{"title":"Acquired Synergistic Divergence: Contrary to Current Literature.","authors":"Martha Waters","doi":"10.22599/bioj.145","DOIUrl":null,"url":null,"abstract":"<p><p>Current literature reports synergistic divergence as a rare, congenital ocular motility pattern associated with adduction palsy. Its mechanism has been likened to Duane's syndrome, and some suggest it be referred to as Duane's Type 4 (Gupta et al. 2010; Schliesser et al. 2016; Wilcox et al. 1981; Khan et al. 2016). There are no published reports of synergistic divergence as an acquired condition, making this case report seemingly the first of its kind. This case report describes an 18-year-old female who presented to clinic in 2013 with symptoms of diplopia and left eye turning outwards. Orthoptic assessment and MRI confirmed a third nerve palsy secondary to cavernous sinus schwannoma. Further monitoring showed progression of the cranial nerve palsy but a stable schwannoma and no aberrant regeneration noted in five years of follow up. The patient was treated with multiple botulinum toxin injections and had squint correction surgery in 2017. Seven months later, synergistic divergence was first noted and remained stable in all following assessments. While the aetiology of acquired synergistic divergence in this case is unclear, we can be confident it is unlikely to be of congenital origin as it was not noted until adulthood and after five years of investigations. This report will discuss possible aetiologies of acquired synergistic divergence and, contrary to current literature, suggest clinicians should consider the possibility that synergistic divergence can be acquired, though is likely to be even rarer than its congenital form.</p>","PeriodicalId":36083,"journal":{"name":"British and Irish Orthoptic Journal","volume":"16 1","pages":"25-28"},"PeriodicalIF":0.0000,"publicationDate":"2020-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510407/pdf/","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"British and Irish Orthoptic Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22599/bioj.145","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: 2
Abstract
Current literature reports synergistic divergence as a rare, congenital ocular motility pattern associated with adduction palsy. Its mechanism has been likened to Duane's syndrome, and some suggest it be referred to as Duane's Type 4 (Gupta et al. 2010; Schliesser et al. 2016; Wilcox et al. 1981; Khan et al. 2016). There are no published reports of synergistic divergence as an acquired condition, making this case report seemingly the first of its kind. This case report describes an 18-year-old female who presented to clinic in 2013 with symptoms of diplopia and left eye turning outwards. Orthoptic assessment and MRI confirmed a third nerve palsy secondary to cavernous sinus schwannoma. Further monitoring showed progression of the cranial nerve palsy but a stable schwannoma and no aberrant regeneration noted in five years of follow up. The patient was treated with multiple botulinum toxin injections and had squint correction surgery in 2017. Seven months later, synergistic divergence was first noted and remained stable in all following assessments. While the aetiology of acquired synergistic divergence in this case is unclear, we can be confident it is unlikely to be of congenital origin as it was not noted until adulthood and after five years of investigations. This report will discuss possible aetiologies of acquired synergistic divergence and, contrary to current literature, suggest clinicians should consider the possibility that synergistic divergence can be acquired, though is likely to be even rarer than its congenital form.
目前的文献报道协同发散是一种罕见的先天性眼运动模式,与内收麻痹相关。其机制被比作Duane综合征,有人建议将其称为Duane's 4型(Gupta et al. 2010;Schliesser et al. 2016;Wilcox et al. 1981;Khan et al. 2016)。目前还没有将协同分化作为一种后天条件的已发表报告,这使得这一病例报告似乎是同类报道中的首例。本病例报告描述了一名18岁女性,于2013年以复视和左眼外翻症状就诊。正视评估和MRI证实第三神经麻痹继发于海绵状窦神经鞘瘤。进一步的监测显示脑神经麻痹的进展,但稳定的神经鞘瘤,并没有异常再生注意到5年的随访。该患者接受了多次肉毒杆菌毒素注射,并于2017年进行了斜视矫正手术。7个月后,首次注意到协同差异,并在所有后续评估中保持稳定。虽然本病例中获得性协同分化的病因尚不清楚,但我们可以确信它不太可能是先天性的,因为直到成年后经过五年的调查才发现。本报告将讨论获得性协同分化的可能病因,并与目前的文献相反,建议临床医生应考虑获得性协同分化的可能性,尽管可能比先天性协同分化更罕见。