Intranasal glial heterotopia in an infant boy

作     者：Wei Zhang Lixing Tang Wentong Ge Zhang Wei;Tang Lixing;Ge Wentong

作者机构：Department of OtorhinolaryngologyHead and Neck SurgeryBeijing Children’s HospitalCapital Medical UniversityNational Center for Children’s HealthBeijingChina 

出 版 物：《Pediatric Investigation》 (儿科学研究（英文）)

年 卷 期：2021年第5卷第1期

页      面：69-72页

核心收录：

学科分类：1004[医学-公共卫生与预防医学(可授医学、理学学位)] 1002[医学-临床医学] 100213[医学-耳鼻咽喉科学] 10[医学] 

主　　题：Intranasal Glial heterotopia Infant Encephalocele 

摘      要：Introduction:Nasal glial heterotopia is a rare congenital developmental disorder characterized by meningeal epithelium and/or glial *** presentation:A 2-month-old boy presented for treatment of a congenital mass in the right nasal cavity near the *** preoperative diagnosis was congenital intranasal *** endoscopic resection of the nasopharyngeal mass was performed under general *** findings in the resected tissue supported a diagnosis of intranasal glial *** surgical outcome was good and no surgical site infection *** 1 year of follow-up,the patient did not exhibit recurrence of heterotopia or related ***:Transnasal endoscopic surgery is recommended for patients with intranasal glial *** preoperative imaging should be performed before glioma *** mass should be differentiated from encephalocele to prevent cerebrospinal fluid leakage and meningitis.