Searchable abstracts of presentations at key conferences in endocrinology

ea0035p542 | Endocrine tumours and neoplasia | ECE2014

Multiple endocrine neoplasia type 1 and 2: a retrospective study

Yaker Fetta , Fedala Soumeya , Chentli Farida , Kabour Samia , Ali Leila Ahmed , Chikouche Mohamed , Griene Lakhdar

Introduction: Multiple endocrine neoplasia (MEN) are rare including MEN1:association of pituitary, pancreatic and parathyroid tumors and MEN 2 regrouping NEM2a: medullary thyroid cancer (MTC), pheochromocytoma and parathyroid tumor and NEM2b with ganglioneuromas. They’re caused by autosomal dominant mutation: MEN1 gene (MEN 1) and RET protooncogen (MEN 2).Aim: Report the phenotypic and evolutionary characteristics of MEN.Popul...

ea0032p508 | Endocrine tumours and neoplasia | ECE2013

Heriditary forms of medullary carcinoma of the thyroid: about a new family

Fedala Nora Soumeya , Chentli Farida , Saraoui Fatima , Griene Lakhdar , Chikouche Mohamed

The medullary carcinoma of thyroid is rare and represent 5–10% of the thyroid cancers. It appears under sporadic and family forms in more than a third of cases. It becomes integrated them into the multiple endocrine neoplasms type 2 of autosomique dominant transmission associate with germinal mutations of the gene RET. We bring report in this study, the observation of a new family shape. BL index case was diagnosed in the age of 42 years further to the appearance of a sev...