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Initial Factors Associated with Resistance to Intravitreal Aflibercept Injection in Polypoidal Choroidal Vasculopathy 多形性脉络膜血管病患者对玻璃体内注射阿弗利百普耐受性的初始相关因素
Pub Date : 2024-07-15 DOI: 10.3341/jkos.2024.65.7.425
Dayoung Moon, Minsub Lee, Hyewon Chung, Hyungwoo Lee
Purpose: To identify initial factors contributing to the resistance against intravitreal aflibercept treatment in polypoidal choroidal vasculopathy (PCV) patients.Methods: This study included PCV patients initially treated with aflibercept. Resistance was defined when treatment did not reduce subretinal fluid (SRF) or intraretinal fluid (IRF) by 100 μm or more after three consecutive 4-week intervals, and the treatment interval could not be extended beyond 8 weeks. To identify initial factors associated with resistance to aflibercept treatment, we examined visual acuity and central choroidal thickness before initial treatment and after three treatments. Choroidal thickness was divided into the thickness of the large choroidal vessel layer and the layer that includes choriocapillaris and medium choroidal vessel thickness (termed medium choroidal vessel/choriocapillaris layer thickness, MCCT). Additionally, the volume of SRF, IRF, subretinal hyperreflective material, and pigment epithelial detachment in optical coherence tomography (OCT) images was investigated. The statistical significance of each factor was assessed through logistic regression analysis.Results: The study included 39 eyes showing no resistance to aflibercept and 37 eyes that exhibited resistance. Multiple logistic regression analysis, adjusted for age and sex, indicated that a lower initial ratio of MCCT to choroidal thickness at the fovea was associated with resistance to aflibercept.Conclusions: In patients with PCV treated with aflibercept, early OCT anatomical structures, such as the initial MCCT-choroidal thickness ratio at the fovea, may predict response to treatment injections.
目的:确定导致多形性脉络膜血管病(PCV)患者对玻璃体内阿弗利百普治疗产生耐药性的初始因素:本研究纳入了最初接受阿弗利百普治疗的PCV患者。当治疗连续三次间隔4周后,视网膜下积液(SRF)或视网膜内积液(IRF)仍未减少100 μm或更多,且治疗间隔不能超过8周时,即定义为耐药。为了确定与阿弗利百普治疗耐药性相关的初始因素,我们检查了初始治疗前和三次治疗后的视力和中心脉络膜厚度。脉络膜厚度分为大脉络膜血管层厚度和包括绒毛膜和中脉络膜血管层厚度(称为中脉络膜血管/绒毛膜层厚度,MCCT)。此外,还对光学相干断层扫描(OCT)图像中的 SRF、IRF、视网膜下高反射物质和色素上皮脱落的体积进行了调查。通过逻辑回归分析评估了各因素的统计学意义:研究包括39只对阿弗利百普无耐药性的眼睛和37只表现出耐药性的眼睛。根据年龄和性别进行调整后的多元逻辑回归分析表明,MCCT与眼窝处脉络膜厚度的初始比值较低与阿弗利百普耐受性有关:结论:在接受阿弗利百普治疗的 PCV 患者中,早期 OCT 解剖结构(如眼窝处的初始 MCCT 与脉络膜厚度比)可预测对治疗注射的反应。
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引用次数: 0
Effects of Cataract on Optic Nerve Head and Macular Analysis Using Optical Coherence Tomography 白内障对视神经头的影响以及使用光学相干断层扫描进行的黄斑分析
Pub Date : 2024-07-15 DOI: 10.3341/jkos.2024.65.7.442
C. Park, Kyoung In Jung
Purpose: To assess the impact of cataract on optic nerve head (ONH) parameters (disc area, rim area, average cup/disc ratio, vertical cup/disc ratio, cup volume), peripapillary retinal nerve fiber layer (pRNFL) thickness, and macular ganglion cell-inner plexiform layer (mGC-IPL) thickness in patients with glaucoma and in a control group.Methods: A retrospective analysis was conducted on medical records from January to December 2021 for individuals undergoing cataract surgery. This group included normal, glaucoma suspects, and glaucoma patients, totaling 44 individuals and 63 eyes. Measurements of ONH parameters, pRNFL thickness, and mGC-IPL thickness were taken using spectral-domain optical coherence tomography before and after surgery. We analyzed postoperative changes in these parameters and related factors to preoperative segmentation errors.Results: In glaucoma patients, a significant increase in the average thickness of the pRNFL (p = 0.002) was observed after surgery, while no significant changes were seen in ONH parameters and the average thickness of the mGC-IPL (all p > 0.05). Conversely, the control group showed an increase in some areas of mGC-IPL thickness after surgery (p < 0.05). Multivariate regression analysis indicated that in glaucoma patients, thinner preoperative pRNFL and mGC-IPL thickness were predictors of increased average thickness after surgery (p < 0.001 and p = 0.008, respectively).Conclusions: Cataract significantly impacts the pRNFL and mGC-IPL thickness in glaucoma patients, with less effect on ONH parameters. These findings suggest that ONH parameters can be more reliable for monitoring patients undergoing cataract surgery and assessing glaucoma progression simultaneously.
目的:评估白内障对青光眼患者和对照组的视神经头(ONH)参数(视盘面积、边缘面积、平均杯/盘比、垂直杯/盘比、杯体积)、毛细血管周围视网膜神经纤维层(pRNFL)厚度和黄斑神经节细胞-内丛状层(mGC-IPL)厚度的影响:我们对 2021 年 1 月至 12 月期间接受白内障手术的病历进行了回顾性分析。该组包括正常人、青光眼疑似患者和青光眼患者,共 44 人 63 眼。我们在手术前后使用光谱域光学相干断层扫描测量了视网膜上皮参数、pRNFL 厚度和 mGC-IPL 厚度。我们分析了术后这些参数的变化以及与术前分割误差相关的因素:结果:在青光眼患者中,术后观察到 pRNFL 平均厚度显著增加(p = 0.002),而 ONH 参数和 mGC-IPL 平均厚度没有显著变化(所有 p > 0.05)。相反,对照组术后某些区域的 mGC-IPL 厚度有所增加(p < 0.05)。多变量回归分析表明,在青光眼患者中,术前较薄的 pRNFL 和 mGC-IPL 厚度是术后平均厚度增加的预测因素(分别为 p < 0.001 和 p = 0.008):结论:白内障对青光眼患者的 pRNFL 和 mGC-IPL 厚度有明显影响,而对 ONH 参数的影响较小。这些研究结果表明,同时监测白内障手术患者和评估青光眼进展,视网膜上皮参数更为可靠。
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引用次数: 0
Changes in Astigmatism after Surgery in Pediatric Patients with Limbal Dermoid 小儿睑外翻患者手术后散光的变化
Pub Date : 2024-07-15 DOI: 10.3341/jkos.2024.65.7.417
Si Young Kim, Ju-Yeun Lee, Ji-Won Kwon
Purpose: To analyze changes in astigmatism and visual acuity in pediatric patients with limbal dermoid before and after surgery.Methods: Twenty-five pediatric patients (7 male, 18 female) diagnosed with limbal dermoid from March 2018 to February 2022 were included. We analyzed best corrected visual acuity and astigmatism using cycloplegic refraction, automated keratometry, and topography before and after surgery.Results: In cycloplegic refraction and automated keratometry, postoperative astigmatism did not decrease significantly (p = 0.53 and p = 0.38, respectively). Topography showed a significant decrease in corneal astigmatism from 3.6 ± 2.8 diopters (D) to 2.7 ± 1.8 D (p < 0.05) and in irregular astigmatism from 3.7 ± 2.2 D to 2.5 ± 1.5 D (p < 0.001). Significant decreases were observed in the corneal irregularity index from 0.14 ± 0.10 mm to 0.08 ± 0.47 mm (p < 0.001) and in the index of surface variance from 60.56 ± 41.02 to 35.00 ± 16.00 (p < 0.001). There was a statistically significant improvement in best corrected visual acuity from logarithm of minimal angle of resolution (logMAR) 0.18 to logMAR 0.07 (p < 0.05).Conclusions: Surgery for limbal dermoid significantly reduced irregular astigmatism and improved best-corrected visual acuity. It is suggested that achieving visual development through active amblyopia treatment after surgery is important.
目的:分析小儿睑缘皮肤瘤患者手术前后散光和视力的变化:纳入2018年3月至2022年2月期间确诊患有瓣膜蝶形的25名儿科患者(7名男性,18名女性)。我们使用环镜屈光、自动角膜计和地形图分析了手术前后的最佳矫正视力和散光:在环视屈光和自动角膜屈光测量中,术后散光没有明显减少(分别为 p = 0.53 和 p = 0.38)。地形图显示,角膜散光从 3.6 ± 2.8 屈光度 (D) 明显降低到 2.7 ± 1.8 屈光度 (P < 0.05),不规则散光从 3.7 ± 2.2 屈光度降低到 2.5 ± 1.5 屈光度 (P < 0.001)。角膜不规则指数从 0.14 ± 0.10 mm 显著下降到 0.08 ± 0.47 mm (p < 0.001),表面差异指数从 60.56 ± 41.02 显著下降到 35.00 ± 16.00 (p < 0.001)。最佳矫正视力从最小解像角对数(logMAR)0.18 到 logMAR 0.07(p < 0.05),有统计学意义:结论:角膜缘结膜瘤手术能显著减少不规则散光,提高最佳矫正视力。结论:角膜缘结膜畸形手术能明显减少不规则散光,提高最佳矫正视力,因此术后通过积极的弱视治疗实现视力发育非常重要。
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引用次数: 0
Correction of Internal Astigmatism Using Toric Scleral Contact Lens after Implantable Collamer Lens Surgery 使用散光巩膜接触镜矫正植入式角膜接触镜手术后的内散光
Pub Date : 2024-07-15 DOI: 10.3341/jkos.2024.65.7.475
S. Yang, Ji Eun Lee
Purpose: We present a case of internal astigmatism correction using a toric scleral contact lens in a patient with high myopia after implantable collamer lens (ICL) surgery.Case summary: A 45-year-old man presented with a significant decrease in visual acuity despite previous ICL surgery. Initial attempts to fit a corneal rigid gas permeable contact lens to the left eye were unsuccessful due to fitting challenges. Subsequently, the use of a spherical scleral contact lens effectively corrected corneal astigmatism but failed to address internal astigmatism, thereby limiting improvement in visual acuity. Postoperative corneal ectasia and ICL rotation were suspected to be the underlying causes of this astigmatism. The introduction of a front toric scleral lens resulted in a significant improvement in visual acuity and sustained comfort throughout the 3-month follow-up period.Conclusions: The use of toric scleral lenses can significantly improve visual acuity and provide exceptional comfort in cases where corneal morphology and lens position change after ICL surgery. This modality presents a promising alternative for future consideration.
目的:我们介绍了一例在植入式角膜接触镜(ICL)手术后使用散光巩膜接触镜矫正高度近视患者内散光的病例。病例摘要:一名 45 岁的男性患者尽管之前接受过 ICL 手术,但视力仍明显下降。由于验配困难,最初尝试为左眼配戴角膜硬性透气接触镜,但没有成功。随后,使用球面巩膜接触镜有效矫正了角膜散光,但未能解决内部散光问题,从而限制了视力的改善。术后角膜异位和 ICL 旋转被怀疑是造成这种散光的根本原因。采用前散光巩膜透镜后,视力得到了显著改善,并在 3 个月的随访期间保持了舒适度:结论:在 ICL 手术后角膜形态和晶状体位置发生变化的情况下,使用散光巩膜透镜可明显改善视力,并提供极佳的舒适度。这种方式是一种很有前途的选择,值得今后考虑。
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引用次数: 0
One-year Clinical Outcome of Topical Bromfenac in Central Serous Chorioretinopathy 外用溴芬酸治疗中心性浆液性脉络膜视网膜病变的一年临床疗效
Pub Date : 2024-07-15 DOI: 10.3341/jkos.2024.65.7.435
Mi Sun Kwon, Yu Min Kim, Jin Young Kim, J. R. Do, Yong Koo Kang, Dong Ho Park
Purpose: To evaluate the efficacy of topical bromfenac in treating central serous chorioretinopathy (CSC) over a 1-year period.Methods: A retrospective analysis was conducted on 57 patients (57 eyes) with CSC followed for > 1 year. Patients were divided into two groups: those treated with bromfenac eye drops twice daily (29 eyes) and a control group (28 eyes). Best-corrected visual acuity (BCVA), central macular thickness (CMT), and subretinal fluid (SRF) height were measured and compared between the two groups as was the proportion of chronic cases.Results: Significant improvements in CMT and SRF height were noted in both groups over the follow-up period. The bromfenac group demonstrated significantly lower CMT at 6, 9, and 12 months (p = 0.045, 0.042, and 0.023, respectively) and lower SRF height (p = 0.037, 0.048, and 0.046, respectively) compared to the control group. The proportion of chronic cases was significantly lower in the bromfenac group (17.2%) compared to the control group (42.9%, p = 0.035).Conclusions: Topical bromfenac reduced the rate of progression to chronic CSC and showed significant anatomical improvements after 6 months, suggesting its potential as an effective treatment option.
目的:评估溴芬酸外用药治疗中心性浆液性脉络膜视网膜病变(CSC)1 年的疗效:对随访超过 1 年的 57 名 CSC 患者(57 只眼)进行回顾性分析。患者被分为两组:每天滴两次溴芬酸眼药水治疗组(29 眼)和对照组(28 眼)。对两组患者的最佳矫正视力(BCVA)、黄斑中心厚度(CMT)和视网膜下积液(SRF)高度进行测量和比较,并比较慢性病例的比例:结果:在随访期间,两组患者的黄斑中心厚度(CMT)和视网膜下积液高度均有显著改善。与对照组相比,溴芬酸钠组在 6、9 和 12 个月时的 CMT 显著降低(p = 0.045、0.042 和 0.023,分别为 0.045、0.042 和 0.023),SRF 高度显著降低(p = 0.037、0.048 和 0.046,分别为 0.037、0.048 和 0.046)。与对照组(42.9%,p = 0.035)相比,溴芬酸组的慢性病例比例(17.2%)明显降低:结论:局部使用溴芬酸可降低慢性 CSC 的进展率,6 个月后在解剖学上也有明显改善,这表明溴芬酸有可能成为一种有效的治疗方案。
{"title":"One-year Clinical Outcome of Topical Bromfenac in Central Serous Chorioretinopathy","authors":"Mi Sun Kwon, Yu Min Kim, Jin Young Kim, J. R. Do, Yong Koo Kang, Dong Ho Park","doi":"10.3341/jkos.2024.65.7.435","DOIUrl":"https://doi.org/10.3341/jkos.2024.65.7.435","url":null,"abstract":"Purpose: To evaluate the efficacy of topical bromfenac in treating central serous chorioretinopathy (CSC) over a 1-year period.Methods: A retrospective analysis was conducted on 57 patients (57 eyes) with CSC followed for > 1 year. Patients were divided into two groups: those treated with bromfenac eye drops twice daily (29 eyes) and a control group (28 eyes). Best-corrected visual acuity (BCVA), central macular thickness (CMT), and subretinal fluid (SRF) height were measured and compared between the two groups as was the proportion of chronic cases.Results: Significant improvements in CMT and SRF height were noted in both groups over the follow-up period. The bromfenac group demonstrated significantly lower CMT at 6, 9, and 12 months (p = 0.045, 0.042, and 0.023, respectively) and lower SRF height (p = 0.037, 0.048, and 0.046, respectively) compared to the control group. The proportion of chronic cases was significantly lower in the bromfenac group (17.2%) compared to the control group (42.9%, p = 0.035).Conclusions: Topical bromfenac reduced the rate of progression to chronic CSC and showed significant anatomical improvements after 6 months, suggesting its potential as an effective treatment option.","PeriodicalId":504314,"journal":{"name":"Journal of the Korean Ophthalmological Society","volume":"4 6","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141646317","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Multiple Evanescent White Dot Syndrome following COVID-19 Vaccination: Two Case Reports 接种 COVID-19 疫苗后的多发性疏散白点综合征:两个病例报告
Pub Date : 2024-07-15 DOI: 10.3341/jkos.2024.65.7.480
Han Eul Lee, Soyeon Jung, Hee Seung Chin
Purpose: We present two cases of multiple evanescent white dot syndrome (MEWDS) following COVID-19 vaccination.Case summary: We present two cases of visual field defects following BNT162b2 (Pfizer-BioNTech, Kronach, Germany) COVID-19 vaccination. A 14-year-old male experienced reduced visual acuity in the temporal field of his left eye after his second dose. Similarly, a 38-year-old woman experienced decreased visual acuity in her right eye after her first dose. Notably, neither patient had pre-existing medical conditions or exhibited COVID-19 symptoms following vaccination. Funduscopic examination revealed multifocal peripapillary hyperreflective lesions in both cases. Visual field defects and hyperreflective lesions spontaneously resolved within 6 weeks, with normal visual acuity and fundus findings at the 7-month follow-up.Conclusions: The recent COVID-19 pandemic has led to a significant increase in vaccination rates. Notably, MEWDS demonstrated a significant association with previous vaccines, including influenza and hepatitis, and the cases describe herein also suggest a potential association between BNT162b2 vaccination and MEWDS.
病例摘要:我们报告了两例接种 BNT162b2(辉瑞生物技术公司,德国克罗纳赫)COVID-19 疫苗后出现视野缺损的病例。一名 14 岁的男性在接种第二剂疫苗后左眼颞叶视野视力下降。同样,一名 38 岁的女性在接种第一剂后也出现了右眼视力下降的情况。值得注意的是,这两名患者在接种疫苗前均未患有疾病,也未出现 COVID-19 症状。眼底检查发现,两例患者均有多灶性毛细血管周围高反射性病变。视野缺损和高反光病变在 6 周内自行消退,7 个月随访时视力和眼底检查结果正常:结论:最近的 COVID-19 大流行使疫苗接种率显著提高。值得注意的是,MEWDS 与以往的疫苗(包括流感疫苗和肝炎疫苗)有显著关联,本文描述的病例也表明 BNT162b2 疫苗接种与 MEWDS 之间可能存在关联。
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引用次数: 0
A Case of Atypical Cytomegalovirus Corneal Endotheliitis after Intravitreal Triamcinolone Injection 一例玻璃体内注射曲安奈德后发生非典型巨细胞病毒角膜内皮炎的病例
Pub Date : 2024-07-15 DOI: 10.3341/jkos.2024.65.7.470
Tae Rim Kim, Min Seok Kang, Bo Kwon Son
Purpose: We present an atypical case of cytomegalovirus corneal endotheliitis after intravitreal triamcinolone injection.Case summary: A 61-year-old man presented with decreased visual acuity after intravitreal triamcinolone (Maqaid®, Wakamoto Pharmaceutical Co., Ltd., Tokyo, Japan) injection for cystoid macular edema following cataract surgery. Ocular examination revealed elevated intraocular pressure, diffuse keratic precipitates with corneal edema, and anterior chamber inflammation. These findings were suggestive of viral corneal endotheliitis. Polymerase chain reaction analysis of the anterior chamber aqueous humor detected cytomegalovirus DNA. Consequently, the patient was diagnosed with cytomegalovirus corneal endotheliitis. He was treated with oral valganciclovir (Valcyte®, Roche, Basel, Switzerland) at a dose of 1,800 mg/day for 3 weeks as an induction phase, followed by 900 mg/day for 3 weeks as a remission phase. This treatment regimen led to significant improvement in corneal edema and anterior chamber inflammation with complete restoration of visual acuity.Conclusions: It is important to note that cytomegalovirus endotheliitis can occur after intravitreal triamcinolone injection and can present in an atypical rather than a typical form.
病例摘要:一名 61 岁的男性因白内障手术后囊样黄斑水肿而在玻璃体内注射曲安奈德(Maqaid®,若本制药株式会社,日本东京)后出现视力下降。眼部检查发现眼压升高、弥漫性角膜沉淀伴角膜水肿和前房发炎。这些结果提示患者患有病毒性角膜内皮炎。前房水的聚合酶链反应分析检测出巨细胞病毒 DNA。因此,患者被诊断为巨细胞病毒性角膜内皮炎。他接受了口服缬更昔洛韦(Valcyte®,罗氏公司,瑞士巴塞尔)治疗,诱导期剂量为每天 1,800 毫克,持续 3 周;缓解期剂量为每天 900 毫克,持续 3 周。这一治疗方案显著改善了角膜水肿和前房炎症,并完全恢复了视力:值得注意的是,巨细胞病毒内皮细胞炎可能会在玻璃体内注射曲安奈德后发生,而且可能表现为非典型而非典型形式。
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引用次数: 0
Clinical Characteristics and Visual Prognosis of Idiopathic Intracranial Hypertension in Korea: A Single-center Experience 韩国特发性颅内高压的临床特征和视觉预后:单中心经验
Pub Date : 2024-07-15 DOI: 10.3341/jkos.2024.65.7.456
Hansol Park, Kyung Ah Park
Purpose: To examine the clinical characteristics, demographic features, and visual prognosis of idiopathic intracranial hypertension (IIH) in Korean patients.Methods: We conducted a retrospective chart review of patients diagnosed with IIH who visited the Neuro-ophthalmology Clinic at Samsung Medical Center from September 2011 to January 2023. This analysis focused on demographic characteristics at onset, clinical manifestations, and visual outcomes at the last follow-up.Results: Out of 34 patients, 20 met the modified Dandy criteria and 14 were presumed to have IIH. The mean age at onset was 32.97 ± 9.6 years with females comprising 85.3% (n = 29) of the sample. The average body mass index (BMI) was 29.15 ± 6.43, with 47.0% of patients (n = 16) classified as obese. The most frequent symptom was headache, reported by 85.3% (n = 29) of patients, followed by pulsatile tinnitus (64.7%, n = 22) and transient visual obscuration (TVO; 32.4%, n = 11). Treatment included observation for 3 patients (8.8%), acetazolamide therapy for 26 patients (76.5%), and ventriculo-peritoneal shunt (V-P shunt) for 2 patients (5.9%). Out of 23 patients with follow-up > 6 months, 87.0%, 8.7%, and 4.3% showed good, fair, and poor visual outcomes, respectively; optic nerve atrophy was observed in 19.6% (9 eyes). The initial peripapillary retinal nerve fiber layer (pRNFL) thickness measured by OCT was 143.56 ± 62.41 μm in the right eye and 139.3 ± 76.38 μm in the left which decreased to 97.39 ± 25.72 and 94.91 ± 19.32 μm, respectively by the last examination.Conclusions: While the proportion of obese patients in this Korean cohort and the average BMI were lower than in western countries, both have increased relative to previous reports from Korea. Most patients experienced a benign course.
目的:研究韩国特发性颅内高压症(IIH)患者的临床特征、人口统计学特征和视觉预后:我们对 2011 年 9 月至 2023 年 1 月在三星医疗中心神经眼科门诊就诊的特发性颅内高压患者进行了回顾性病历审查。分析的重点是发病时的人口统计学特征、临床表现以及最后一次随访时的视力结果:在 34 名患者中,20 人符合修改后的 Dandy 标准,14 人被推测患有 IIH。发病时的平均年龄为(32.97 ± 9.6)岁,女性占样本的 85.3%(n = 29)。平均体重指数(BMI)为(29.15 ± 6.43),47.0%的患者(n = 16)属于肥胖。最常见的症状是头痛,85.3%的患者(29 人)报告了这一症状,其次是搏动性耳鸣(64.7%,22 人)和短暂性视力模糊(TVO;32.4%,11 人)。治疗方法包括对 3 名患者(8.8%)进行观察,对 26 名患者(76.5%)进行乙酰唑胺治疗,对 2 名患者(5.9%)进行脑室腹腔分流术(V-P 分流)。在随访时间超过 6 个月的 23 名患者中,分别有 87.0%、8.7% 和 4.3% 的患者视力预后良好、一般和较差;19.6% 的患者(9 眼)出现视神经萎缩。通过OCT测量的视网膜神经纤维层(pRNFL)初始厚度为右眼(143.56 ± 62.41 μm)和左眼(139.3 ± 76.38 μm),在最后一次检查时分别降至(97.39 ± 25.72)和(94.91 ± 19.32 μm):虽然在这组韩国人中,肥胖患者的比例和平均体重指数低于西方国家,但与韩国以前的报告相比,两者都有所增加。大多数患者的病程为良性。
{"title":"Clinical Characteristics and Visual Prognosis of Idiopathic Intracranial Hypertension in Korea: A Single-center Experience","authors":"Hansol Park, Kyung Ah Park","doi":"10.3341/jkos.2024.65.7.456","DOIUrl":"https://doi.org/10.3341/jkos.2024.65.7.456","url":null,"abstract":"Purpose: To examine the clinical characteristics, demographic features, and visual prognosis of idiopathic intracranial hypertension (IIH) in Korean patients.Methods: We conducted a retrospective chart review of patients diagnosed with IIH who visited the Neuro-ophthalmology Clinic at Samsung Medical Center from September 2011 to January 2023. This analysis focused on demographic characteristics at onset, clinical manifestations, and visual outcomes at the last follow-up.Results: Out of 34 patients, 20 met the modified Dandy criteria and 14 were presumed to have IIH. The mean age at onset was 32.97 ± 9.6 years with females comprising 85.3% (n = 29) of the sample. The average body mass index (BMI) was 29.15 ± 6.43, with 47.0% of patients (n = 16) classified as obese. The most frequent symptom was headache, reported by 85.3% (n = 29) of patients, followed by pulsatile tinnitus (64.7%, n = 22) and transient visual obscuration (TVO; 32.4%, n = 11). Treatment included observation for 3 patients (8.8%), acetazolamide therapy for 26 patients (76.5%), and ventriculo-peritoneal shunt (V-P shunt) for 2 patients (5.9%). Out of 23 patients with follow-up > 6 months, 87.0%, 8.7%, and 4.3% showed good, fair, and poor visual outcomes, respectively; optic nerve atrophy was observed in 19.6% (9 eyes). The initial peripapillary retinal nerve fiber layer (pRNFL) thickness measured by OCT was 143.56 ± 62.41 μm in the right eye and 139.3 ± 76.38 μm in the left which decreased to 97.39 ± 25.72 and 94.91 ± 19.32 μm, respectively by the last examination.Conclusions: While the proportion of obese patients in this Korean cohort and the average BMI were lower than in western countries, both have increased relative to previous reports from Korea. Most patients experienced a benign course.","PeriodicalId":504314,"journal":{"name":"Journal of the Korean Ophthalmological Society","volume":"18 9","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141647725","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Orbital Myositis Leading to Compressive Optic Neuropathy after COVID-19 mRNA Vaccination: A Case Report 接种 COVID-19 mRNA 疫苗后导致压迫性视神经病变的眼眶肌炎:病例报告
Pub Date : 2024-07-15 DOI: 10.3341/jkos.2024.65.7.465
Ji Youn Choi, Kyung In Woo
Purpose: We present a case of bilateral compressive optic neuropathy secondary to orbital myositis after COVID-19 messenger ribonucleic acid (mRNA) vaccination.Case summary: A 51-year-old man developed acute bilateral visual loss and painful ophthalmoplegia shortly after receiving the second dose of the BNT162b2 COVID-19 mRNA vaccine (Comirnaty, Pfizer®, New York, NY, USA). His best-corrected visual acuity was counting fingers at 30 cm and 50 cm in the right and left eyes, respectively. Bilateral eyelid swelling, erythema, conjunctival injection, and color vision deficit were observed. Orbital magnetic resonance imaging revealed diffuse enhancement and hypertrophy of the bilateral extraocular muscles. The patient had no significant ophthalmic history and systemic work-up revealed no evidence of underlying inflammatory disease. Based on the clinical presentation and imaging findings, he was tentatively diagnosed with bilateral compressive optic neuropathy secondary to orbital myositis after COVID-19 mRNA vaccination. He was treated with intravenous corticosteroids for 3 days followed by low-dose oral corticosteroids. One month later, his visual acuity and color vision improved; moreover, the inflammatory signs in the eyelids, conjunctiva, and extraocular muscles resolved. However, after developing COVID-19, he experienced a recurrence of symptoms and was retreated with corticosteroids. Radiotherapy was administered to address persistent color vision deficit in the right eye and recurrent eyelid edema, erythema, and conjunctival injection. This treatment effectively resolved all inflammatory signs and color vision deficits, without signs of recurrence.Conclusions: Acute fulminant orbital myositis with associated compressive optic neuropathy can manifest after COVID-19 mRNA vaccination and onset of COVID-19. Anti-inflammatory treatment measures can effectively control these manifestations.
病例摘要:一名 51 岁的男性在接种第二剂 BNT162b2 COVID-19 mRNA 疫苗(Comirnaty,辉瑞®,美国纽约)后不久出现急性双侧视力下降和眼球疼痛。他左右眼的最佳矫正视力分别为 30 厘米和 50 厘米处数手指。双侧眼睑肿胀、红斑、结膜注射和色觉障碍。眼眶磁共振成像显示双侧眼外肌弥漫性增强和肥厚。患者没有重要的眼科病史,全身检查也没有发现潜在的炎症性疾病。根据临床表现和影像学检查结果,他被初步诊断为接种 COVID-19 mRNA 疫苗后继发眼眶肌炎的双侧压迫性视神经病变。他接受了为期 3 天的静脉皮质类固醇治疗,随后又接受了小剂量口服皮质类固醇治疗。一个月后,他的视力和色觉有所改善,眼睑、结膜和眼外肌的炎症症状也有所缓解。然而,在患上 COVID-19 后,他的症状再次复发,并再次接受皮质类固醇治疗。针对右眼持续性色觉障碍、复发性眼睑水肿、红斑和结膜注射,他接受了放射治疗。这种治疗方法有效地消除了所有炎症症状和色觉障碍,且无复发迹象:结论:COVID-19 mRNA 疫苗接种和发病后可出现急性暴发性眼眶肌炎,并伴有压迫性视神经病变。抗炎治疗措施可有效控制这些表现。
{"title":"Orbital Myositis Leading to Compressive Optic Neuropathy after COVID-19 mRNA Vaccination: A Case Report","authors":"Ji Youn Choi, Kyung In Woo","doi":"10.3341/jkos.2024.65.7.465","DOIUrl":"https://doi.org/10.3341/jkos.2024.65.7.465","url":null,"abstract":"Purpose: We present a case of bilateral compressive optic neuropathy secondary to orbital myositis after COVID-19 messenger ribonucleic acid (mRNA) vaccination.Case summary: A 51-year-old man developed acute bilateral visual loss and painful ophthalmoplegia shortly after receiving the second dose of the BNT162b2 COVID-19 mRNA vaccine (Comirnaty, Pfizer®, New York, NY, USA). His best-corrected visual acuity was counting fingers at 30 cm and 50 cm in the right and left eyes, respectively. Bilateral eyelid swelling, erythema, conjunctival injection, and color vision deficit were observed. Orbital magnetic resonance imaging revealed diffuse enhancement and hypertrophy of the bilateral extraocular muscles. The patient had no significant ophthalmic history and systemic work-up revealed no evidence of underlying inflammatory disease. Based on the clinical presentation and imaging findings, he was tentatively diagnosed with bilateral compressive optic neuropathy secondary to orbital myositis after COVID-19 mRNA vaccination. He was treated with intravenous corticosteroids for 3 days followed by low-dose oral corticosteroids. One month later, his visual acuity and color vision improved; moreover, the inflammatory signs in the eyelids, conjunctiva, and extraocular muscles resolved. However, after developing COVID-19, he experienced a recurrence of symptoms and was retreated with corticosteroids. Radiotherapy was administered to address persistent color vision deficit in the right eye and recurrent eyelid edema, erythema, and conjunctival injection. This treatment effectively resolved all inflammatory signs and color vision deficits, without signs of recurrence.Conclusions: Acute fulminant orbital myositis with associated compressive optic neuropathy can manifest after COVID-19 mRNA vaccination and onset of COVID-19. Anti-inflammatory treatment measures can effectively control these manifestations.","PeriodicalId":504314,"journal":{"name":"Journal of the Korean Ophthalmological Society","volume":"16 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141648812","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Three Familial Cases of Stickler Syndrome: A Case Report 三例家族性 Stickler 综合征病例:病例报告
Pub Date : 2024-07-15 DOI: 10.3341/jkos.2024.65.7.486
Jin Wook Jung, Sung Hyun Ahn, In Cheon You, M. Ahn, Nam-Chun Cho
Purpose: Stickler syndrome, a hereditary connective tissue disorder characterized by mutations in collagen genes, presents with progressive ophthalmopathy and diverse systemic manifestations. Here, we present three familial cases of Stickler syndrome, emphasizing the importance of early detection through clinical investigations and genetic testing.Case summary: Two generations of a family, a mother and her two daughters, were evaluated for Stickler syndrome. All three exhibited bilateral retinal lattice degeneration, perivascular retinal degeneration, and vitreous liquefaction. The daughters shared characteristic facial features, including a flattened face, broad nasal bridge, and micrognathia. Clinical symptoms and examination findings led to diagnoses of Stickler syndrome. Subsequent genetic testing in five family members confirmed a COL2A1 mutation in the three affected individuals.Conclusions: Stickler syndrome carries a high risk of vision loss from ocular complications, necessitating early detection and intervention. In addition, the presence of systemic manifestations, such as musculoskeletal joint disorders, mitral valve prolapse, hearing loss, and cleft palate, emphasizes the importance of prompt detection through appropriate clinical investigations and genetic testing.
目的:Stickler 综合征是一种遗传性结缔组织疾病,其特征是胶原基因突变,表现为进行性眼病和多种全身性表现。在此,我们介绍了三例家族性 Stickler 综合征病例,强调了通过临床检查和基因检测及早发现的重要性。病例摘要:一个家庭的两代人,一位母亲和她的两个女儿,都接受了 Stickler 综合征的评估。三人都表现出双侧视网膜晶格变性、视网膜血管周围变性和玻璃体液化。两个女儿有共同的面部特征,包括脸部扁平、宽鼻梁和小颌畸形。根据临床症状和检查结果,诊断结果为 Stickler 综合征。随后对五名家庭成员进行的基因检测证实,三名患者体内存在 COL2A1 基因突变:结论:斯蒂克勒综合征因眼部并发症导致视力丧失的风险很高,必须及早发现和干预。此外,肌肉骨骼关节紊乱、二尖瓣脱垂、听力损失和腭裂等全身表现的出现,也强调了通过适当的临床检查和基因检测及时发现的重要性。
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引用次数: 0
期刊
Journal of the Korean Ophthalmological Society
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