Nasopharyngeal neuroglial heterotopy-Choristoma:Case report and review of the literature  

作　　者：Maria Monica Baquero-Hoyos JoseAntonio Marino Jose Luis Mayorga 

机构地区：[1]Department of Pediatric Otolaryngology-National Institute of Pediatrics,Mexico City,Mexico [2]Attending Physician Department of Pediatric Otolaryngology-National Institute of Pediatrics,Mexico City,Mexico

出　　处：《World Journal of Otorhinolaryngology-Head and Neck Surgery》2021年第4期318-321,共4页世界耳鼻咽喉头颈外科杂志（英文）

摘　　要：We describe the case of a nine-month-old patient with a nasopharyngeal choristoma.The case presented includes the retrospective review of the historical,radiological,surgical and histological assessment of this pathology as well as a literature review of this entity.This case was presented in an infant with difficulty feeding,nasal obstruction and failure to thrive,evaluated with flexible nasal endoscopy,CT and MRI.The lesion was then surgically removed without complications.Nasopharyngeal choristoma is a rare congenital nonmalignant mass,which may present within a range of symptoms and severity according to its size,growth and location.

关 键 词：CHORISTOMA Neuroglial heterotopy NASOPHARYNX 

分 类 号：R739.63[医药卫生—肿瘤]