Searchable abstracts of presentations at key conferences in endocrinology

ea0070ep323 | Pituitary and Neuroendocrinology | ECE2020

Association of an empty sella and grave’s disease in a patient with acromegaly

Halloul Imen , Abdelkarim Mzoughi Asma Ben , Slim Ahlem , Saad Ghada , Othman Wafa Ben , Hasni Yosra , Maaroufi Amel , Kacem Njah Maha , Chaieb Molka , Ach Koussay

Introduction: Acromegaly is, in most cases, caused by growth hormone (GH) -secreting pituitary adenomas that lead to characteristic phenotypical changes. Its association with emty sella (ES) has been described and different theories has been given to explain such situation. Moreover, patients with acromegaly often develops different pathologies of the thyroid gland, however, the occurrence of grave’s disease (GD) is quite a rare situation. Here we report a case of a pati...

ea0070ep366 | Pituitary and Neuroendocrinology | ECE2020

Recurrent cushing’s disease and pregnancy: A case report

Benothman Wafa , Saad Ghada , Halloul Imen , Ben Abdelkrim Asma , Hasni Yosra , Chaeib Molka , Kacem Maha , Maaroufi Amel , Ach Koussay

Introduction: Cushing’s disease (CD) is reported in 60-70% of all patients with Cushing’s syndrome (CS), but occurs only in approximately 33% of the reported CS cases in pregnancy. Nevertheless, despite its rarity, pregnancy in patients with CS can be troublesome because of the risk of maternal-fetal complications.Observation: A 28-year-old female patient was referred to our endocrinology department for a suspected CS with morphological alter...

ea0070ep585 | Hot topics (including COVID-19) | ECE2020

Alopecia universalis as clinical manifestation of hashimoto’s thyroiditis: A case report

Dian Hidayah Canggih , Tahapary Dicky , Harbuwono Dante

Background: Thyroid hormone has an important role for skin growth and development. Alopecia is one of the clinical feature of autoimmune hypothyroidism or systemic autoimmune diseaseCase IllustrationA 18-year-old Indonesian woman presented with alopecia universalis. It started with a patchy hair loss which then progress to all of her body. At the age of 15 she had complaints of neck enlargement, palpitation, weight loss, and heat i...

ea0014oc8.7 | Neuroendocrinology clinical | ECE2007

A single intravenous bolus of dexamethasone for the diagnosis of Cushing’s syndrome

Munter Gabriel , Kirshner Moriah , Ariel Rosler , Shmuel Shilo , Gil Leibowitz , Benjamin Glaser

The diagnosis of Cushing’s syndrome (CS) is based primarily on diagnostic tests evaluating the cortisol response to dexamethasone suppression. Tests based on oral administration of dexamethasone may be compromised by poor compliance. We evaluated the diagnostic accuracy of a novel intravenous dexamethasone suppression test (IDST). The test is performed by intravenous (iv) bolus injection of 8 mg dexamethasone, with blood cortisol determinations made before injection, then...

ea0014p510 | (1) | ECE2007

The assesment of life quality satisfaction in women with Turner’s syndrome

Wikiera Beata , Szpich Elzbieta , Barg Ewa , Noczynska Anna

Quality life satisfaction is important for personal resources analysis and perspectives for coping with ilness.The aim of the study was to present a psychological portrait of a woman with Turner’s syndrome (TS) and assessing perspectives for increased well-being of such patients. The study concerns psychological aspects of TS women’s own assessment of their health and illness.The area of interest was:<p class="...

ea0013p248 | Neuroendocrinology and behaviour (including pituitary) | SFEBES2007

RNA interference as a therapy for a model of Cushing’s disease

Munir Alia , Eltobgi AbdulAdim , Abbott Lee , Newell-Price John

Introduction: Pro-opiomelanocortin (POMC) is a precursor polypeptide which is cleaved to make adrenocorticotrophic hormone (ACTH) in the anterior pituitary. It is activated in Cushing’s disease. Current therapies for Cushing’s disease are inadequate. RNA interference (RNAi) allows highly specific and effective suppression of gene expression by use of short interfering RNAs (siRNAs).Method: In the current study we employed custom designed siRNAs...

ea0013p266 | Steroids | SFEBES2007

A case of Addison’s disease associated with hypogonadotrophic hypogonadism

Zachariah Sunil , Hyer Steve

A 30 year old gentleman was admitted to our department with symptoms of tiredness and weight loss over the past 3 weeks. He also gave a history of erectile dysfunction for several years. His only significant past history was asthma well controlled on inhalers. On examination he appeared tanned. There was no buccal or skin crease pigmentation. Smell sensation was normal and he had normal external genitalia and secondary sexual characteristics.Initial inve...

ea0013p311 | Thyroid | SFEBES2007

A case of Burkitt’s lymphoma of the thyroid presenting as myxoedema coma

Ibrahim Ibrahim M , parr John , Pritchet Christopher , Wahid Shahid

Introduction: Myxoedmea coma is an extreme expression of hypothyroidism with a high mortality rate. It is rarely associated with thyroid lymphoma.Case report: A 66-year-old lady presented acutely unwell with a two week history of cough and shortness of breath. She was hypothermic, hypoxic with clinical and radiological signs of pneumonia. Her TSH was 99.8 mU/L and T4 less than 5 pmol/L with strongly positive thyroid microsomal antibodies, raised WBC and ...

ea0011p119 | Clinical case reports | ECE2006

Cushing’s syndrome in an adolescent with MEN1: where is the lesion?

Smeeton F , Davies JS , Scanlon MF , Rees DA

A 14 year old girl, with a family history of MEN1, presented with secondary amenorrhoea and weight gain. Biochemical investigation revealed raised 24-hour urinary free cortisol excretions (1455, 1190, 614 nmol/24 hours; normal <290) and failure of cortisol suppression following 48 hours of low dose (0.5 mg qds) dexamethasone (199 nmol/l to 202 nmol/l). High dose dexamethasone administration (2 mg qds) for 48 hours resulted in further suppression of serum cortisol to 49 nmo...

ea0011p172 | Clinical case reports | ECE2006

Addison’s disease: Soy Sauce – a lifesaving concoction

Bhattacharya B , Ullah A , Smellie WSA , McCulloch A , Heald AH

Background: Before synthetic cortisone was introduced, patients with Addison’s disease prolonged their lives by maintaining a high salt intake and taking plant based containing preparations affecting steroid metabolism. We report the case of someone who discovered this regime for herself.Case report: A 42 year old lady presented with a four week history of decreased energy, malaise, and postural dizziness. She was hyponatraemic (plasma sodium 126 mm...