Searchable abstracts of presentations at key conferences in endocrinology

ea0022p67 | Bone/Calcium | ECE2010

Estimation of ionized calcium levels after thyroidectomy at King Abdul Aziz University Hospital (Jeddah)

Qari Faiza

Aim: To determine the incidence of hypocalcaemia and the need for calcium supplementation after thyroid surgery in 120 patients.Methods: A prospective study to determine the incidence of hypocalcaemia by measuring ionized calcium level in 120 patients underwent thyroidectomy at King Abdul Aziz University Hospital, the data included pre- and post-operative ionized calcium level, albumin, free thyroxine, thyrotopin and alkaline phosphatase. As well include...

ea0094p333 | Bone and Calcium | SFEBES2023

An unusual case of refractory hypocalcaemia

Coco Mohamed , Sheikh Katrina , Shakher Jayadave , Osman Basheir

Authors: Mohamed Coco, Katrina Sheikh, Basheir Osman, Jayadave Shakher: Department of Acute Internal Medicine, Birmingham Heartlands Hospital-University Hospitals BirminghamIntroduction: Although skeletal metastatic diseases have commonly been associated with hypercalcemia; we present a case of severe hypercalcemia secondary to extensive skeletal sclerotic metastatic disease.Case: ...

ea0090p541 | Late-Breaking | ECE2023

In silico approaches advocates the sensitivity of adrenal gland against EDCs shown in male Wistar rats

Ahmad Shahzad , Raisuddin Sheikh

Adrenal gland is a less focused endocrine organ for the endocrine disrupting effect of endocrine disrupting chemicals (EDCs). The effects of two extensively used phthalate esters viz. di-ethyl hexyl phthalate (DEHP) and di-butyl phthalate (DBP) on adrenal gland were observed in Wistar rats in the present study to check the susceptibility of adrenal gland against the exposure of these extensively used plasticizers which are well known EDCs. Wistar rats were divided into seven g...

ea0091cb30 | Additional Cases | SFEEU2023

A presentation of Graves’ thyrotoxicosis

Sheikh Abdur-Raoof

A female patient in her early forties was referred to the endocrine clinic. She initially presented to her general practitioner with symptoms of leg cramps and feeling lethargic. As part of initial investigation, thyroid function tests were performed which revealed Free T4 >100 pmol/lwith a TSH suppressed <0.02mU/l. She was promptly commenced on carbimazole for thyrotoxicosis. On retrospective questioning, there was history of weight loss greater than one stone, over t...

ea0070oc8.3 | Environmental Endocrinology | ECE2020

Comparative histopathology of endocrine glands in phthalate exposed male Wistar rats unveil the vulnerability of adrenal gland and augmented by molecular docking

Ahmad Shahzad , Raisuddin Sheikh

Limited research has been conducted on adrenal gland as target of endocrine disrupting chemicals (EDCs). Moreover, studies on steroidogenesis as the target of EDCs has also attracted lesser attention compared to other metabolic pathways. We studied the effects of two extensively used phthalate esters viz., di-ethyl hexyl phthalate (DEHP) and di-butyl phthalate (DBP) on the adrenal gland in Wistar rats and checked its susceptibility against the exposure of these extensively use...

ea0099ep929 | Adrenal and Cardiovascular Endocrinology | ECE2024

Angiomyolipoma of right adrenal gland

Ahmed Mariyah , Shaikh Sheeba , Gulamhusein Aziz , Oliveira Pedro , Adam Safwaan

We describe the case of a 52-year-old female, with a body mass index of 32 kg/m2 and without significant co-morbid illness who initially presented acutely, with self-resolving abdominal pain. During that admission, an abdominal computed tomography (CT) scan demonstrated a right-sided heterogeneous and contrast enhancing adrenal mass (measuring 59×41 mm) with a 15 mm focus of cystic degeneration. Based on the scan appearances, the patient was suspected as having...

ea0026p603 | Clinical case reports | ECE2011

Unusual case of congenital adrenal hyperplasia: polymenorrhagia and markedly high 17-OH progesterone levels in a lady with non classic congenital adrenal hyperplasia

Rizwan A , Hayat M , Sheikh Z

Introduction: Congenital adrenal hyperplasia (CAH) due to 21 hydroxylase deficiency is one of the most common autosomal recessive hereditary diseases. There are two main forms of CAH: early onset, the classic variety, and late onset or non classic type. Here, we aim to describe the case of a young lady with features of both varieties of CAH.Case report: Twenty-three-year-lady of Asian descent presented with polymenorrhagia since menarche (age 13 years), ...

ea0026p604 | Clinical case reports | ECE2011

Schmidt’s syndrome: unveiling step-by-step

Rizwan A , Hayat M , Sheikh Z

Introduction: Autoimmune polyendocrine syndrome type II (APSII) is more common than APSI. It occurs more frequently in female than in male patients, often has its onset in adulthood, and has familial aggregation. Schmidt’s syndrome is a subset of APSII, usually associated with primary hypothyroidism, primary adrenal insufficiency, and often, type 1 diabetes. This case describes the interesting evolution of autoimmune polyendocrine disease (APED) in a young lady with long ...

ea0073aep414 | General Endocrinology | ECE2021

Menopausal hormone therapy and women’s health: an umbrella review of systematic reviews and meta-analyses of randomized controlled trials and observational epidemiological studies

Guo-Qiang Zhang , Jin-Liang Chen , Luo Ying , Mathur Maya B. , Anagnostis Panagiotis , Nurmatov Ulugbek , Talibov Madar , Zhang Jing , Hawrylowicz Catherine M. , Lumsden Mary Ann , Critchley Hilary , Sheikh Aziz , Bo Lundbäck , Cecilia Lässer , Kankaanranta Hannu , Lee Siew Hwa , Nwaru Bright I.

ImportanceThere remains uncertainty about the impact of menopausal hormone therapy (MHT) on women’s health. A systematic, comprehensive assessment of the effects on multiple outcomes is lacking.ObjectiveTo comprehensively summarize evidence on the benefits and harms of MHT across diverse health outcomes in women.Data sourcesMEDLINE, EMBASE and 10 other databa...

ea0090ep1135 | Late Breaking | ECE2023

Doege-Potter Syndrome, cause of paraneoplastic hypoglycaemia in a patient with a Solitary Fibrous Tumour: A Case Report

Sheikh Anum , Calvo Latorre Julia , Kehinde Razak

Background: Non-islet-cell tumour hypoglycaemia (NICTH) is a rare paraneoplastic syndrome caused by an extra pancreatic tumour(1). Solitary fibrous tumour (SFT), amongst other tumours, is one of the rare causes of NICTH. We report a case of NICTH who presented with recurrent hypoglycaemias and was identified to have a fibrous tumour as part of the work up for his symptomatic hypoglycaemias.Case Summary: A 75-year male had presented to the emergency depar...