Unexpected extraocular muscle hypoplasia during strabismus surgery: case series.

IF 1.7 4区 医学 Q3 OPHTHALMOLOGY
Yiqing Yuan, Xiying Wang, Ling Ling, Xiaobin Yu, Chao Jiang, Wen Wen, Chen Zhao
{"title":"Unexpected extraocular muscle hypoplasia during strabismus surgery: case series.","authors":"Yiqing Yuan, Xiying Wang, Ling Ling, Xiaobin Yu, Chao Jiang, Wen Wen, Chen Zhao","doi":"10.1186/s12886-024-03787-x","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Reports of congenital isolated medial rectus muscle abnormalities are relatively uncommon and are seldom seen. According to our clinical experience, some rare cases of abnormalities could not be detected by clinical examination and imaging before surgical treatment, which brought difficulties to diagnosis and surgery.</p><p><strong>Case presentation: </strong>In order to provide clinical guidance, we summarized 4 cases with congenital hypoplasia of the medial rectus muscle in our hospital recently. All the patients exhibited exotropia in the primary position. Only one patient (25.0%) exhibited clinically significant limitations of ocular movements. All the patients were identified with congenital hypoplasia of the medial rectus muscle during strabismus surgery; one patient also had hypoplasia of the lateral rectus muscle. However, abnormalities of the rectus muscles were not identified by MRI in three patients (75.0%). In terms of treatment, we enhanced the surgery amount in three patients. Good correction of exotropia was achieved in all patients.</p><p><strong>Conclusions: </strong>Congenital hypoplasia of the medial rectus muscle is extremely rare and some cases are difficult to be detected by clinical examination or imaging. Surgeons should be aware of this condition and should actively but cautiously adjust the surgical parameters based on the patients' intraoperative status.</p>","PeriodicalId":9058,"journal":{"name":"BMC Ophthalmology","volume":"24 1","pages":"517"},"PeriodicalIF":1.7000,"publicationDate":"2024-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11610363/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Ophthalmology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s12886-024-03787-x","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Reports of congenital isolated medial rectus muscle abnormalities are relatively uncommon and are seldom seen. According to our clinical experience, some rare cases of abnormalities could not be detected by clinical examination and imaging before surgical treatment, which brought difficulties to diagnosis and surgery.

Case presentation: In order to provide clinical guidance, we summarized 4 cases with congenital hypoplasia of the medial rectus muscle in our hospital recently. All the patients exhibited exotropia in the primary position. Only one patient (25.0%) exhibited clinically significant limitations of ocular movements. All the patients were identified with congenital hypoplasia of the medial rectus muscle during strabismus surgery; one patient also had hypoplasia of the lateral rectus muscle. However, abnormalities of the rectus muscles were not identified by MRI in three patients (75.0%). In terms of treatment, we enhanced the surgery amount in three patients. Good correction of exotropia was achieved in all patients.

Conclusions: Congenital hypoplasia of the medial rectus muscle is extremely rare and some cases are difficult to be detected by clinical examination or imaging. Surgeons should be aware of this condition and should actively but cautiously adjust the surgical parameters based on the patients' intraoperative status.

斜视手术中意外眼外肌发育不全:病例系列。
背景:先天性孤立性内直肌异常的报道相对罕见,很少见到。根据我们的临床经验,一些罕见的异常病例在手术前的临床检查和影像学检查中无法发现,给诊断和手术带来了困难。病例介绍:总结我院近期收治的4例先天性内直肌发育不全的病例,为临床提供指导。所有患者均表现为主位外斜视。只有1例患者(25.0%)表现出临床上明显的眼球运动限制。所有患者均在斜视手术中确诊为先天性内直肌发育不全;1例患者也有外直肌发育不全。然而,3例(75.0%)患者未通过MRI发现直肌异常。在治疗方面,我们增加了3例患者的手术量。所有患者均获得良好的外斜视矫正。结论:先天性内直肌发育不全极为罕见,部分病例难以通过临床检查或影像学检查发现。外科医生应意识到这种情况,并根据患者术中情况积极而谨慎地调整手术参数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
BMC Ophthalmology
BMC Ophthalmology OPHTHALMOLOGY-
CiteScore
3.40
自引率
5.00%
发文量
441
审稿时长
6-12 weeks
期刊介绍: BMC Ophthalmology is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of eye disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
×
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