Searchable abstracts of presentations at key conferences in endocrinology

ea0031p111 | Clinical practice/governance and case reports | SFEBES2013

Adrenal incidentalomas: who requires further testing?

Paterson Fiona , Theodoraki Aikaterini , Amajuoyi Adaugo , MacLachlan Jody , Bouloux Pierre , Khoo Bernard

Adrenal incidentalomas are common and guidelines recommend testing to exclude functioning lesions and malignancy. Their increasing prevalence results in a number of investigations usually conducted in the Endocrinology clinic.In 2011 we audited the prevalence and management of adrenal incidentalomas identified on abdominal CT imaging over one calendar month in our centre. Consequently, a decision pathway for new adrenal lesions was introduced in the Radi...

ea0028p67 | Clinical practice/governance and case reports | SFEBES2012

Adrenal incidentalomas outside the Endocrinology clinic

Amajuoyi Adaugo , Theodoraki Aikaterini , MacLachlan Jody , Bouloux Pierre-Marc , Khoo Bernard

Adrenal masses discovered incidentally during imaging (adrenal incidentalomas) are common and constitute a common reason for referral in the Endocrinology clinic. Our aim was to audit the prevalence of adrenal masses discovered in all computerised tomography (CT) abdominal imaging done over one calendar month in our centre. A secondary aim was to identify the underlying diagnosis and fate of the discovered adrenal nodules. All 690 CT scans done in March 2011 in our centre that...

ea0025p105 | Clinical biochemistry | SFEBES2011

Review of 125 individuals with adrenal incidentalomas: a single centre cohort

Theodoraki Aikaterini , Khoo Bernard , Perera Sithara , Schwappach Anna , Hamda Arif , Vanderpump Mark , Bouloux Pierre-Marc

Background: Adrenal masses discovered incidentally during imaging studies (adrenal incidentalomas – AIs) are common and prompt investigations to exclude secretory lesions and malignancy. Uncertainty exists over the best management strategy of AI.Objective: To monitor the current practice against the local protocol and existing guidelines; to identify the biochemical and imaging outcomes in a single centre cohort.Methods: Retro...

ea0022p142 | Cardiovascular endocrinology and lipid metabolism | ECE2010

Insulin mediates the glucagon-induced decrease in atrial natriuretic peptide: a randomized controlled trial

Arafat Ayman , Rudovich Natalia , Adamidou Aikaterini , Spranger Joachim , Weickert Martin , Mohlig Matthias , Pfeiffer Andreas

Objectives: Atrial natriuretic peptide (ANP) is a cardiac hormone that is known to play an essential role in regulation of blood pressure and vascular endothelial function. However, the metabolic regulation of ANP is not fully understood. In patients suffering from metabolic syndrome hypertension, hyperinsulinemia and postprandial hyperglucagonemia are common features. It was the aim of the present study to evaluate the impact of glucagon on proANP and the possible mechanisms ...

ea0022p687 | Obesity | ECE2010

Glucagon stimulates cholecystokinin secretion in humans

Arafat Ayman , Otto Barbel , Adamidou Aikaterini , Spranger Joachim , Weickert Martin , Mohlig Matthias , Pfeiffer Andreas

Objectives: Gastrointestinal hormones are known to modulate satiety. The mechanisms underlying the impact of glucagon on satiety are so far unknown. However, it can be postulated that the glucagon-induced reduction in hunger feeling is mediated through changes in Cholecystokinin (CCK), which is known to play a role in meal termination. It was the aim of the present study to evaluate the impact of glucagon on CCK and the modulation of these effects in obesity.<p class="abst...

ea0094p306 | Adrenal and Cardiovascular | SFEBES2023

The heterogeneous spectrum of adrenal ganglioneuromas: two interesting cases

Ntali Georgia , Kardalas Efstratios , Markou Maria , Mouchtouris Panagiotis , Partsalaki Eirini , Lavrentaki Aikaterini , Kyriakopoulos Georgios , Tzanela Marinella

Introduction: Ganglioneuromas (GNs) are rare, benign tumors, arising from neural crest cells. Their incidence amongst adrenal masses is 0.3%-6%. The majority are incidentalomas and hormonally inactive but a subset may cause compressive effects. Presentation in the context of genetic syndromes (NF1/NF2, RET, MAX, Von Hippel Lindau disease) has been reported. We present two cases of adrenal GNs: Case 1. A 31-year-old female patient who presented with a history o...

ea0063p357 | Thyroid 1 | ECE2019

Association between vitamin D receptor gene polymorphisms and Graves’ disease: a systematic review and meta-analysis

Anagnostis Panagiotis , Veneti Stavroula , Adamidou Fotini , Artzouchaltzi Aikterini-Maria , Boboridis Kostas , Kita Marina

Introduction: The pathogenesis of Graves’ disease (GD) and Graves’ orbitopathy (GO) is not completely understood. On the other hand, vitamin D receptor (VDR) gene polymorphisms have been associated with susceptibility to a variety of chronic autoimmune diseases. The primary aim of this study was to synthesize the best available evidence regarding the association between VDR gene polymorphisms and risk of GD. Secondary aim was to search for their association with GO.<...

ea0090p590 | Calcium and Bone | ECE2023

Post-thyroidectomy development of posterior reversible encephalopathy syndrome (PRES) due to over-replacement of hypocalcemia

Papalou Olga , Katechakis Nikolaos , Koukoula Chrysoula , Beka Aikaterini , Baikousi Dimitra , Gkoufa Kyriaki , Mandrapylia Angeliki , Stratigou Theodora , Vassiliadi Dimitra , Tsagarakis Stylianos

A 61-year-old woman was admitted to the Emergency Department with generalized seizures. She reported general malaise, anorexia, headache and multiple episodes of vomiting that started about 12 h before admission. She had a history of recent thyroidectomy, and she was on oral calcium carbonate (3 gr/day) and alpha calcidol (3 mg/day). Non-contrast head CT scan was negative for major findings. Laboratory work up revealed hypercalcemia (corrected calcium 14,4 mg/dl), renal impair...

ea0049ep859 | Clinical case reports - Pituitary/Adrenal | ECE2017

Hypopituitarism caused by an intrasellar meningioma: case report

Gavriilidou Stavroula , Belis Constantinos , Xydiari Kalliopi , Afentoulidi Aikaterini , Athanasiou Vasilios , Malaktari-Skarantavou Sofia , Tournis Symeon , Savvidis Christos

Meningioma is a common, usually benign, tumor of the brain and the spinal cord that originates from any dura surface. Such lesion accounts for 10 to 15% of nonadenomatous sellar masses. Purely intrasellar meningiomas are relatively rare and can mimic a nonfunctioning adenoma. A 33-year-old man with a history of 1.5 year fatigue, anemia and erectile dysfunction referred to our department. The laboratory data revealed low levels of ACTH, Cortisol, FSH, LH and Testosterone, while...

ea0049ep1202 | Clinical case reports - Thyroid/Others | ECE2017

Follicular variant of papillary thyroid carcinoma with lung, bone, and soft tissue metastases

Belis Constantinos , Gavriilidou Stavroula , Afentoulidi Aikaterini , Xydiari Kalliopi , Athanasiou Vasilios , Malaktari- Skarantavou Sofia , Saranti Sofia , Savvidis Christos

We report on a case of a 63-year-old male patient with a history of metastatic DTC, with both lung and bone metastases and an additional paravertebral mass. The patient presented with enlargement of the left thyroid lobe. FNA was positive for malignancy and subsequent CTs were negative for distant metastases, whereas laboratory tests showed elevated thyroglobulin (Tg>500 ng/ml). The patient underwent total thyroidectomy and the pathology report revealed a multifocal, folli...