[儿童鼻胶质异位:文献综述和我们自己的一系列观察]。

Q3 Medicine
E V Molodtsova, A S Yunusov, D P Polyakov
{"title":"[儿童鼻胶质异位:文献综述和我们自己的一系列观察]。","authors":"E V Molodtsova, A S Yunusov, D P Polyakov","doi":"10.17116/otorino20259004158","DOIUrl":null,"url":null,"abstract":"<p><p>Nasal glial heterotopia (nasal glioma) is a rare congenital benign accumulation of glial tissue displaced into the nasal cavity or paranasal sinuses.</p><p><strong>Objective: </strong>To analyze our own clinical cases of nasal glioma (features of the clinic, diagnosis and treatment) and compare them with data from foreign literature.</p><p><strong>Material and methods: </strong>A retrospective review of medical histories with a diagnosis of nasal glial heterotopia was conducted from 2017 to November 2023 at the pediatric otorhinolaryngological department of the National Medical Research Center for Otorhinolaryngology. Complaints, anamnesis data, the results of radiation diagnosis and the effectiveness of the treatment were analyzed.</p><p><strong>Result: </strong>Over the past 6 years, 7 patients with a diagnosis of nasal glial heterotopia have been treated in the Department of Pediatric otorhinolaryngology, the average age is 3 years and 8 months ± 3 years and 3 months. Nasal glioma was most often located subcutaneously in 1 patient (14,%), mixed in 1 patient (14.5%), intranasally in 5 patients (71%), in the middle line in 2 patients (14.5%), on the right in 2 patients (28.6%), on the left in 3 patients (42.8%). All patients underwent surgical treatment. External access was used in 1 patient (14.5%), endonasal access was used in 5 patients (71%), and combined access was used in 1 patient (14.5%). Relapses after surgical treatment were not observed in any of the patients from 6 months to 5 years (on average 3 years).</p><p><strong>Conclusion: </strong>Nasal glial heterotopia is a rare congenital pathology. Preoperative examination of the patient is an important moment for determining the preliminary diagnosis, as well as choosing surgical access and for deciding whether to involve a neurosurgeon.</p>","PeriodicalId":23575,"journal":{"name":"Vestnik otorinolaringologii","volume":"90 4","pages":"58"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Nasal glial heterotopia in children: a review of the literature and a series of our own observations].\",\"authors\":\"E V Molodtsova, A S Yunusov, D P Polyakov\",\"doi\":\"10.17116/otorino20259004158\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Nasal glial heterotopia (nasal glioma) is a rare congenital benign accumulation of glial tissue displaced into the nasal cavity or paranasal sinuses.</p><p><strong>Objective: </strong>To analyze our own clinical cases of nasal glioma (features of the clinic, diagnosis and treatment) and compare them with data from foreign literature.</p><p><strong>Material and methods: </strong>A retrospective review of medical histories with a diagnosis of nasal glial heterotopia was conducted from 2017 to November 2023 at the pediatric otorhinolaryngological department of the National Medical Research Center for Otorhinolaryngology. Complaints, anamnesis data, the results of radiation diagnosis and the effectiveness of the treatment were analyzed.</p><p><strong>Result: </strong>Over the past 6 years, 7 patients with a diagnosis of nasal glial heterotopia have been treated in the Department of Pediatric otorhinolaryngology, the average age is 3 years and 8 months ± 3 years and 3 months. Nasal glioma was most often located subcutaneously in 1 patient (14,%), mixed in 1 patient (14.5%), intranasally in 5 patients (71%), in the middle line in 2 patients (14.5%), on the right in 2 patients (28.6%), on the left in 3 patients (42.8%). All patients underwent surgical treatment. External access was used in 1 patient (14.5%), endonasal access was used in 5 patients (71%), and combined access was used in 1 patient (14.5%). Relapses after surgical treatment were not observed in any of the patients from 6 months to 5 years (on average 3 years).</p><p><strong>Conclusion: </strong>Nasal glial heterotopia is a rare congenital pathology. Preoperative examination of the patient is an important moment for determining the preliminary diagnosis, as well as choosing surgical access and for deciding whether to involve a neurosurgeon.</p>\",\"PeriodicalId\":23575,\"journal\":{\"name\":\"Vestnik otorinolaringologii\",\"volume\":\"90 4\",\"pages\":\"58\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Vestnik otorinolaringologii\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.17116/otorino20259004158\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vestnik otorinolaringologii","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17116/otorino20259004158","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

鼻胶质异位(鼻胶质瘤)是一种罕见的先天性良性胶质组织堆积移位到鼻腔或鼻窦。目的:分析我国鼻胶质瘤的临床病例(临床特点、诊断和治疗),并与国外文献资料进行比较。材料与方法:回顾性分析国家耳鼻喉医学研究中心儿童耳鼻喉科2017年至2023年11月诊断为鼻胶质异位的病史。对患者的主诉、记忆资料、放射诊断结果及治疗效果进行分析。结果:6年来儿科耳鼻喉科共收治7例诊断为鼻胶质异位的患者,平均年龄为3岁8个月±3岁3个月。鼻胶质瘤多见于皮下1例(14.%),混合性1例(14.5%),鼻内5例(71%),中线2例(14.5%),右侧2例(28.6%),左侧3例(42.8%)。所有患者均接受手术治疗。1例(14.5%)患者使用外通路,5例(71%)患者使用鼻内通路,1例(14.5%)患者使用联合通路。手术治疗后6个月至5年(平均3年)无复发。结论:鼻胶质异位是一种罕见的先天性病理。术前检查是确定初步诊断的重要时刻,也是选择手术途径和决定是否涉及神经外科医生的重要时刻。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Nasal glial heterotopia in children: a review of the literature and a series of our own observations].

Nasal glial heterotopia (nasal glioma) is a rare congenital benign accumulation of glial tissue displaced into the nasal cavity or paranasal sinuses.

Objective: To analyze our own clinical cases of nasal glioma (features of the clinic, diagnosis and treatment) and compare them with data from foreign literature.

Material and methods: A retrospective review of medical histories with a diagnosis of nasal glial heterotopia was conducted from 2017 to November 2023 at the pediatric otorhinolaryngological department of the National Medical Research Center for Otorhinolaryngology. Complaints, anamnesis data, the results of radiation diagnosis and the effectiveness of the treatment were analyzed.

Result: Over the past 6 years, 7 patients with a diagnosis of nasal glial heterotopia have been treated in the Department of Pediatric otorhinolaryngology, the average age is 3 years and 8 months ± 3 years and 3 months. Nasal glioma was most often located subcutaneously in 1 patient (14,%), mixed in 1 patient (14.5%), intranasally in 5 patients (71%), in the middle line in 2 patients (14.5%), on the right in 2 patients (28.6%), on the left in 3 patients (42.8%). All patients underwent surgical treatment. External access was used in 1 patient (14.5%), endonasal access was used in 5 patients (71%), and combined access was used in 1 patient (14.5%). Relapses after surgical treatment were not observed in any of the patients from 6 months to 5 years (on average 3 years).

Conclusion: Nasal glial heterotopia is a rare congenital pathology. Preoperative examination of the patient is an important moment for determining the preliminary diagnosis, as well as choosing surgical access and for deciding whether to involve a neurosurgeon.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Vestnik otorinolaringologii
Vestnik otorinolaringologii Medicine-Otorhinolaryngology
CiteScore
0.80
自引率
0.00%
发文量
69
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信