Searchable abstracts of presentations at key conferences in endocrinology

ea0016p112 | Clinical cases | ECE2008

Children with growth retardation due to Rathke cleft cyst

Petrou Vassilios , Papachilleos Petros , Valvis Nikolaos , Ioannidis Dimitrios , Tertipi Athanasia , Georgoulas Thomas , Chadjiathanasiou Charalambos , Papathanasiou Asteroula

Rathke cleft cysts (RCCs) are non-neoplastic sellar lesions derived from remnants of Rathke’s pouch, and mostly asymptomatic. Symptomatic RCCs occur usually in middle-age, are >1 cm, and cause pituitary hypofunction, diabetes insipidus, hyperprolactinemia or visual impairment. In children, RCCs are rare and usually asymptomatic. However, symptomatic cases may present with growth retardation and diabetes insipidus. We report two children with symptomatic RCC manifestin...

ea0016p254 | Diabetes and cardiovascular diseases | ECE2008

Increased serum AGEs is a distinct finding in lean women with PCOS

Diamanti-Kandarakis Evanthia , Katsikis Ilias , Piperi Christina , Kandaraki Eleni , Piouka Athanasia , Papavassiliou Athanasios , Panidis Dimitrios

In insulin resistant, young women with PCOS elevated serum AGEs and their receptor RAGE have been reported. The present study (approved by the local ethical committee) was undertaken to determine whether increased levels of serum AGEs in PCOS is a distinct finding compared with age- and BMI-matched women, presenting the isolated components of the syndrome and whether serum AGE levels were different among PCOS phenotypes. A total of 193 lean non-insulin resistant women were stu...

ea0016p299 | Endocrine tumours | ECE2008

Adrenal ganglioneuroma: a new cause of increased serum calcitonin

Bakola Theodosia , Gkountouvas Anastasios , Aggelopoulou Anastasia , Tertipi Athanasia , Pappas Anastasios , Iakovidou Ioanna , Nisiotis Athanasios , Kaldrimidis Philippos

Introduction: Ganglioneuromas are rare, benign tumors of mature ganglion cells, arising from the sympathetic ganglia and 20% are located in the adrenal medulla, representing 1–4% of adrenal incidentalomas. About 1/3 secrete catecholamines but hypertension and other adrenergic symptoms are rare. About 60% are depicted with 131I- MIBG.Case report: A 72-year-old man was admitted for a left adrenal tumor 9×8 cm, incidentally found in abd...

ea0016p725 | Thyroid | ECE2008

Treatment with thyroxine reduces thyroid volume in euthyroid children with Hashimoto thyroiditis

Scarpa Vasiliki , Kousta Eleni , Tertipi Athanasia , Ioannidis Dimitris , Petrou Vasilis , Chatziathanasiou Charalambos , Papathanasiou Asteroula

Introduction: There is no concensus whether euthyroid children with Hashimoto’s thyroiditis (HT) need treatment with thyroxine.Aim of the study: To assess whether thyroxine influences goitre progression (calculated thyroid volume on U/S scan) in euthyroid children with HT.Subjects and methods: We studied 50 euthyroid children with HT for a 2-year period. Children with a multinodular goitre were not included in the study. Twent...

ea0014p441 | (1) | ECE2007

An 8-year-old boy with seizures and hypokalemia due to a paraganglioma

Petrou Vassilios , George Kolofotis , Georgouli Eleni , Papathanasiou Asteroula , Athanasia Tertipi , Stefanidis Constantinos , Hadjiathanasiou Charalambos

Pheochromocytomas and paragangliomas, tumors originating from the chromaffin cells, are rare in children.We report an 8-year-old boy who was admitted to the intensive care unit with seizures for which the child had to be intubated, severe hypokalemia (1.8 mEq/l), hyponatremia (127 mEq/l) and fever. Parents reported that several months before admission the boy had nocturnal sweating. Brain MRI revealed areas of increased sign intensity in the parietal lob...

ea0081p522 | Adrenal and Cardiovascular Endocrinology | ECE2022

Gastric monomorphic epitheliotropic intestinal T-cell lymphoma with bilateral adrenal metastases

Kaliakatsou Eirini , Markou Athina , Papanastasiou Labrini , Giagourta Irini , Kalantzi Athanasia , Dimitriadi Anastasia , Lenos Michael , Kounadi Theodora , Fountas Athanasios

Introduction: Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL), formerly known as type II enteropathy-associated T-cell lymphoma, is a rare and aggressive subtype of lymphoma of the gastrointestinal track typically noted in Asian or Hispanic populations. Adrenal involvement as part of MEITL is extremely rare. Herein we present a patient of Greek origin with MEITL and bilateral adrenal metastases.Case Presentation: A 74-year-old man presente...

ea0063p91 | Calcium and Bone 1 | ECE2019

Effectiveness of intramuscular Ergocalciferol treatment in a patient with o steomalaciadueto severe vitamin D deficiencyafterbariatric surgery

Papanastasiou Labrini , Gravvanis Christos , Tournis Symeon , Markou Athina , Kalantzi Athanasia , Zoulias Manolis , Georgakopoulou Georgia , Pagoni Stamatina , Kounadi Theodora

Bariatric surgery is a common treatment for morbidly obese patients requiring weight loss and/or metabolic control. Vitamin D (VitD) deficiency and bone loss may occur post-operatively and supplementation with high oral doses of Vitamin D is required. Alternatively, intramuscular depot ergocalciferol (vitamin D2) which slowly releases VitD and overcomes the gastrointestinal tract, could be administrated in such patients.Aim: To present a case of severe V...

ea0041ep251 | Clinical case reports - Pituitary/Adrenal | ECE2016

21-hydroxylase deficiency presenting as bilateral adrenal masses in the sixth decade of life in a phenotypically male but genetically female patient

Panagiotidi Evgenia , Papadakis Georgios , Manitarou Paraskevi , Tzaves Ioannis , Triantafillou Eleni , Kalaitzidou Styliani , Sapera Aggeliki , Katsoulis Konstantinos , Kaltzidou Victoria , Tertipi Athanasia

Introduction: 21-hydroxylase deficiency (21-OHD) is a common inherited disorder accounting for 90–95% of congenital adrenal hyperplasia (CAH) cases. Some cases may be diagnosed in adulthood after the incidental discovery of adrenal masses on computerized tomography (CT).Case report: A 59-year-old male was investigated for incidentally discovered bilateral adrenal masses in an abdomen CT scan, measuring 5 cm on the right and 8 cm on the left adrenal....

ea0037ep846 | Thyroid cancer | ECE2015

Association of calcium-stimulated calcitonin values with pathological findings following total thyroidectomy

Papadakis Georgios , Keramidas Ioannis , Triantafillou Eleni , Kanouta Foteini , Pappa Theodora , Kaltzidou Victoria , Tertipi Athanasia , Vecchini Gino , Papadouli Despoina , Pappas Anastasios

Background and objectives: Medullary thyroid carcinoma (MTC) originates from thyroid C-cells and is a calcitonin (CT) secreting tumour with aggressive behaviour. Surgery is recommended in all patients with basal or calcium-stimulated CT values of 100 pg/ml or higher due to the high probability of MTC. The objective of this study was to investigate the utility of calcium stimulation test for CT in order to distinguish MTC from C-cell Hyperplasia (CCH) preoperatively and to exam...

ea0037ep848 | Thyroid cancer | ECE2015

False-positive uptake of radioiodine WBS in a patient with papillary thyroid cancer due to a vertebral hemangioma

Triantafillou Eleni , Kanouta Foteini , Papadakis Georgios , Tzaves Ioannis , Panagiotidi Evgenia , Trivizaki Erasmia , Kaltzidou Victoria , Tertipi Athanasia , Drosou Aspasia , Pappas Anastasios

Introduction: Diagnostic and post-therapy radioiodine whole body scan (WBS) is used in the follow-up of differentiated thyroid carcinoma (DTC) for the detection of local recurrence or remote metastasis. We report a case of false-positive uptake of radioiodine WBS.Case report: A 37-year-old female patient underwent subtotal thyroidectomy for multinodular goitre and histology revealed multifocal papillary thyroid carcinoma, of follicular type with three fo...