Actualización del tratamiento del síndrome de neoplasia endocrina múltiple tipo 1

Abstract

Introduction: There are different research articles that define multiple endocrine neoplasia type 1, as a syndrome of autosomal dominant inheritance, caused by the MEN1 gene mutation, which is characterized by presenting tumors in endocrine organs such as: entero pancreatic tumors, anterior pituitary tumors and parathyroid tumors. It is very important to know more in depth about this disease, in order to be able to act in the correct way when this clinical picture appears, avoiding complications or death to the patient. Objective: To describe the updated treatment of multiple endocrine neoplasia syndrome type 1, based on a bibliographic review of recent research, increasing the local and regional medical scientific knowledge. Methodology: This research was carried out by collecting information on bibliographic citations of recent years, through scientific research databases such as Google Scholar, Pubmed, Scielo and Dialnet. Conclusion: Definitely this autosomal dominant disease known as multiple endocrine neoplasia type 1 or MEN1, is one of the rarest and most complex pathological entities that exist today, which significantly affects life expectancy in those who suffer from it, likewise from the above mentioned we can say that the updated treatment of choice for people suffering from multiple endocrine neoplasia syndrome type 1 is surgery.