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鼻咽部神经胶质异位瘤 - 迷离瘤:病例报告及文献复习

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

作者信息

Baquero-Hoyos Maria Monica, Marino José Antonio, Mayorga José Luis

机构信息

Department of Pediatric Otolaryngology - National Institute of Pediatrics, Mexico City, Mexico.

Attending Physician Department of Pediatric Otolaryngology - National Institute of Pediatrics, Mexico City, Mexico.

出版信息

World J Otorhinolaryngol Head Neck Surg. 2020 Mar 18;7(4):318-321. doi: 10.1016/j.wjorl.2020.02.001. eCollection 2021 Oct.

Abstract

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 non-malignant mass, which may present within a range of symptoms and severity according to its size, growth and location.

摘要

我们描述了一名患有鼻咽错构瘤的9个月大患者的病例。该病例介绍包括对这种病理的病史、放射学、手术和组织学评估的回顾性分析,以及对该实体的文献综述。该病例发生在一名有喂养困难、鼻塞和发育不良的婴儿身上,通过软性鼻内镜检查、CT和MRI进行评估。随后通过手术切除病变,未出现并发症。鼻咽错构瘤是一种罕见的先天性非恶性肿块,根据其大小、生长情况和位置,可能会出现一系列症状和不同的严重程度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c00/8486696/2a35bcd52ca8/gr1.jpg

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