Searchable abstracts of presentations at key conferences in endocrinology

ea0056p862 | Pituitary - Clinical | ECE2018

Growth hormone secretion in children treated for medulloblastoma

Kalinin Alexey , Strebkova Natalia , Zheludkova Olga , Kareva Maria

Medulloblastoma is the most common malignant brain tumor in childhood. Treatment of medulloblastoma includes surgery, radiation therapy and chemotherapy. Craniospinal radiation can cause adverse effects on the endocrine system, specifically on the hypothalamic-pituitary axis. Increasing survival rates of pediatric patients with brain tumors lead to increased concern regarding long-term quality of life, including the detection and correction of endocrine disorders. One of the m...

ea0073aep692 | Thyroid | ECE2021

Amiodarone-induced thyrotoxicosis in children: a clinical case

Ivannikova Tatiana , Kalinin Alexey , Strebkova Natalia , Kareva Maria , Bezlepkina Olga

IntroductionAmiodarone is a drug commonly used for the treatment of refractory atrial or ventricular arrhythmias. In 20% of patients, amiodarone may cause subclinical or clinically overt hypothyroidism or hyperthyroidism. The high iodine exposure caused by amiodarone treatment interferes with thyroid autoregulation. Two underlying mechanisms are considered to be involved in the pathogenesis of amiodarone-induced thyrotoxicosis (AIT). AIT1 is more common ...

ea0073aep829 | Late Breaking | ECE2021

Papillary thyroid cancer in adolescents after neuroblastoma in childhood: Description of the two cases

Enikeeva Sofia , Pankratova Maria , Slashchuk Konstantin , Kareva Maria , Peterkova Valentina

BackgroundIt is known that the thyroid gland is sensitive to the damaging effects of irradiation, and patients who have received radiotherapy for tumor treatment require regular thyroid screening subsequently. A few cases of thyroid cancer after receiving 131I-metaiodobenzylguanidine (MIBG) therapy in the treatment of neuroblastoma in childhood have been described (HM van Santen et al 2012; SC Clement et al, 2013). Here, we report the two cases of papill...

ea0085p12 | Bone | BSPED2022

A case series of 8 patients with pseudohypoparathyroidism and variable phenotype

Gubaeva Diliara , Makazan Nadezhda , Kareva Maria , Peterkova Valentina , Ramakrishnan Renuka , Senniappan Senthil

Introduction: Pseudohypoparathyroidism (PHP) is a group of heterogeneous disorders causing parathyroid hormone (PTH) resistance. The features could include Albright’s hereditary osteodystrophy phenotype (AHO) [brachydactyly, short stature, obesity, round face, ectopic ossifications, intellectual disability]. The condition is rare with an estimated prevalence of 0.34-1.1 in 100,000 and the clinical presentation can be variable. Herein, we present 8 patients with PHP from t...

ea0063p1080 | Pituitary and Neuroendocrinology 3 | ECE2019

Impairment of glucose tolerance in children and adolescentstreated for medulloblastoma

Natalia Strebkova , Kalinin Alexey , Vasyukova Olga , Okorokov Pavel , Kareva Maria , Zheludkova Olga

Children and adolescents treated for solid brain tumors with chemotherapy and craniospinal irradiation are at increased risk of metabolic changes development. Current follow-up guidelines for cancer survivors recommend to monitor fasting glucose and HbA1 levels for diabetes/impaired glucose tolerance screening in these patients. The aim of our study was to evaluate metabolic changes in children treated for medulloblastoma with oral glucose tolerance test (OGTT). We examined 63...

ea0049ep345 | Endocrine tumours and neoplasia | ECE2017

Gross CDC73 deletions in young patients with primary hyperparathyroidism in Russia

Mamedova Elizaveta , Mokrysheva Natalya , Vasilyev Evgeny , Voronkova Iya , Orlova Elizaveta , Kareva Maria , Belaya Zhanna , Rozhinskaya Liudmila , Tiulpakov Anatoly

Introduction: Hyperparathyroidism-jaw tumour syndrome (HPT-JT) is a rare disorder, which is frequently characterized by the development of parathyroid carcinomas and atypical parathyroid adenomas and, thus, severe course of primary hyperparathyroidism (PHPT).Case reports: Two patients (1 male and 1 female, 18 y.o. and 13 y.o. at the time of diagnosis of PHPT, respectively) among a cohort of young patients (<40 y.o.) with PHPT, underwent next...

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...