全麻下斜视手术后双侧视神经炎的非典型病例。

IF 0.8 Q4 OPHTHALMOLOGY
Strabismus Pub Date : 2024-06-01 Epub Date: 2024-03-17 DOI:10.1080/09273972.2024.2324166
Himani Pal, Anupam Singh, Sandhya Shrestha, Indar Kumar Sharawat, Prateek Kumar Panda, Barun Kumar
{"title":"全麻下斜视手术后双侧视神经炎的非典型病例。","authors":"Himani Pal, Anupam Singh, Sandhya Shrestha, Indar Kumar Sharawat, Prateek Kumar Panda, Barun Kumar","doi":"10.1080/09273972.2024.2324166","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Strabismus surgery under general anesthesia is a common procedure with rare complications in the form of hemorrhage, infection, slipped muscle, lost muscle, scleral perforation, and anterior segment ischemia. We report a unique case of bilateral optic neuritis following squint surgery under general anesthesia in a 15-year-old girl.</p><p><strong>Methods: </strong>A 15-year-old girl presented with accommodative esotropia with V pattern. She underwent uneventful bilateral inferior oblique recession surgery under general anesthesia with Propofol 60 mg, Atracurium 30 mg, and Fentanyl 70 mcg. On the first post-operative day, the patient had an acute onset of temporal headache which was non-radiating. She responded to supportive treatment and was discharged. However, on the 7th postoperative day, she presented with a constant severe headache in the bitemporal region (left > right) for 3 days. She also experienced a painless diminution of vision for 2 days. There was no vomiting, fever, loose stools, diplopia, difficulty in breathing, peripheral sensation loss, generalized weakness, or bowel/bladder incontinence.</p><p><strong>Results: </strong>The best corrected visual acuity was 6/9 in right eye, and 6/9p in left eye with a relative afferent pupillary defect (RAPD) in the left eye. Both optic discs appeared hyperemic with blurred margins. Magnetic resonance imaging (MRI) of the brain and orbit showed hyperintensity along the intraorbital and intracanalicular parts of bilateral optic nerves on T2 weighted image suggesting bilateral optic neuritis. She received intravenous methylprednisolone pulse therapy followed by oral steroids and responded to the medical treatment with improvement in vision but developed steroid-induced glaucoma requiring medical management over several weeks.</p><p><strong>Discussion: </strong>Neuro-ophthalmic complication in the form of non-arteritic ischemic optic neuropathy has been reported after various ophthalmic surgeries, but bilateral optic neuritis has not been reported to date. This possibility should be kept in mind if any patient presents with similar symptoms. This report also highlights IOP monitoring in pediatric patients receiving systemic steroids to prevent loss of vision due to steroid-induced glaucoma.</p>","PeriodicalId":51700,"journal":{"name":"Strabismus","volume":" ","pages":"102-107"},"PeriodicalIF":0.8000,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"An atypical case of bilateral optic neuritis after strabismus surgery under general anesthesia.\",\"authors\":\"Himani Pal, Anupam Singh, Sandhya Shrestha, Indar Kumar Sharawat, Prateek Kumar Panda, Barun Kumar\",\"doi\":\"10.1080/09273972.2024.2324166\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Strabismus surgery under general anesthesia is a common procedure with rare complications in the form of hemorrhage, infection, slipped muscle, lost muscle, scleral perforation, and anterior segment ischemia. We report a unique case of bilateral optic neuritis following squint surgery under general anesthesia in a 15-year-old girl.</p><p><strong>Methods: </strong>A 15-year-old girl presented with accommodative esotropia with V pattern. She underwent uneventful bilateral inferior oblique recession surgery under general anesthesia with Propofol 60 mg, Atracurium 30 mg, and Fentanyl 70 mcg. On the first post-operative day, the patient had an acute onset of temporal headache which was non-radiating. She responded to supportive treatment and was discharged. However, on the 7th postoperative day, she presented with a constant severe headache in the bitemporal region (left > right) for 3 days. She also experienced a painless diminution of vision for 2 days. There was no vomiting, fever, loose stools, diplopia, difficulty in breathing, peripheral sensation loss, generalized weakness, or bowel/bladder incontinence.</p><p><strong>Results: </strong>The best corrected visual acuity was 6/9 in right eye, and 6/9p in left eye with a relative afferent pupillary defect (RAPD) in the left eye. Both optic discs appeared hyperemic with blurred margins. Magnetic resonance imaging (MRI) of the brain and orbit showed hyperintensity along the intraorbital and intracanalicular parts of bilateral optic nerves on T2 weighted image suggesting bilateral optic neuritis. She received intravenous methylprednisolone pulse therapy followed by oral steroids and responded to the medical treatment with improvement in vision but developed steroid-induced glaucoma requiring medical management over several weeks.</p><p><strong>Discussion: </strong>Neuro-ophthalmic complication in the form of non-arteritic ischemic optic neuropathy has been reported after various ophthalmic surgeries, but bilateral optic neuritis has not been reported to date. This possibility should be kept in mind if any patient presents with similar symptoms. This report also highlights IOP monitoring in pediatric patients receiving systemic steroids to prevent loss of vision due to steroid-induced glaucoma.</p>\",\"PeriodicalId\":51700,\"journal\":{\"name\":\"Strabismus\",\"volume\":\" \",\"pages\":\"102-107\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2024-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Strabismus\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/09273972.2024.2324166\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/3/17 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"OPHTHALMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Strabismus","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/09273972.2024.2324166","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/3/17 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

导言:全身麻醉下的斜视手术是一种常见的手术,其罕见的并发症包括出血、感染、肌肉滑脱、肌肉脱落、巩膜穿孔和眼前节缺血。我们报告了一例15岁女孩在全身麻醉下接受斜视手术后发生双侧视神经炎的独特病例:方法:一名 15 岁女孩出现了 V 型适应性内斜。在丙泊酚 60 毫克、阿曲库铵 30 毫克和芬太尼 70 微克的全身麻醉下,她顺利地接受了双侧下斜肌后退手术。术后第一天,患者出现急性颞部头痛,无放射症状。她接受了支持性治疗后出院。但在术后第 7 天,她出现了持续 3 天的位颞区剧烈头痛(左侧>右侧)。她还经历了 2 天的无痛性视力减退。没有呕吐、发烧、便稀、复视、呼吸困难、周围感觉减退、全身无力或大便/膀胱失禁等症状:最佳矫正视力为右眼6/9,左眼6/9p,左眼有相对传入性瞳孔缺损(RAPD)。两个视盘均出现充血,边缘模糊。脑部和眼眶的磁共振成像(MRI)显示,T2加权图像上双侧视神经沿眶内和椎管内部分呈高密度,提示双侧视神经炎。她接受了静脉甲基强的松龙脉冲治疗,随后口服类固醇,对药物治疗反应良好,视力有所改善,但出现了类固醇诱发的青光眼,需要接受数周的药物治疗:讨论:各种眼科手术后出现非动脉缺血性视神经病变形式的神经眼科并发症已有报道,但双侧视神经炎迄今尚未见报道。如果患者出现类似症状,应牢记这种可能性。本报告还强调了对接受全身性类固醇治疗的儿童患者进行眼压监测,以防止类固醇诱发青光眼导致视力丧失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An atypical case of bilateral optic neuritis after strabismus surgery under general anesthesia.

Introduction: Strabismus surgery under general anesthesia is a common procedure with rare complications in the form of hemorrhage, infection, slipped muscle, lost muscle, scleral perforation, and anterior segment ischemia. We report a unique case of bilateral optic neuritis following squint surgery under general anesthesia in a 15-year-old girl.

Methods: A 15-year-old girl presented with accommodative esotropia with V pattern. She underwent uneventful bilateral inferior oblique recession surgery under general anesthesia with Propofol 60 mg, Atracurium 30 mg, and Fentanyl 70 mcg. On the first post-operative day, the patient had an acute onset of temporal headache which was non-radiating. She responded to supportive treatment and was discharged. However, on the 7th postoperative day, she presented with a constant severe headache in the bitemporal region (left > right) for 3 days. She also experienced a painless diminution of vision for 2 days. There was no vomiting, fever, loose stools, diplopia, difficulty in breathing, peripheral sensation loss, generalized weakness, or bowel/bladder incontinence.

Results: The best corrected visual acuity was 6/9 in right eye, and 6/9p in left eye with a relative afferent pupillary defect (RAPD) in the left eye. Both optic discs appeared hyperemic with blurred margins. Magnetic resonance imaging (MRI) of the brain and orbit showed hyperintensity along the intraorbital and intracanalicular parts of bilateral optic nerves on T2 weighted image suggesting bilateral optic neuritis. She received intravenous methylprednisolone pulse therapy followed by oral steroids and responded to the medical treatment with improvement in vision but developed steroid-induced glaucoma requiring medical management over several weeks.

Discussion: Neuro-ophthalmic complication in the form of non-arteritic ischemic optic neuropathy has been reported after various ophthalmic surgeries, but bilateral optic neuritis has not been reported to date. This possibility should be kept in mind if any patient presents with similar symptoms. This report also highlights IOP monitoring in pediatric patients receiving systemic steroids to prevent loss of vision due to steroid-induced glaucoma.

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
Strabismus
Strabismus OPHTHALMOLOGY-
CiteScore
1.60
自引率
11.10%
发文量
30
×
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:481959085
Book学术官方微信