Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep676 | Pituitary and Neuroendocrinology | ECE2022

Idiopathic isolated adrenocorticotropic hormone deficiency

Komzia Paraskevi , Gogakos Apostolos , Kalograni Fanny , Tsoutsas Georgios , Kita Marina , Efstathiadou Zoi

Introduction: Idiopathic Isolated Adrenocorticotropic hormone (ACTH) deficiency (IIAD) is a rare cause of secondary adrenal insufficiency. It can present with a variety of clinical symptoms, mainly chronic fatigue and euvolemic hyponatraemia, and may coexist with autoimmune disease, most commonly Hashimoto’s thyroiditis. Radiographically, an empty sella turcica image can be seen. We present 3 cases of isolated ACTH deficiency.Case 1: A 47-year-old w...

ea0063p889 | Diabetes, Obesity and Metabolism 3 | ECE2019

Radiation-induced loss of glycemic control in a patient with refractory lymphoma

Adamidou Fotini , Komzia Paraskevi , Georgiou Thomas , Tsoutsas Georgios , Panagiotou Athanasios , Kita Marina

Introduction: PD-1 inhibitors are powerful disruptors of self- tolerance and autoimmune diabetes develops in up to 0.9% of patients. Lipodystrophic insulin reactions, although uncommon with human insulin analogs, are a recognized cause of impaired insulin delivery in patients on intensive insulin regimens. We describe a patient with resistant lymphoma and nivolumab-induced autoimmune diabetes, who suffered loss of glycemic control due to early radiation-induced subcutaneous fi...

ea0056p689 | Adrenal cortex (to include Cushing's) | ECE2018

Absent adrenarche in adults with congenital hypopituitarism

Adamidou Fotini , Christoforidis Athanasios , Tsoutsas Georgios , Tsatsou Frangiski , Lazarou Lazaros , Kita Marina

Background: The mechanisms regulating adrenarche have not been elucidated, although evidence supports a critical role for ACTH and possibly other unidentified pituitary or adrenal contributing factors. Absent adrenarche has been described in children with a variety of sellar tumors. We describe a case series of five adults with congenital hypopituitarism and absent adrenarche.Cases: Three females and two males with “idiopathic” congenital hypop...

ea0037ep699 | Pituitary: basic and neuroendocrinology | ECE2015

Addisonian crisis as a manifestation of a partially empty sella in a 68-year-old woman

Mouslech Zadalla , Somali Maria , Sakali Anastasia-Konstantina , Koulara Pavlina , Mourouglakis Alexandros , Tsoutsas Georgios , Savopoulos Christos , Mastorakos George , Hatzitolios Apostolos Ioannis

Introduction: Empty sella syndrome (EES) is a condition often discovered incidentally, where the sella turcica, the structure containing the pituitary gland, appears to be empty. Patients either remain asymptomatic or, rarely, manifest signs of declined pituitary function. Patients experiencing hypopituitarism are offered hormonal replacement. Autopsy studies estimated a 5% EES prevalence among healthy individuals.Case report: A 68-year-old post-menopaus...

ea0037ep700 | Pituitary: basic and neuroendocrinology | ECE2015

Fracture of the left wrist as a possible indication of Cushing's disease

Mouslech Zadalla , Somali Maria , Sakali Anastasia-Konstantina , Kakaletsis Nikolaos , Tsoutsas Georgios , Savopoulos Christos , Mastorakos George , Hatzitolios Apostolos Ioannis

Introduction: Cushing’s syndrome is a rare (0.004%) hormonal disorder, which develops due to hypercortisolaemia. Cushing’s disease refers to a corticothroph cell pituitary tumour overproducing ACTH, which induces abnormally increased cortisol production from the adrenal glands. Cushing’s disease is a causative factor of osteoporosis, hypertension, glucose intolerance and dyslipidaemia.Case report: A 50-year old woman was referred to our de...