Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep1017 | Thyroid | ECE2023

Achalasia associated with Grave’s disease: case report

Bensmaine Faiza , Beloucif Lynda , Guglielmi Jean-Marc , Botella Camille , Quittelier Regis , Pierre Jean Guillausseau

Rationale: Grave’s disease (GD) is the most common subtype of autoimmune hyperthyroidism, which can manifest with a variety of extrathyroidal clinical syndromes such as ophthalmopathy, pretibial myxedema (dermopathy), acropathy, cardiomyopathy, and encephalopathy. In very rare instances, GD can also be diagnosed following severe gastrointestinal symptoms such as dysphagia, heartburn, nausea and vomiting. We hereby describe a rare case of GD with digestive symptoms which w...

ea0037ep627 | Obesity and cardiovascular endocrinology | ECE2015

Irisin/leptin ratio, a biological marker of lean/fat mass, may help to identify LMNA-mutated familial partial lipodystrophies

Bensmaine Faiza , Mapihan Kristell Le , Bourry Samuel , Lion Georges , Vigouroux Corinne , Pigny Pascal , Vantyghem Marie Christine

Irisin is a myokine correlated with lean body mass, despite its association with cardiovascular events (Mantzoros 2014). Increased muscle volume and lipoatrophy have been reported in female FPLD (Ji JCEM 214). Our aim was to determine whether irisin could help to distinguish certain lipodystrophic obesities from FPLD.Methods and patients: Circulating irisin levels (EIA Phoenix) were measured in 20 LMNA-related FPLD, 19 normal-weighed controls (H) and 13 ...

ea0056p765 | Neuroendocrinology | ECE2018

Rathke’s cleft cyst mimiking pituitary apoplexy: a case report

Barka Ines , Bensmaine Faiza , Bah Moctar , Bouche Clara , Gautier Jean Francois

Introduction: The most common sellar lesions are mainly due to pituitary adenomas, craniopharyngiomas and benign cysts. Rathke’s cleft cyst (RCC) is a developmental sellar or suprasellar cystic lesion, which rarely becomes symptomatic. Here, we present an interesting case of intra sellar RCC, with a presenting feature of acute pituitary apoplexy.Case report: A 39 year old healthy women was referred to the emergency room for sudden headache and fatig...

ea0056ep134 | Pituitary and Neuroendocrinology | ECE2018

A case of acromegaly and Cushing’s syndrome

Bensmaine Faiza , Laloie Marie , Barka Ines , Vidal-Trecan Tiphaine , Bouche Clara , Feron Florine , Riveline Jean-Pierre , Gautier Jean-Francois

We herein describe a 55-year-old woman who showed a dramatic improvement in glucose control following treatment for co-existing acromegaly and Cushing’s syndrome. The co-occurrence of acromegaly and Cushing’s syndrome in one individual is extremely rare. This patient was diagnosed as having diabetes mellitus 7 years ago. Afterwards, in spite of insulin therapy, her hyperglycemia could not be well controlled. Endocrinological and radiological examinations revealed sub...