Searchable abstracts of presentations at key conferences in endocrinology

ea0032p238 | Clinical case reports – Pituitary/Adrenal | ECE2013

Craniofacial fibrous dysplasia and pituitary gigantism in a 10-year-old boy: clinical case

Gusova Anna , Mazerkina Nadezhda

Introduction: The combination of poly/monostotis fibrous dysplasia, café-au-lait pigmentation of the skin and endocrine hyperfunction (mostly precocious puberty) is known as McCune–Albright syndrome (MAS), a genetic origin syndrome with low incidence. The molecular basis of MAS is a mosaic activating mutation of the α subunit of the G protein (Gsα) gene.We present a clinical case of a 10-year-old boy with partial MAS and GH-secreting ...

ea0035p187 | Cardiovascular Endocrinology & Lipid Metabolism | ECE2014

Metabolic outcomes in childhood cancer survivors

Tselovalnikova Tatiana , Pavlova Maria , Zilov Alexey , Mazerkina Nadezhda , Zheludkova Olga

Aim: The aim of this study was to evaluate metabolic abnormalities in young adults getting treatments of acute lymphoblastic leukemia (ALL) and brain tumors (BT) in their childhood.Methods: We examined 50 patients in two groups. The group-1: 18 ALL-survivors (nine women and nine men). All of them received cranial irradiation in dose up to 18 Gy and chemotherapy. In group-2: 32 BT-survivors (14 women and 18 men) were included. All patients received cranio...

ea0034p183 | Neoplasia, cancer and late effects | SFEBES2014

Long-term negative effects in young cancer survivors: metabolic disorders in the patients after complex treatment for brain tumors and acute lymphoblastic leukemia in childhood and adolescence

Tselovalnikova Tatiana , Pavlova Maria , Zilov Alexey , Mazerkina Nadezhda , Zheludkova Olga

Aim: The aim of this study was to examine the incidence of metabolic abnormalities in adults getting treatments of brain tumors (BT) and acute lymphoblastic leukemia (ALL) in their childhood or adolescence.Methods: patients were divided in two groups. In group 1: 31 BT survivors (13 women and 18 men) were included. All patients received craniospinal irradiation up to 36 Gy and boost to the tumor up to 55 Gy and chemotherapy. The group 2: 18 ALL survivors...

ea0032p704 | Neuroendocrinology | ECE2013

Evaluation of GH deficiency and central adrenal insufficiency in patients following craniospinal irradiation in young ages: comparison between the glucagon stimulation test and the insulin tolerance test

Yudina Alla , Tselovalnikova Tatiana , Pavlova Maria , Mazerkina Nadezhda

The patients following craniospinal irradiation (CSI) in young ages due to posterior fossa tumors had high risk of hypopituitarism. The glucagon stimulation test (GST) may be used as alternative the insulin tolerance test (ITT) in the diagnosis of GH deficiency (GHD) and central adrenal insufficiency (CAI) when insulin-induced hypoglycaemia is contraindicated e.g. history of convulsions, coronary heart disease, also it can be carry out as an outpatient. The aim of this study w...

ea0063p1051 | Pituitary and Neuroendocrinology 3 | ECE2019

A comparison of glucagon stimulation and insulin tolerance test in young adults followed craniospinal irradiation

Yudina Alla , Pavlova Maria , Sotnikov Vladimir , Mazerkina Nadezhda , Zheludkova Olga , Martynova Evgeniya

The glucagon stimulation test (GST) may be used as a good alternative to the insulin tolerance test (ITT) in the diagnosis of secondary adrenal insufficiency (SAI). The aim of the study was to compare the GST and ITT for diagnostic SAI, to define cortisol cut-off points and factors affecting the appearance of false positive results in young adults followed CSI.Subjects and Methods: A retrospective study of 28 patients (median age 19 [17; 23]) at least 2 ...

ea0049ep1057 | Pituitary - Clinical | ECE2017

DHEA-S as a marker of the secondary adrenal insufficiency following craniospinal irradiation

Yudina Alla , Pavlova Maria , Tselovalnikova Tatiana , Mazerkina Nadezhda , Arefyeva Irina , Gheludcova Olga

Abstract: The secondary adrenal insufficiency (SAI) is life-threatening disease. 30–50% of patients have SAI following craniospinal irradiation (CSI). The “gold standard” of SAI diagnosis is the insulin tolerance test but it is demanding for patient and medical staff. The simple and reliable test would allow to use ITT rarely. The aim was to evaluate probability of using DHEA-S in SAI diagnosis. 41 patient after CSI non-pituitary brain tumors survivor and 23 hea...

ea0041ep752 | Neuroendocrinology | ECE2016

The hypotalamic-pituitary-adrenal axis changes in non-pituitary brain tumors survives and the best method of its diagnostic

Yudina Alla , Tselovalnikova Tatiana , Pavlova Maria , Mazerkina Nadezhda , Gheludcova Olga , Arefeva Irina , Martynova Evgenia , Koklina Anastasia

The number of the non-pituitary brain tumors survives increases and will be growing up in the future. Although the prevalence of secondary adrenal insufficiency (SAI) vary depending on the methods of diagnostic, we have a few data about their ACTH and DHAE-S status. The aim of our study was to describe the hypotalamic-pituitary-adrenal axis (HPAA) changes after craniospinal irradiation (CRT) and diagnostic utility basal cortisol (BC), DHAE-S, glucagon stimulation test (GST) in...

ea0049ep1025 | Pituitary - Clinical | ECE2017

A novel DICER1 gene mutation in a 10-month-old boy presenting with ACTH-secreting pituitary blastoma and lung cystic dysplasia

Kalinin Alexey , Strebkova Natalia , Tiulpakov Anatoly , Vasiliev Eugene , Petrov Vasily , Kolodkina Anna , Kareva Maria , Mazerkina Nadezhda , Peterkova Valentina

Hypercortisolism due to Cushing disease is an extremely rare condition in children under one year of age. We present a case of a 10-month-old boy with lung cystic dysplasia and pituitary blastoma (ACTH-secreting). The disease manifested with symptoms of hydrothorax due to cystic dysplasia of the right lung’s upper lobe. Surgical resection of the affected area has been carried out. Symptoms of endogenous hypercortisolism appeared soon after lung surgery. Cushing disease du...

ea0056p843 | Pituitary - Clinical | ECE2018

Combined treatment of craniopharyngiomas

Kutin Maxim , Konovalov Aleksander , Kadashev Boris , Astafyeva Liudmila , Serova Nataliya , Kalinin Pavel , Fomichev Dmitriy , Mazerkina Nadezhda , Sidneva Yuliya , Trunin Yrii

Introduction: Craniopharyngiomas (CF)- benign epithelial tumors that develop from the remnants of Rathke’s pouch cells. Most often, CF manifest themselves in two age groups: in children 5–14 years old making 5.6–13% of intracranial tumors and in adults 50–74 years old making 2–5%.Materials and methods: In the last decade, the Institute annually for the surgical treatment received 100–120 patients with CF. The total number of...