Searchable abstracts of presentations at key conferences in endocrinology

ea0081p522 | Adrenal and Cardiovascular Endocrinology | ECE2022

Gastric monomorphic epitheliotropic intestinal T-cell lymphoma with bilateral adrenal metastases

Kaliakatsou Eirini , Markou Athina , Papanastasiou Labrini , Giagourta Irini , Kalantzi Athanasia , Dimitriadi Anastasia , Lenos Michael , Kounadi Theodora , Fountas Athanasios

Introduction: Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL), formerly known as type II enteropathy-associated T-cell lymphoma, is a rare and aggressive subtype of lymphoma of the gastrointestinal track typically noted in Asian or Hispanic populations. Adrenal involvement as part of MEITL is extremely rare. Herein we present a patient of Greek origin with MEITL and bilateral adrenal metastases.Case Presentation: A 74-year-old man presente...

ea0081p8 | Adrenal and Cardiovascular Endocrinology | ECE2022

Pre-, peri- and post-operative characteristics of biochemically silent pheochromocytomas: a case series

Fountas Athanasios , Kanti Georgia , Glikofridi Spyridoula , Kalantzi Athanasia , Giagourta Irini , Markou Athina , Christou Maria , Tigas Stelios , Ntali Georgia , Aggeli Chrysanthi , Zografos Giorgos , Saoulidou Eleftheria , Dimakopoulou Antonia , Kounadi Theodora , Papanastasiou Labrini

Introduction: Pheochromocytomas (PCs) and paragangliomas are rare tumours occurring in about 0.6 cases per 100,000 person-years. Biochemically silent PCs with normal catecholamine levels due to lack of catecholamine secretion or subtle secretion within the established normal levels are even rarer. Up to date, biochemically silent PCs are poorly investigated.Aim: To assess the pre-, peri- and post-operative characteristics of patients with biochemically s...

ea0063ep18 | Adrenal and Neuroendocrine Tumours | ECE2019

Characteristics, management and outcome of patients with adrenocortical carcinoma in a tertiary hospital: a retrospective study

Papanastasiou Labrini , Choreftaki Theodosia , Zografos George , Kapsali Chara , Kalantzi Athanasia , Monastirioti Nikoleta , Gravvanis Christos , Glykofridi Spyridoula , Tyfoxilou Ernestini , Vlaxou Sofia , Charalampidou Liana , Voulgaris Nikos , Markou Athina , Giagourta Irini , Piaditis George , Kounadi Theodora

Adrenocortical carcinoma (ACC) is a rare, aggressive tumor with poor prognosis, affecting 0.5–2 cases/106population/year.Objective: To analyse retrospectively characteristics, management and outcome of ACC patients, followed in our center between 2010–2018.Material and methods: The medical records related to diagnosis, treatment and follow-up of nine patients of 59.2±13.8 years with histological diagnosis ...