Searchable abstracts of presentations at key conferences in endocrinology

ea0056p287 | Bone & Osteoporosis | ECE2018

Case report: male adult with autosomal-dominant osteopetrosis

Schmidt Sebastian , Lehmann Gabriele , Alfons Muller Ullrich , Wolf Gunter

Background: Osteopetrosis is a rare chronic bone disease with high bone mineral densitiy due to impaired osteoclast activity or development. Genetic mutations result in severe infantile (autosomal recessive, incidence 1:200,000) and less severe adult forms (autosomal-dominant osteopetrosis/ADO). The incidence is estimated at 1:20,000 for noninfantile forms. In adults osteopetrosis is often asymptomatic with increased risk for bone fracture. Treatment is symptom-based (e.g. cal...

ea0041ep866 | Pituitary - Basic | ECE2016

Retrospective evaluation of pituitary tumours in a single tertiary care institution

Askitis Dimitrios , Kloos Christof , Battefeld Wilgard , Wolf Gunter , Muller Ulrich Alfons

Introduction: We retrospectively evaluated all patients with pituitary tumours treated in our department from 1.1.1997–1.11.2014Patients and methods: 215 patients (124 females: 91 males, mean age 50,9 y.) were treated because of pituitary tumours. All patients underwent basal hormonal analysis and testing in order to check for hormonal activity. Pituitary masses were divided into groups concerning their hormonal status and were further classified ac...

ea0035p528 | Endocrine tumours and neoplasia | ECE2014

Retrospective evaluation of adrenal incidentalomas in a tertiary care institution

Askitis Dimitrios , Kloos Christof , Battefeld Wilgard , Wolf Gunter , Dirsch Olaf , Mueller Ulrich Alfons

Introduction: We retrospectively evaluated all patients with adrenal tumours treated in our Department from 1.1.1999 to 1.10.2013.Patients and methods: 189 patients (110 females: 79 males, mean age of 57.5 years) were treated because of adrenal tumours. All patients underwent hormonal analysis and testing in order to check for hormonal activity. Tumours were classified according to gender, age at diagnosis, tumour localisation and size, as well as benign...

ea0070ep7 | Adrenal and Cardiovascular Endocrinology | ECE2020

Case report: Ectopic Cushing syndrome as paraneoplastic manifestation of an advanced small cell lung cancer

Schmidt Sebastian , Werner Christoph , Kloos Christof , Yomade Olaposi , Gabriela Schrenk Karin , Hochhaus Andreas , Wolf Gunter

Background: Ectopic Cushing Syndrom (ECS) represents approximately 12% of all patients with Cushing´s disease. Either ACTH (5–10%), CRH or cortisol is produced uncontrolled from nonpituitary tissue. Half of ECS cases are neuroendocrine lung tumors [carcinoid tumors > small cell lung carcinoma (SCLC)], but ECS is clinically apparent only in 1–5% of SCLC cases. Clinical features vary according to extent and duration of exposure to ACTH/Cortisol excess and in...

ea0041gp94 | Diabetes (2) | ECE2016

Calculated creatinine clearance using the CKD-EPI-formula shows a reliable prediction and high correlation to 24-h-urine in patients with diabetes mellitus but underrates systematically potentially leading to withdrawal or no prescription of oral antidiabetics

Kloos Christof , Muller Nicolle , Anschutz Julia , Klein Friederike , Burghardt Katharina , Schmidt Sebastian , Schmidt Irina , Boer Klas , Wolf Gunter , Muller Ulrich

Introduction: To reliably assess glomerular filtration is of vital importance if oral antidiabetics are used. We compared the CKD-EPI model, a clinically established calculation model to assess creatinine clearance (CreaClear) with specimens from 24-h urine.Method: Inpatients (university hospital) with diabetes mellitus received a 24-h urine collection (24hClear) or since 2013 calculated CreaClear using CKD-EPI-formula (EPI). From 2014 to 2015 values of ...