. No problems with swa...

ea0091wd12 | Workshop D: Disorders of the adrenal gland | SFEEU2023

Primary bilateral macronodular adrenal hyperplasia as a cause for Cushing syndrome

Shamsaldeen Mohammed , Panicker Janki

Introduction: Primary bilateral macronodular adrenal hyperplasia (PBMAH) is a rare cause of Cushing’s syndrome and is more often diagnosed as bilateral adrenal incidentalomas with subclinical cortisol production. It is mainly a heterogeneous disease, but familial cases have been reported. Treatment of PBMAH with overt Cushing’s syndrome is usually bilateral adrenalectomy with unilateral adrenalectomy occasionally used to normalize urinary free cortisol (UFC) in patie...

ea0091cb14 | Additional Cases | SFEEU2023

Familial dysalbuminemic hyperthyroxinemia (FDH)

Shamsaldeen Mohammed , Panicker Janki

Introduction: Familial dysalbuminemic hyperthyroxinemia (FDH) is a familial autosomal dominant condition that was first reported in 1979. It is caused by a mutant albumin molecule with an increased affinity for serum thyroxine (T4), despite the serum albumin level being normal. FDH causes increase in total T4 and T3 level with normal TSH level. As FDH patients are clinically euthyroid and asymptomatic, they do not require treatment.Case report: 68-year-o...