Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep996 | Thyroid | ECE2023

A case report: non-germinal center type diffuse large B-cell lymphoma in thyroid

Kriksciuniene Ruta , Siusaite Gabija , Klimaite Raimonda

Introduction: The diffuse large B-cell lymphoma (DLBCL) is known as one of the most common lymphoma worldwide with the prevalence of 25 % of all of non-Hodgkin lymphoma cases [1], but it is very rearly observed in thyroid. Around 30 % of Clinical cases of the DLBCL appear from extranodal organs, the prognosis depends on the site of origin [2].Case: A 18-year-old man was admitted to endocrinologist, complaining with a palpable nodule in the front neck for...

ea0056p323 | Clinical case reports - Thyroid/Others | ECE2018

Maturity – onset diabetes in the young and non-alcoholic fatty liver disease: a case report

Kadusauskiene Agne , Klimaite Raimonda , Jakuboniene Neli

Introduction: Maturity-onset diabetes of the young (MODY) is a form of diabetes mellitus transmitted by an autosomal dominant mode of inheritance, usually diagnosed before the age of 25 years. Non-alcoholic fatty liver disease (NAFLD) is a chronic liver disease, particularly closely related with insulin resistance and type 2 diabetes mellitus. MODY and NAFLD combination has rarely been described in the literature.Case: A 25-year-old women was admitted to...

ea0056p995 | Clinical case reports - Thyroid/Others | ECE2018

Coexistence of hashimoto thyroiditis and De Quervain’s thyroiditis

Klimaite Raimonda , Banisauskaite Ilona , Valickas Raimondas

Introduction: De Quervain’s Thyroiditis (DQT) is a self-restriction inflammatory disease of the thyroid gland that presents severe pain localized in the neck. But few cases of a painful variant of Hashimoto’s thyroiditis (HT) have been described as well. Thyroid ultrasound (US) may reveal in homogeneous hypoechoic pattern in both conditions.Case: A 51-year old woman was admitted to the Hospital of Lithuanian University of Health Sciences, Kauno...

ea0090ep1078 | Thyroid | ECE2023

Clinical case: I131 resistant follicular thyroid carcinoma

Siusaite Gabija , Kairyte Beata , Klimaite Raimonda , Zilaitiene Birute

Introduction: Follicular thyroid carcinoma (FTC) is the second most common thyroid tumor and accounts for about 5-10 % of all thyroid cancers. As FTC often retains the ability to concentrate radioactive iodine (I131), tumor may be responsive to I131 therapy. However, about 60-70 % of all metastatic thyroid cancers are resistant to I131 and has a poor prognosis with 10-year survival rate of 10 % and the average life expectancy 3-5 years after di...

ea0063p404 | Thyroid 1 | ECE2019

Pancytopenia and reversible cardiomyopathy - complications of thyrotoxicosis: case report

Klimaite Raimonda , Kinderyte Marija , Dauksaite Neda , Barsiene Lina , Zilaitiene Birute

Introduction: Grave’s disease is frequently associated with cytopenia. Pancytopenia, however, is rare. Thyroid hormones have a direct effect on myocardial contractility and left ventricle (LV) diastolic function. Only less than 1% of the patients with hyperthyroidism develop cardiomyopathy with impaired left ventricular systolic function.Case: A 51-year old woman was admitted to the Hospital of Lithuanian University of Health Sciences, Kaunas clinic...

ea0049ep1321 | Thyroid (non-cancer) | ECE2017

Hashimoto Encephalopathy with polymorphic neuropsychiatric signs: a case report

Simoniene Diana , Klimaite Raimonda , Mikelaityte Greta , Danyte Evalda

Hashimoto encephalopathy (HE) is a rare and steroid responsive encephalopathy associated with autoimmune thyroiditis (1). Patients with Hashimoto encephalopathy may present with a variety of neuropsychiatric signs (2). 68-year old woman was admitted to the Neurology Department, of Hospital of Lithuanian University of Health Sciences, Kauno klinikos (HLUHS KK), due to disorder of consciousness of uncertain aetiology in August 2016. The signs of motor dysfunction, generalized ri...

ea0049ep1436 | Thyroid (non-cancer) | ECE2017

Massive thyroid gland metastasis from nonsmall cell lung cancer

Simoniene Diana , Daneliene Milda , Klimaite Raimonda , Mikalauskaite Rasa

Despite that the thyroid gland is one of the most vascular organs of the body but thyroid gland is an uncommon site for metastasis [1]. It represents less than 4% of thyroid malignancy in clinical and surgical studies [2, 3]. 58-year-old male, a prior smoker, was diagnosed with nonsmall cell lung cancer T4N3M1 St IV, histopathological findings - infiltrative adenocarcinoma, G1. About eight months he was treated with chemotherapy. At the beginning of the disease, the patient wa...

ea0041ep124 | Bone & Osteoporosis | ECE2016

Bone mineralization and hormonal status in Turner syndrome patients: cross sectional one population study

Klimaite Raimonda , Kriksciuniene Ruta , Zilaitiene Birute , Verkauskiene Rasa

Introduction: Women with Turner syndrome (TS) are known to be at risk of decreased BMD (dBMD). Sex hormone replacement therapy is crucial to ensure the proper BMD formation, although the dBMD remains a problem in TS.Aim: To investigate the prevalence of decreased bone mineralization and it’s association with hormone levels in TS.Subjects: Women with geneticaly confirmed TS aged ≥ 18 year.Methods: T...

ea0070ep59 | Bone and Calcium | ECE2020

Extremely rare and slow-progressive parathyroid carcinoma: Case report

Klimaite Raimonda , Duzinaite Simona , Krasauskas Virgilijus , Valickas Raimondas , Zilaitiene Birute

Introduction: Parathyroid carcinoma (PC) is an extremely rare, aggressive and life-threatening form of primary hyperparathyroidism (pHPT). PC accounts for less than 1% of cases of pHPT, predominantly diagnosed in the fifth or sixth decades of life. Most parathyroid carcinomas are diagnosed after surgery.Case description: A 51-year old man was admitted to the Hospital of Lithuanian University of Health Sciences, Kaunas clinics due to leg pain and general ...

ea0081ep608 | Endocrine-Related Cancer | ECE2022

Clinical case: MEN1 syndrome

Meskinyte Ieva , Cyrolyte Saule , Strazdiene Igne , Urbonaviciute Egle , Klimaite Raimonda , Jakubonienė Neli

Introduction: Multiple Endocrine Neoplasia Type 1 (MEN1) is a rare, autosomal dominantly inherited syndrome that causes tumors of the endocrine glands [1]. This syndrome is most commonly associated with neuroendocrine tumors of the parathyroid glands, pituitary gland and pancreas [2].Case: A 30-year-old woman was admitted to the Hospital of Lithuanian University of Health Sciences, Kaunas Clinics for unconsciousness and significant hypoglycaemia: 1.0 - 3...