Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep1089 | Late Breaking | ECE2023

Influence of muscle mass and strength on bone mineralization with consideration of sclerostin concentration

Patalong-Wojcik Martyna , Sowińska-Przepiera Elżbieta , Malczyk-Matysiak Kinga , Myszka Aleksandra , Janiec Agnieszka , Syrenicz Anhelli

Introduction: Osteoporosis is a disease characterized by a decreased bone strength, as a result of increased bone porosity and impaired mineralization. According to the mechanostat theory, loads generated by the muscle mass and muscle strength, stimulate bone reconstruction.Aim of the study: In our study, we investigated whether muscle strength and mass exert a significant effect on bone mineral density in young adult women. We also tested whether sclero...

ea0067o16 | Oral Presentations | EYES2019

hCG stimulation induces cortisol secretion in menopausal patients with adrenal incidentalomas

Sojat Antoan Stefan , Marina Ljiljana , Ivovic Miomira , Gajic Milina Tancic , Arizanovic Zorana , Lazovic Jelena Milin , Kendereski Aleksandra , Vujovic Svetlana

Introduction: Secretory adrenal tumors sensitive to luteinizing hormone (LH) and/or human chorionic gonadotropin (hCG) are well documented in the literature. LH and hCG share a mutual LH/hCG receptor and a comparable physiological role.Objective: The aim of our study was to evaluate the response of adrenal steroids (cortisol, aldosterone and dehydroepiandrosterone sulphate (DHEAS)) to exogenous hCG stimulation in menopausal patients with adrenal incident...

ea0067gp13 | Poster Presentations | EYES2019

Multiple bilateral lipid-rich adrenal adenomas- how challenging can be a diagnostic process?

Filipowicz Dorota , Cyrańska-Chyrek Ewa , Szczepanek-Parulska Ewelina , Hernik Aleksandra , Klimont Anna , Ruchała Marek

Background: ACTH-Independent Macronodular Adrenal Hyperplasia (AIMAH) is usually manifested as both-sided adrenal incidentalomas with subclinical overproduction of cortisol (<2% of Cushing’s syndrome). The pathogenesis involves genetic factors, expression of adrenal aberrant hormone receptors and paracrine adrenal corticotropin (ACTH) secretion. Treatment is usually bilateral adrenalectomy, but in some cases also unilateral adrenalectomy or pharmacologic therapy can b...

ea0063p325 | Reproductive Endocrinology 1 | ECE2019

Menstrual cycle characteristics in women with premature ovarian insufficiency

Ivovic Miomira , Marina Ljiljana , Tancic-Gajic Milina , Arizanovic Zorana , Stankovic Magdalena , Cirkovic Andja , Kendereski Aleksandra , Vujovic Svetlana

Premature ovarian insufficiency (POI) is characterized by cessation of ovarian function before the age of 40. Variable clinical presentation often postpones the diagnosis. The aim of our study was to assess whether there is a typical menstrual cycles pattern in patients with POI. We have evaluated 101 women, age 36.7±5.78 y. FSH=78.81±37.43 IU/l, E2<50 pg/dl, with confirmed POI referred to our Clinic between 2014 and 2018. Menstrual cycles characteristics were de...

ea0063ep9 | Adrenal and Neuroendocrine Tumours | ECE2019

Singultus persistens as a presentation of addisonian crisis

Pandurevic Srdjan , Marina Ljiljana , Ivovic Miomira , Tancic-Gajic Milina , Arizanovic Zorana , Sojat Antoan Stefan , Kendereski Aleksandra , Vujovic Svetlana

Introduction: It is presumed that hiccups are a vestigial reflex in mammals. They are rather common in healthy subjects. Persistent hiccups (lasting >48 h) are a serious clinical sign, and documented in a number of debilitating conditions. According to the available literature persistent hiccups in Addisonian crisis have been previously documented in only two patients.Case report: In July 2018, a 39 year old man checked into the ER complaining of nau...

ea0049ep1026 | Pituitary - Clinical | ECE2017

Pituitary insufficiency following traumatic thoracic injury in adolescent male patient-case study

Gilis-Januszewska Aleksandra , Wilusz Malgorzata , Turek-Jabrocka Renata , Pantoflinski Jacek , Trofimiuk-Muldner Malgorzata , Kluczynski Lukasz , Hubalewska-Dydejczyk Alicja , Pach Dorota

Traumatic thoracic injuries in children and adolescents are rare, but could be connected with others traumas, often with traumatic brain injury (TBI). Based on data in the current literature, approximately 15–20% of TBI patients develop chronic hypopituitarism. Growth hormone (GH) and ACTH deficiency are the most common, followed by gonadotropins and thyroid-stimulating hormone. The greatest challenge associated with endocrine complications in individuals with polytrauma ...

ea0041ep29 | Adrenal cortex (to include Cushing's) | ECE2016

Long term folow-up of patients with adrenal incidentalomas and subclinical hypercortisolism: a single center experience

Ivovic Miomira , Marina Ljiljana , Tancic-Gajic Milina , Arizanovic Zorana , Milin-Lazovic Jelena , Rakovic Dragana , Stojanovic Zorana , Paunovic Aleksandra , Vujovic Svetlana

It has been more than 70 years since the first adrenal incidentalomas (AI) were described. Most of these tumors are non-secreting, and are found in 4–7% of adult population. Patients with subclinical hypercortisolism (or autonomous cortisol secretion) (SH) are observed in 1–29% of patients with AIs. Evidence suggests that this condition may be associated with higher prevalence of diabetes, obesity, hypertension and osteoporosis.Between 1999 and...

ea0041ep29b | Adrenal cortex (to include Cushing's) | ECE2016

Long term folow-up of patients with adrenal incidentalomas and subclinical hypercortisolism: a single center experience

Ivovic Miomira , Marina Ljiljana , Tancic-Gajic Milina , Arizanovic Zorana , Milin-Lazovic Jelena , Rakovic Dragana , Stojanovic Zorana , Paunovic Aleksandra , Vujovic Svetlana

It has been more than 70 years since the first adrenal incidentalomas (AI) were described. Most of these tumors are non-secreting, and are found in 4–7% of adult population. Patients with subclinical hypercortisolism (or autonomous cortisol secretion) (SH) are observed in 1–29% of patients with AIs. Evidence suggests that this condition may be associated with higher prevalence of diabetes, obesity, hypertension and osteoporosis.Between 1999 and...

ea0041ep300 | Clinical case reports - Pituitary/Adrenal | ECE2016

Temozolomide treatment in pituitary tumor causing Cushing’s Disease resistant to conventional therapy – case report

Gilis-Januszewska Aleksandra , Pantoflinski Jacek , Turek-Jabrocka Renata , Sokolowski Grzegorz , Wilusz Malgorzata , Pach Dorota , Hubalewska-Dydejczyk Alicja

Objective: The management of pituitary tumors causing Cushing’s Disease are a multidisciplinary challenge to clinicians with neurosurgery as a first line treatment followed by the radiotherapy and pharmacotherapy including chemiotherapy.Such tumors are difficult to treat with high rate of recurrence. To date only 25 patients with Cushing Disease treated with the new alkylating agent temozolamide (TMZ) have been reported.Materials and methods: Sixty-...

ea0041ep606 | Endocrine tumours and neoplasia | ECE2016

Novel mutations p.V220E and c.30G>T in menin gene are associated with hereditary predisposition to multiple endocrine neoplasia type 1

Ziemnicka Katarzyna , Budny Bartlomiej , Gut Pawel , Hernik Aleksandra , Leitgeber-Dominiczak Olena , Siudzinski Marcin , Gryczynska Maria , Janicki Adam , Ruchala Marek

Introduction: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant condition characterized by varying combinations of endocrine tumors and commonly accompanying hyperplasia within the parathyroid gland, anterior pituitary and gastrointestinal tract. Heterozygous germline mutation of the tumor suppressor gene MEN1 is the most common cause of the disease. Molecular genetic testing of menin gene, in which mutation is known to cause MEN1 syndrome, detects pathogenic...