Searchable abstracts of presentations at key conferences in endocrinology

ea0070aep502 | Diabetes, Obesity, Metabolism and Nutrition | ECE2020

Different short-term responses of image dissatisfaction and distortion to sleeve gastrectomy

Naliato Erika

Introduction: Bariatric surgery is one of the most important treatment modalities for obesity. Studies suggested that obese subjects have distorted body image perception. Dissatisfaction with body shape is one of the leading reasons for treatment referral.Aim: To prospectively study body image perception and its relationship with body composition in patients treated with bariatric surgery.Methods: Nineteen patients were evaluated b...

ea0070ep171 | Diabetes, Obesity, Metabolism and Nutrition | ECE2020

Gender differences in image dissatisfaction and distortion in brazilian patients referred to bariatric surgery

Naliato Erika

Introduction: In Brazil, most patients referred to bariatric surgery are women. The literature indicates the occurrence of gender differences in body composition and body image perception.Aim: To study body image perception and its relationship with body composition in Brazilian bariatric patients.Methods: A total of 140 patients were evaluated using the Stunkard Figure Rating Scale (SFRS) and bioimpedance. Image dissatisfaction an...

ea0049ep152 | Endocrine tumours and neoplasia | ECE2017

Incidental paraganglioma, diagnosis and follow-up – case report

Violante Alice , Lemme Roberto , Galvao Sarah , Naliato Erika

Paragangliomas and Pheochromocytomas are tumors originated from chromaffin cells (Pheochromocytomas (PHEO): adrenal glands; Paragangliomas (PGL):paravertebral thoracic, abdominal, and/or pelvic sympathetic ganglia, and glossopharyngeal and vagal neck and skull base parasympathetic ganglia). Catecholamine hypersecretion predominates in PHEO, while PGL are oligosymptomatic with compression-related symptoms. The authors report the case of a 33-year-old male with an incidental ret...

ea0073ep151 | Pituitary and Neuroendocrinology | ECE2021

Fasting glucose and other metabolic features of 17 Brazilian women with microprolactinomas

Botelho Mariana , Sousa Rafaela , João Nascimento , Lamounier Filho Adilson , Naliato Erika , Violante Alice

IntroductionAmong other organic functions, Prolactin (PRL) can influence metabolism.AimTo evaluate basal glucose metabolism in women with prolactinoma, according to menstrual cycle, presence of hyperprolactinemia, and dopamine agonist (DA) treatment.Material and methodsCross-sectional study of 17 women with microprolactinoma and 11 healthy controls. Variables eval...

ea0070aep26 | Adrenal and Cardiovascular Endocrinology | ECE2020

Genetic alterations and clinical features in 16 brazilian patients with pheochromocytomas and paragangliomas

Naliato Erika , Araujo Paula , Soares Paula , Lima Jorge , Lima Vinicius , Wo Julia , Sanchez Mirna , Carvalho Denise , Violante Alice

Introduction: Pheochromocytomasand paragangliomas are tumors derived from chromaffin cells which result from mutations of at least six different genes as autosomal dominant disorders.Aim: To evaluate the existence of correlations between genetic alterations and clinical data in 16 patients with pheochromocytomas and/or paragangliomas.Methods: From 2007 to 2009, 13 patients with pheochromocytoma [3 men, medium age 39 years (14&#8211...

ea0056ep12 | Adrenal and Neuroendocrine Tumours | ECE2018

The changing of clinical scenario in three consecutive generations of a Brazilian Family with Von Hippel-Lindau disease

Violante Alice , Lima Jorge , Soares Paula , Macedo Ana , Neto Silvio Cunha , Naliato Erika , Migowski Joao , Alecrim Amanda , Lima Vinicius , Carvalho Denise , Lourenco Delmar

Background: Von Hippel Lindau Disease (VHL) is an autosomal dominant inherited syndrome characterized by high susceptibility to the development of a wide spectrum of benign and malignant, endocrine and non-endocrine neoplasias in diverse organs of patients harboring a germline mutation in VHL tumor suppressor gene. The major clinical manifestations of VHL are brain, cerebellar and spinal cord hemangioblastoma, retinal angioma, pheochromocytoma, renal cell carcinoma an...

ea0081p146 | Pituitary and Neuroendocrinology | ECE2022

Central Diabetes Insipidus, family report, molecular study, and its importance

Filipe Sa Luis , Sousa Rafaela , Villela Darine , Cavalcanti Thereza , Migliavacca Michele , Fontes Rosita , Guimaraes Marilia , Souza Micheline , Coelho Paula , Botelho Mariana , Nascimento Joao , Carvallo Mirna , Viveiros Pedro , Lourenco Jr Delmar , Naliato Erika , Violante Alice

Introduction: Central diabetes insipidus (CDI) occurs due to deficient secretion of arginine vasopressin (AVP) or antidiuretic hormone (ADH) by the posterior pituitary. It is a rare disease with an estimated prevalence of 1:25000. CDI can be acquired or congenital, secondary to malformation or genetics. Familial CDI (genetic inheritance) is mainly autosomal dominant. More than 80 mutations in the AVP gene have been described. In hereditary CDI, the age of onset is variable. Sy...