Searchable abstracts of presentations at key conferences in endocrinology

ea0006ds10 | Management of the hypertensive diabetic patient | SFE2003

Diabetic Hypertension: Best Left to the Cardiologist

de Belder A

The author will discuss the practicalities and philosophy of diabetic patients being looked after by the wrong doctor.An evidence-based approach will be dismissed in favour of politically driven targets and the talk might be presented by a Department of Health clone (results awaited).A prejudicial review of medical history will be used to emphasise the superiority of the cardiologist over the management of the diabetic patient with...

ea0029p475 | Clinical case reports - Thyroid/Others | ICEECE2012

Persistently abnormal thyroid function in a 26 year old Afro-Caribbean man: a diagnostically challenging case

De Souza L. , Ormerod J. , De P.

Introduction: While most common aetiologies accounting for hyperthyroidism are straightforward and respond predictably to treatment, a subset provides diagnostic or therapeutic challenge. We report such a case.Case report: A 26-year-old Afro-Caribbean male presented with symptoms of thyrotoxicosis. FT4 was 50 (12–20 pmol/l), FT3 11.5 (3–8 pmol/l) and TSH 5.38 (0.27–4.20 mU/l). He had diffuse non-tender thyromegaly without eye signs. Thyroi...

ea0011p110 | Clinical case reports | ECE2006

Post-partum thyroiditis (PPT): colour-doppler ultrasonography evaluation

De Remigis P , De Remigis A , Vianale L

Colour-Doppler Ultrasonography (CDU) is applied to the study of many thyroid diseases. In the last one semiquantitative (colour-signal) and quantitative (peak flow velocity at inferior thyroid artery) evaluations are considered. Graves’ disease (GD), amiodarone-induced thyrotoxicosis were better characterized, even Hashimoto thyroiditis and De Quervain thyroiditis were studied. We described a case of Silent Thyroiditis (ST), showing the possibility to distinguish it from ...

ea0057036 | ACTH independent hypercorticism with normal adrenal imaging and negative genetic screening for micronodular adrenal disease in a female teenager: what to suspect? | BES2018

ACTH independent hypercorticism with normal adrenal imaging and negative genetic screening for micronodular adrenal disease in a female teenager: what to suspect?

Van De Maele K , De Schepper J

Introduction: Micronodular adrenocortical disease is a very rare cause of Cushing syndrome in children. This adrenocorticotropic hormone (ACTH)-independent form of Cushing syndrome is mostly a part of the Carney Complex, which is caused by mutations in the PRKAR1A gene (1). A young female with endogenous ACTH independent hypercorticism without the classical gene mutations in the pigmented and the non-pigmented form of micronodular adrenal disease is presented.<p c...

ea0051dp3.3 | Diabetes professional day: Session 3 | BSPED2017

Obesity, diabetes and metabolic syndrome

de Alwis Nimantha

The prevalence of Obesity is increasing worldwide. This is due to a deterioration in dietary habits and lack of physical exercise in a genetically predisposed population. Obesity can commence in childhood and be progressive. Early detection, population wide education regarding prevention and early intervention is extremely important. The management of obesity must include an individualized evaluation and suitable, achievable plan. Obesity can be progressive through adolescence...

ea0081d1.1 | PRRT or targeted molecular therapies as preferred line of treatment | ECE2022

For: PRRT or targeted molecular therapies as preferred line of treatment

de Herder Wouter W

Purpose: Bronchopulmonary (BP) and gastroenteropancreatic (GEP) neuroendocrine neoplasms (NEN) are slow-growing tumors, which frequently express somatostatin receptors on their cell membranes. These receptors are targets for therapy with 177Lutetium-labeled somatostatin analogues.Experimental Design: Patients receive four treatments of 177Lu-DOTATATE at a dose of 7.4 GBq every 8 weeksResults: An objective resp...

ea0063mte1 | (1) | ECE2019

The road from flash glucose monitoring to hybrid closed loop systems: keys to success.

De Block Christophe

Living with type 1 diabetes (T1D) is challenging and requires intensive glucose monitoring and titration of insulin in order to obtain near-normal glucose levels to reduce the risk of complications. However, changes in dietary intake and level of activity can cause large glucose excursions. Continuous glucose monitoring systems, either intermittently scanned either real-time, can provide a comprehensive picture of glucose profiles, allowing patients to make therapeutic adjustm...

ea0063mte14 | (1) | ECE2019

How multidisciplinay care and tailor-made transition save lives of young adults with Prader-Willi syndrome

de Graaff Laura

Introduction: Due to improved pediatric care, life expectancy of children with complex genetic syndromes (CGS) is increasing. Many children with CGS now do reach adult age and have to make the transition to adult endocrine healthcare. However, many adult endocrinologists are not yet prepared for the increasing number of adults with CGS. Although patients receive multidisciplinary (MD) care at the pediatric department, MD care is not yet available for most adults with CGS. Also...