Searchable abstracts of presentations at key conferences in endocrinology

ea0032p1033 | Thyroid (non-cancer) | ECE2013

Internal jugular vein thrombosis and intensely hypermetabolic thyroid on 18F-FDG PET/CT

Boscolo Marina , Corvilain Bernard

Internal jugular vein thrombosis (IJVT) is generally related to central venous access devices (CVADs) because of endothelial trauma or inflammation. Other reported causes include neck surgery complication, malignancies, deep neck infections, intravenous drug abuse, ovarian hyperstimulation syndrome and hypercoagulable states.We report the case of a 47-year-old woman presenting with acute neck pain, local swelling and fever. Neck ultrasound with Doppler s...

ea0032p217 | Clinical case reports – Pituitary/Adrenal | ECE2013

Histologically surprising nasal polyps

Boscolo Marina , Devuyst France , Corvilain Bernard

Pituitary macroadenomas usually present with symptoms due to a local mass effect or to hormone abnormalities. Acromegaly is due an excessive GH production, usually caused by a slow-growing pituitary adenoma. Acromegaly is an insidious disease. An average delay of 7 years is reported between the time of symptoms onset and diagnosis. According to main symptoms, acromegaly is usually diagnosed by internists, ophthalmologists or rheumatologists. It may be suspected by pneumologist...

ea0056gp217 | Reproduction | ECE2018

The first Belgian series of 56 patients with congenital hypogonadotropic hypogonadism (CHH): genetic and brain abnormalities

Valdes-Socin Hernan , Libioulle Cecile , Harvengt Julie , Pintiaux Axelle , Jonas Christelle , Parent Anne Simone , Geenen Vincent , Corman Vincianne , Debray Francois Guillaume , Dideberg Vincianne , T'Sjoen Guy , De Leerner Anne , Beckers Dominique , Destree Anne , Roland Dominique , Lederer Damien , Boscolo Marina , Bours Vincent , Maiter Dominique , Beckers Albert

Introduction: CHH is a genetic syndrome that combines reproductive and brain abnormalities. The brain phenotype has been incompletely characterized. We aimed to study neuroradiological and genetic features in this first Belgian series of patients with CHH.Methods: A series of 56 adult patients (48 males, 8 females) presenting with CHH was investigated for a panel of 16 genes related to hypogonadotropic hypogonadism by next generation sequencing on a MiSe...