Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep856 | Pituitary and Neuroendocrinology | ECE2023

Carcinoid Syndrome With Mesenteric Ischemia

Alkan Ozlem , Koksalan Damla , Selek Alev , Canturk Zeynep , Cetinarslan Berrin

Introduction: Carcinoid tumors are included in the neuroendocrine tumor family. They are usually seen in the gastrointestinal tract and are asymptomatic unless liver metastases are present.Case Report: A 44-year-old male patient was admitted with chronic crampy abdominal pain, diarrhea, and redness of the face and neck. He was admitted to the emergency department for abdominal pain many times before and was hospitalized in the general surgery department ...

ea0090p669 | Endocrine-related Cancer | ECE2023

Clinical findings, treatment modality and outcomes of adrenocortical carcinoma: a retrospective review of single tertiary center experience

Selek Alev , Koksalan Damla , Sozen Mehmet , Gezer Emre , Alkan Ozlem , Canturk Zeynep , Cetinarslan Berrin

Background & Aim: Adrenocortical carcinoma (ACC) is an extremely rare malignancy usually with poor outcomes, although the prognosis varies greatly depending on the initial tumor stage. Here we present clinical and outcome diversity of the patients in a single center.Methods: We retrospectively analyzed 16 patients with ACC diagnosed between 2000 and 2022. Demographical findings, hormonal status, radiological findings, ENSAT stage, weiss score and Ki6...

ea0099ep1255 | Late Breaking | ECE2024

A case of langerhans cell histiocytosis accompanying hypothalamus, mastoid bone and liver involvement

Acar Saadet , Cetinarslan Berrin , Canturk Zeynep , Selek Alev , Gezer Emre , Koksalan Damla , Alkan Ozlem , Oktem Fatma

Introduction: Langerhans cell histiocytosis (LCH) is a multisystem neoplastic disease with primarily bone and skin involvement. Although its pathogenesis is still not fully understood, LCH lesions contain clonal CD 207+ dendritic cells with the frequently identified BRAF V600E mutation and an inflammatory component. Although isolated central nervous system involvement is extremely rare, a common site of involvement is the hypothalamic-pituitary axis.Case...

ea0090ep1031 | Thyroid | ECE2023

Combination of recurrent thyroid artery embolization and sorafenib treatment in the management of inoperable papillary thyroid cancer

Koksalan Damla , Cam İsa , Cetinarslan Berrin , Canturk Zeynep , Selek Alev , Gezer Emre , Sozen Mehmet , Alkan Ozlem

Introduction: Thyroid papillary cancer is a solid organ malignancy that can be cured mostly by surgical and radioactive iodine(RAI) therapy. Metastatic disease state and radioactive iodine resistance have led to new treatment searches. In recent years, sorafenib, a tyrosine kinase inhibitor, has been used as a first-line treatment in thyroid papillary cancers that cannot be cured by surgery or radioactive iodine treatment. In addition, the use of thermal ablation and transarte...

ea0099ep1304 | Late Breaking | ECE2024

Efficacy and side effects of subcutaneous pasireotide alone or in combination with cabergoline in patients with cushing’s disease whithout postoperative remission

Selek Alev , Demir Nurgul , Cetinarslan Berrin , Canturk Zeynep , Gezer Emre , Sozen Mehmet , Koksalan Damla , Alkan Ozlem , Acar Saadet , Oktem Fatma

Pasireotide is a second-generation, multireceptor-targeted somatostatin receptor ligand and is approved for the treatment of patients with Cushing’s Didease (CD) for whom surgery has failed or is not an option. This retrospective single center study aims to report the efficacy, side effects and follow-up of the treatment with pasireotide alone or in combination with cabergoline in patients without remission after transsphenoidal surgery. Among 187 patients with CD, 15 pat...