Searchable abstracts of presentations at key conferences in endocrinology

ea0056p709 | Clinical case reports - Pituitary/Adrenal | ECE2018

Successful management of Cushing’s disease in pregnancy: a case report

Batman Adnan , Ozturk Feyza Yener , Sen Esra Cil , Erol Rumeysa Selvinaz , Canat Muhammed Masum , Saygili Emre Sedar , Cakir Sezin Dogan , Basmaz Seda Eren , Yildiz Duygu , Altuntas Yuksel

Introduction: Cushing’s disease (CD) frequently leads to hypogonadotropic hypogonadism by hypercortisolism and hyperandrogenemia. In the literature, there are totally 96 cases of CD and pregnancy. Only four of 11 cases, operated transsphenoidally, were cured. We aimed to present a case of CD developing pregnancy in which hypercortisolism was successfully controlled by transsphenoidal surgery (TSS) in 2nd trimester.Case report: 28 years old female wa...

ea0056ep84 | Diabetes, Obesity and Metabolism | ECE2018

A case report of MODY 2 treated as type 2 diabetes mellitus in pregnancy

Batman Adnan , Saygili Emre Sedar , Basmaz Seda Eren , Cakir Sezin Dogan , Yildiz Duygu , Ozturk Feyza Yener , Sen Esra Cil , Erol Rumeysa Selvinaz , Canat Muhammed Masum , Altuntas Yuksel

Introduction: Maturity-onset diabetes of young (MODY) type 2 is caused by mutation of the glucokinase gene. It is characterized by mild fasting hyperglicemia and absence of vascular complications. It is estimated that the incidence of gestational diabetes is 3%. We aimed to present a pregestational diabetic case with MODY-type 2 in pregnancy.Case report: A 38-year-old pregnant woman was referred to our clinic for glycemic regulation at 22th week of gesta...

ea0056ep95 | Interdisciplinary endocrinology | ECE2018

A case with autoimmune polyglanduler syndrome type 3A

Batman Adnan , Erol Rumeysa Selvinaz , Ozturk Feyza Yener , Sen Esra Cil , Canat Muhammed Masum , Saygili Emre Sedar , Cakir Sezin Dogan , Basmaz Seda Eren , Yildiz Duygu , Altuntas Yuksel

Introduction: Autoimmune polyendocrine syndromes (APS) are rare endocrinopathies characterized by the coexistence of at least two glandular autoimmune diseases. APS comprise a wide spectrum of autoimmune disorders and are divided into a very rare juvenile (APS type 1) and a more common adult type with (APS 2) or without adrenal failure (APS 3). We present a patient with polyglanduler syndrome type 3a.Case report: A 39-years-old female patient was present...