Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep805 | Pituitary: clinical | ECE2015

Pituitary apoplexy in GH-deficient adults treated with GH – a KIMS database retrospective study

Radian Serban , Jonsson Peter J , Camacho-Hubner Cecilia , Biller Beverly M K , Buchfelder Michael , AEkerblad Ann-Charlotte , Korbonits Marta

Background: Pituitary apoplexy (PitApo) has significant associated-morbidity and its management is not yet standardised.Aim: To describe prevalence and characteristics of PitApo patients in GH deficient (GHD) patients compared with two control populations.Patients and methods: Patients with ‘infarction-apoplexy’ GHD aetiology code were identified from Pfizer International Metabolic Database (KIMS). Baseline characteristic...

ea0022p629 | Neuroendocrinology and Pituitary (<emphasis role="italic">Generously supported by Novartis</emphasis>) | ECE2010

Flexion contractures syndrome as the initial manifestation of hypopiptuitarism

Insaf Hadj Ali , Karima Khiari , Nadia Mchirgui , Youssef Lakhoua , Nejib Ben Abdallah

We present a 58 years old woman admitted in our department for bradycardia, diarrhea, epigastralgia, anorexia and weight loss. Physical examination showed low blood pressure and inability to walk or stand due to severe flexion contractures of the lower extremities without neurological abnormalities. The biological findings showed severe hyponatremia, hyerkaliemia tendency, low levels of plasma cortisol and ACTH suggesting pituitary adrenal axis deficiency. Hormonal investigati...

ea0037ep801 | Pituitary: clinical | ECE2015

Analysis of the aetiology of hypopituitarism: the results from double centre study

Caliskan Mustafa , Basaran Mehtap Navdar , Beysel Selvihan , Arslan Muyesser Sayki , Ucan Bekir , Tuna Mazhar Muslum , Cakal Erman , Berker Dilek Sensoz , Guler Serdar , Delibasi Tuncay

Introduction: Hypopituitarism is commonly acquired in adult life and its main causes are pituitary tumors and/or their treatments, empty sella syndrome and etc.Patients and methods: A double centre, cross-sectional database study was performed in Turkish population for last 10 years to investigate the etiology of hypopituitarism. One-hundred forty nine patients were included (53% female and 47% male) with a mean age of 47.9±15.6 years (ranging from ...

ea0032p234 | Clinical case reports – Pituitary/Adrenal | ECE2013

Combined choroidal neovascularization and hypopituitarism in a patient with homozygous mutation in methylenetetrahydrofolate reductase gene

Aydogdu Aydogan , Haymana Cem , Baskoy Kamil , Durukan Ali Hakan , Ozgur Gokhan , Azal Omer

Introduction: Hypopituitarism is defined as either partial or complete deficiency of anterior or posterior pituitary hormone secretion or both. Hypopituitarism itself may increase the risk of thromboembolism/hypercoagulopathy, and underlying mechanisms of hemostatic dysfunctions in hypopituitarism are mostly unknown. Reduced enzymatic activity due to methylenetetrahydrofolate reductase (MTHFR) gene mutations are associated with hyperhomocysteinemia and have been linked to both...

ea0026p170 | Neuroendocrinology | ECE2011

Metabolic encephalopathy and quadriparesis induced by severe hyponatremia in the patient with Sy Seehan

Bogdanovic Jelena , Perusko Radmila Stojanovic , Popovic Dragana , Dzomlija Radojka , popovic Vera , Ercegovac Marko , Bogdanovic Ljiljana , Micic Dusan

Sy Sheehan or postpartal pituitary necrosis presents with symptoms and signs of hypopituitarisms. It is usually a consequence of complicate delivery followed by intensive uterine bleeding. Diagnosis can be delayed years after delivery, up to 20 years.We present a case of 51-year-old female patient. She was admitted in the department of neurology in the Emergency center, Belgrade, with disturbance of consciousness. Few days before she felt leg weakness an...

ea0081ep818 | Pituitary and Neuroendocrinology | ECE2022

Hypopituitarism in tropical countries

Ega Lakshman kumar , sahay rakesh , kudugunti neelaveni

Background: Etiology of hypopituitarism differs in tropical countries compared to the West and includes pituitary abscess, snake bite, HIV infection, Sheehan syndrome, road traffic accidents, iron overload states etc.Aims and Objectives: The present case series highlights the spectrum of hypopituitarism in tropical countries.Case Details: 1. C1: 23 y/o female presented with loss of consciousness, unrecordable BP and hypoglycemia. H...

ea0022p323 | Diabetes | ECE2010

Etiologies of patients admitted to emergency department with hypoglycemia

Eren Hakan , Caliskan Haci Mehmet , Kilicli Fatih , Korkmaz Ilhan , Acibucu Fettah , Dokmetas Sebila

Introduction: Hypoglycemia is the most common endocrinological problem in emergency departments.Objective: To explore the causes of hypoglycemia in patients who were admitted to the emergency department with symptoms resembling hypoglycemia.Design: In our study, 225 hypoglycemia cases were evaluated from January 2000 to May 2008.Results: Of 225 hypoglycemia cases, 158 (70.2%) receiving treatment for diabetes ...

ea0020p269 | Clinical case reports and clinical reports | ECE2009

Lymphocytic hypophysitis case who developed empty sella to follow up

Dokmetas Sebila , Kilicli Fatih , Timucin Meryem , Acibucu Fettah

Lymphocytic hypophysitis (LH), an uncommon pituitary disorder that is considered an autoimmune disease. The disease shows a striking female predilection of ~9:1 and commonly affects young women during late pregnancy or in the postpartum period. Less frequently, it has also been observed in men and postmenaposal woman. Partial or total hypopituitarism can be in LH. In the early stage, the pituitary gland is enlarged like a pituitary tumor, from which it cannot be distinguished ...

ea0003p45 | Clinical Case Reports | BES2002

Growth hormone deficiency in salt-losing congenital adrenal hyperplasia

Traggiai C , Conway G , Stanhope R

Introduction: Congenital adrenal hyperplasia (CAH) is characterised by impaired gluco and mineralocorticoid and excessive adrenal androgen secretion from the adrenal cortex. More than 90% of cases of CAH are caused by defects in the steroid 21-hydroxylase (CYP21) gene. We describe the association between salt-losing 21-hydroxylase deficiency and growth hormone deficiency.Patients and Methods: We reviewed 4 patients with salt-losing CAH (CYP21), who pres...

ea0056p833 | Pituitary - Clinical | ECE2018

Registry for central diabetes insipidus in Russia: prevalence and etiologies of the disease

Pigarova Ekaterina , Dzeranova Larisa , Belaya Zhanna , Rozhinskaya Liudmila , Lutsenko Alexander , Melnichenko Galina , Dedov Ivan , Consortium CDI The

Introduction: Epidemiological data for central diabetes insipidus (CDI) are quite sparse.Objectives: To provide an epidemiological data on CDI in different regions of Russia (20 from 83 Federal regions).Materials and methods: We used the Russian Registry for Central Diabetes Insipidus (RCDI) to study the epidemiological features of CDI.Results: A total of 2004 patients with CDI were recorded, 47% women and 59...