Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep1292 | Clinical Cases–Thyroid/Other | ECE2015

Clinical case: gender identity disorder as an aetiology of hypothalamic amenorrhoea

Volkova Natalia , Porksheyan Maria , Kanaeva Saida

Hypothalamic amenorrhoea is a diagnosis of exclusion, frequent cause of which are medications or psychiatric disorders (bulimia/anorexia). Here we present a case, when its aetiology was gender identity disorder. A 18-year-old girl presented with absence of menses during last year. Menses began at the age of 14 and were regular till age of 16, when she moved to another city. She was seen by gynaecologist because of amenorrhea, and evaluation was performed: FSH 4.6 mU/ml (1.37&#...

ea0041ep73 | Adrenal cortex (to include Cushing's) | ECE2016

Clinical case of yatrogenic hypercortisolism in pregnant woman with adrenal insufficiency

Volkova Natalya , Porksheyan Mariya , Kanaeva Saida , Davidenko Ilya

Background: Adrenal insufficiency (AI) in pregnant women is difficult to manage because of similarity between clinics of decompensation of AI and gestational toxicosis. Objective difficulty is absence of clinical guidelines of management of pregnant patients with AI. We present a clinical case where the management of pregnant patient was not careful, which led to overdose and iatrogenic hypercortisolism.Clinical case: Pregnant woman, 29years old, asked s...

ea0041ep92 | Adrenal medulla | ECE2016

Clinical case of giant pheochromocytoma with low hormonal activity

Volkova Natalya , Beltsevitch Dmitriy , Porksheyan Mariya , Kanaeva Saida , Davidenko Ilya

Background: Pheochromocytoma (Ph) is the tumor that is fatal if do not suspect and treat it on time. It is supposed that size of tumor is correlated with its synthetic activity. Here we present a clinical case of giant Ph with low synthetic activity that could have been recognized as adrenal cancer, which, in turn, may have led to wrong treatment.Clinical case: Young woman, 28 years old, presented with the adrenal incidentaloma. She had not any complaint...

ea0041ep648 | Endocrine tumours and neoplasia | ECE2016

Clinical case of rare adrenal tumor – schwannoma

Volkova Natalya , Porksheyan Mariya , Kyt Oleg , Kanaeva Saida , Dimitriadi Sergey

Background: Schwannoma (Sch) is a rare peripheral nerve sheath tumor comprised entirely of neoplastic Schwann cells. Adrenal Sch are extremely rare. Most adrenal Sch are incidental, and patients with Sch may not have any complaints. Here we present the clinical case of giant adrenal Sch, which caused hematuria and had indiscriminating organ origin on MRI.Clinical case: Woman, 58 y.o., was consulted by urologist because of painless macrohematuria. Abdomen...