Suppr超能文献

神经胶质异位症的一种罕见表现:病例报告

An unusual presentation of neuroglial heterotopia: case report.

作者信息

Karunakaran Parthasarathy, Duraikannu Chary, Pulupula Venkata Narasimha Kumar

机构信息

Department of Radiology, Countess of Chester NHS foundation trust, Chester, United Kingdom.

出版信息

BJR Case Rep. 2020 Sep 29;6(2):20190116. doi: 10.1259/bjrcr.20190116. eCollection 2020 Sep.

Abstract

We report a rare case of nasopharyngeal neuroglial heterotopia in a 16-year-old girl who presented with sore throat and feeling of a lump in her throat. Neuroglial heterotopia is a mass composed of misplaced neural tissue during embryonic development which has lost its intracranial connection. A careful review of literature in PUBMED shows most of the previously reported cases of nasopharyngeal glial heterotopia presented during neonatal or infancy period with symptoms of respiratory distress or airway obstruction. Our case caused a diagnostic dilemma due to late presentation and atypical radiological findings. Imaging, especially MRI, is vital for evaluating such nasopharyngeal masses in children for pre-surgical planning and more importantly to rule out any intracranial communication. Treatment is surgical resection by endoscopic or external approach, with a rare possibility of recurrence.

摘要

我们报告了一例罕见的鼻咽神经胶质异位症,患者为一名16岁女孩,表现为喉咙痛和咽部异物感。神经胶质异位症是一种在胚胎发育过程中由错位的神经组织构成的肿块,已失去其颅内连接。对PUBMED文献的仔细回顾显示,先前报道的大多数鼻咽神经胶质异位症病例出现在新生儿期或婴儿期,伴有呼吸窘迫或气道阻塞症状。我们的病例由于出现较晚和影像学表现不典型而导致诊断困难。影像学检查,尤其是MRI,对于评估儿童此类鼻咽部肿块以进行术前规划至关重要,更重要的是排除任何颅内交通。治疗方法是通过内镜或外部途径进行手术切除,复发可能性很小。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2db6/7527015/aab77e6b7eb2/bjrcr.20190116.g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验