Searchable abstracts of presentations at key conferences in endocrinology

ea0073aep856 | Late Breaking | ECE2021

A rare case of glucagonoma presented with high serum amilase and lipase

Topaloglu Oya , Tayfur Yurekli Oyku , Metindogan Onur , Arda Inan Mehmet , Ali Sendur Mehmet , Ersoy Osman , Ersoy Reyhan , Cakir Bekir

IntroductionGlucagonoma is an extremely rare type of functional pancreatic neuroendocrine tumor that is characterized by distinctive clinical manifestations such as diabetes mellitus, weight loss, deep vein thrombosis, and necrolytic migratory erythema which represents the hallmark clinical sign of glucagonoma syndrome. Here, we report the case of a 53-year-old male patient who presented with high amilase and lipase levels. In further investigation a pan...

ea0073aep872 | Late Breaking | ECE2021

A rare cause of malignant pleural effusion: Poorly differentiated thyroid carcinoma

Helvaci Burcak , Karaahmetli Gulsum , Sacikara Muhammet , Cuhaci Seyrek Neslihan , İrem Serifoglu , Aydin Cevdet , Topaloglu Oya , Ersoy Reyhan , Cakir Bekir

PurposePoorly differentiated thyroid carcinoma (PDTC); is a rare type of thyroid cancer with a high risk of recurrence, metastasis, and death. Pleural effusion due to thyroid cancer has seldom been reported. In this report, we present a case with PDTC related malignant pleural effusion.CaseA 66-year-old male patient presented with neck swelling and shortness of breath. At another center, thyroid ultrasonograp...

ea0073aep882 | Late Breaking | ECE2021

Clinical and pathological features of thyroid cancer in adolescents and young adults

Bestepe Nagihan , Dirikoc Ahmet , Baser Husniye , Yazicioglu Omer , Aksoy Altinboga Aysegul , Topaloglu Oya , Ersoy Reyhan , Cakir Bekir

IntroductionThyroid cancer is the most common endocrine malignancy and its overall incidence has increased significantly in the last 30 years. Cancer in adolescents and young adults (AYA) is defined by the National Cancer Institute as diagnoses occurring among those aged 15 to 39 years. Thyroid cancer is the second most common cancer in the AYA population. In this study, we aimed to compare clinical, ultrasonographical, cytological and histopathological ...

ea0073aep884 | Late Breaking | ECE2021

A tru-cut biopsy proven rare thyroid neoplasia in a giant nodule with a benign fine needle aspiration cytology

Leyla Akdoğan , Ahmadova Konul , Bestepe Nagihan , Burcak Polat Sefika , Dilek Imdat , Aydin Cevdet , Topaloglu Oya , Ersoy Reyhan , Cakir Bekir

IntroductionExtramedullary plasmacytoma (EMP) is a plasma cell neoplasm of extraosseous tissues. Less than 5% of all plasma cell neoplasms develop extramedullary. EMP is most common in the upper respiratory tract and oral cavity. The thyroid gland is one of the extremely rare regions. It is more common in men and the average age at diagnosis is 55. Primary thyroid plasmacytoma is one of the rare thyroid neoplasms. It often manifests as a rapidly growing ...

ea0073ep239 | Late Breaking | ECE2021

A rare cause of levothyroxine malabsorption: İleostomy

Leyla Akdoğan , Ahmadova Konul , Sacikara Muhammed , Ali Tam Abbas , Ozdemir Didem , Topaloglu Oya , Ersoy Reyhan , Cakir Bekir

IntroductionIt is recommended to determine levothyroxine (LT4) dose individually in patients with hypothyroidism. However, higher doses of LT4 therapy are required to achieve target TSH levels in significant number of patients. Oral LT4 absorption occurs in the small intestine, especially in the jejunum and proximal ileum, while a small amount is absorbed in duodenum. Causes of LT4 malabsorption include helicobacter pylori infection, chronic atrophic gas...

ea0099ep1092 | Adrenal and Cardiovascular Endocrinology | ECE2024

A rare association of salt-wasting congenital adrenal hyperplasia and type 1 diabetes mellitus

Soyer Ahmet , Aksu Hatice , Ayrancİ Esma , Dibeklioglu Bilge , Polat Sefika , Topaloglu Oya , Ersoy Reyhan , Cakir Bekir

The co-occurrence of congenital adrenal hyperplasia and type 1 diabetes mellitus (T1DM) is a rare phenomenon in existing literature. The primary cause of congenital adrenal hyperplasia (CAH) is often 21-hydroxylase deficiency (21OHD), a condition associated with the CYP21A2 gene located on chromosome 6p21.3 within the major human leukocyte antigen (HLA) histocompatibility locus. Various gene polymorphisms, particularly in HLA-DQalpha, DQbeta, and DR genes on chromosome 6p21.32...

ea0099ep960 | Thyroid | ECE2024

Atypical subacute thyroiditis associated with papillary thyroid carcinoma in a case of Graves’ disease

Keskin Muge , Solmaz Kubra , Aydın Cevdet , Taneri Ferit , Bilezikci Banu , Topaloglu Oya , Ersoy Reyhan , Cakır Bekir

Aim: In patients with papillary thyroid carcinoma (PTC), the incidence of subacute thyroiditis (SAT) is thought to be more frequent than estimated. The incidence of thyroid cancer is between 2.3% and 21.1% in Graves’ Disease (GD).Case: A 31-year-old female patient applied with complaints of amenorrhea and hair loss in the 10th postpartum month. There was no history of COVID-19 infection, but Biontech vaccine were administered two years ago. Her fami...

ea0081p514 | Late-Breaking | ECE2022

Superior vena cava syndrome associated with graves’ disease

Durmaz Himmet , Arifoglu Unzile , Omer Yazıcıoglu Mustafa , Sacıkara Muhammed , Nasıroglu İmga Narin , Topaloglu Oya , Ersoy Reyhan , Cakir Bekir

Introduction: Goiter means that the thyroid gland is larger than the normal size for the patient’s age and gender. Some of the causes of goiter are iodine deficiency, thyroid nodules, Graves’ disease(GD). Goiter, hyperthyroidism, ophthalmopathy and dermopathy can be seen in GD. Compression symptoms due to goiter (dyspnea, dysphagia, superior vena cava syndrome) are also seen. Here, we will present a case of GD with superior vena cava syndrome.C...

ea0081p515 | Late-Breaking | ECE2022

Parathormone washout in cytology of Suspicious for Follicular Neoplasm

Durmaz Himmet , Cavnar Helvacı Burcak , Beştepe Nagihan , Aksoy Altınboğa Ayşegul , Dirikoc Ahmet , Topaloglu Oya , Ersoy Reyhan , Cakir Bekir

Introduction: The risk of malignancy in thyroid nodules is reported by the Bethesda system by performing fine needle aspiration biopsy (FNAB). Atypia of undetermined significance(AUS) or follicular lesion of undetermined significance(FLUS)(Bethesda 3) and suspicious for a follicular neoplasm (Bethesda 4) create uncertainty about treatment and follow-up. Molecular tests, ultrasonographic features of the nodules, and calcitonin level help us for this uncertainty. Here, we will p...

ea0090p772 | Thyroid | ECE2023

Predictive factors for sufficient cytological result after first nondiagnostic thyroid fine-needle aspiration biopsy result

Dilek Dellal Kahramanca Fatma , Bestepe Nagihan , Meryem Kiran Merve , başer husniye , Ozdemir Didem , Topaloglu Oya , Ersoy Reyhan , Cakir Bekir

Aim: To determine whether there is any factor that can predict sufficient results in second thyroid fine-needle aspiration biopsy (FNAB) after first nondiagnostic cytological result.Materials and method: Nodules with non-diagnostic result after first FNAB were included and separated into two groups as sufficient (Group-1) and insufficient (Group-2) second FNAB. Results: Second FNAB was performed on 643 nodules of 443 patients with ...