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Neovascular Glaucoma Associated with Chronic Rhegmatogenous Retinal Detachment. 慢性孔源性视网膜脱离相关的新生血管性青光眼。
Q3 Medicine Pub Date : 2023-06-01 DOI: 10.3341/kjo.2022.0066
Dong Ik Kim, Min Seok Kim, Se Joon Woo

Purpose: To demonstrate the clinical features and natural course of chronic retinal detachment-associated neovascular glaucoma.

Methods: Ten patients, diagnosed with chronic retinal detachment-associated neovascular glaucoma during 2007-2016 were retrospectively investigated. Besides chronic retinal detachment, no patients had any neovascular glaucoma-predisposing conditions, such as carotid artery disease. Retinal perfusion status was evaluated from the fundus fluorescein angiography images.

Results: The mean age of patients was 57.5 years (range, 22-78 years). Complete retinal reattachment was achieved in three eyes, while partial or total chronic retinal detachment persisted in seven eyes. Wide-angle fundus fluorescein angiography revealed peripheral retinal capillary obstruction and severe nonperfusion. Neovascular glaucoma developed 213.4 months (range, 17-634 months) after retinal detachment. Three eyes received Ahmed valve implantation, while five eyes received intravitreal bevacizumab injection. Intraocular pressure was controlled in 10 eyes. Two eyes developed phthisis bulbi during follow-up.

Conclusions: In eyes with a chronic retinal detachment history, iris neovascularization and neovascular glaucoma can develop due to retinal capillary obstruction and chronic retinal ischemia, even after achieving retinal reattachment. We suggest regular follow-up examinations for patients with chronic retinal detachment, particularly for eyes with retinal nonperfusion, as detected on fundus fluorescein angiography.

目的:探讨慢性视网膜脱离相关性新生血管性青光眼的临床特点及自然病程。方法:回顾性分析2007-2016年诊断为慢性视网膜脱离相关性新生血管性青光眼的10例患者。除慢性视网膜脱离外,没有患者有任何新的血管性青光眼易感条件,如颈动脉疾病。眼底荧光素血管造影评价视网膜灌注状态。结果:患者平均年龄57.5岁(范围22 ~ 78岁)。3只眼视网膜完全复位,7只眼视网膜部分或完全脱离。广角眼底荧光素血管造影显示视网膜周围毛细血管阻塞和严重的非灌注。视网膜脱离后213.4个月(范围17-634个月)发生新生血管性青光眼。3眼接受Ahmed瓣膜植入,5眼接受玻璃体内贝伐单抗注射。控制10眼眼压。随访期间,2只眼出现球皮炎。结论:在有慢性视网膜脱离病史的眼睛中,即使在视网膜再植后,虹膜新生血管和新生血管性青光眼也可能由于视网膜毛细血管阻塞和慢性视网膜缺血而发生。我们建议对慢性视网膜脱离患者进行定期随访检查,特别是对眼底荧光素血管造影检测到的视网膜非灌注的眼睛。
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引用次数: 0
Comparison of Corneal Epithelial Wound Healing between Topical RCI001, Solcoseryl, and Polydeoxyribonucleotide in the Murine Ocular Alkali Burn Model. RCI001、索克瑟利和聚脱氧核糖核苷酸对小鼠眼碱烧伤模型角膜上皮创面愈合的影响。
Q3 Medicine Pub Date : 2023-06-01 DOI: 10.3341/kjo.2023.0019
Myung-Sun Song, Young Ah Ku, Seunghoon Kim, Myung Hee Chung, Yong Ho Kim, Dong Hyun Kim

Purpose: To compare the corneal epithelial wound healing effects of RCI001, Solcoseryl, and polydeoxyribonucleotide (PDRN) in a rat alkali burn model.

Methods: In 40 male Sprague-Dawley rats, we induced alkali burn using filter paper soaked in 0.2N sodium hydroxide. The rats were then treated with topical 0.5% RCI001, 1.0% RCI001, Solcoseryl, or PDRN twice a day for 2 weeks. Corneal epithelial integrity and epithelial healing rate were measured at day 0, 3, 5, 7, 10, and 14. Histologic and immunohistochemistry findings were also assessed.

Results: Both the 0.5% and 1.0% RCI001 groups showed significantly more epithelial healing compared to the control group at day 5, 7, 10, and 14 (each p < 0.05). No statistical difference was found between the 0.5% and 1.0% RCI001 groups. Neither the Solcoseryl nor the PDRN groups showed a significant difference from the control. RCI001 treatment resulted in significantly reduced stromal edema, and a trend towards less inflammatory cell infiltration.

Conclusions: Topical application of RCI001 showed enhanced corneal epithelial wound healing in the murine corneal alkali burn model, presumably by suppressing inflammation. Meanwhile, Solcoseryl and PDRN did not show sufficient therapeutic effects compared to RCI001.

目的:比较RCI001、Solcoseryl和聚脱氧核糖核苷酸(PDRN)对碱烧伤大鼠角膜上皮创面愈合的影响。方法:用滤纸浸泡0.2N氢氧化钠诱导40只雄性sd大鼠碱烧伤。然后用0.5% RCI001, 1.0% RCI001, Solcoseryl或PDRN局部治疗大鼠,每天两次,持续2周。在第0、3、5、7、10和14天测量角膜上皮完整性和上皮愈合率。组织学和免疫组织化学结果也进行了评估。结果:与对照组相比,0.5%和1.0% RCI001组在第5、7、10和14天的上皮愈合均显著增加(p < 0.05)。0.5%和1.0% RCI001组间无统计学差异。与对照组相比,Solcoseryl组和PDRN组均未显示出显著差异。RCI001治疗可显著减少基质水肿,并有减少炎症细胞浸润的趋势。结论:局部应用RCI001可促进小鼠角膜碱烧伤模型角膜上皮创面愈合,可能是通过抑制炎症作用。同时,与RCI001相比,Solcoseryl和PDRN没有表现出足够的治疗效果。
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引用次数: 0
Comparison of Each Eye According to the Order of Noninvasive Keratographic Tear Film Evaluation. 按无创角膜镜泪膜评价顺序的各眼比较。
Q3 Medicine Pub Date : 2023-06-01 DOI: 10.3341/kjo.2022.0135
Haeeun Shin, Soyeon Jung, Ji Won Jung

Purpose: To investigate the effect of order of examination on the results of noninvasive keratograph tear film evaluation using Keratograph5M in dry eye patients.

Methods: One hundred and four patients with dry eye symptoms were analyzed retrospectively. All patients underwent bilateral noninvasive tear film evaluation using measurements of tear meniscus height (TMH) and noninvasive keratograph break-up time (NIKBUT) obtained using Keratograph5M. Measurements were performed sequentially in the order of right TMH, left TMH, right NIKBUT, and left NIKBUT.

Results: There was no statistically significant difference in TMH values between the right and left eyes (0.24 ± 0.08 and 0.23 ± 0.08 mm, respectively). Mean NIKBUT-first (time at first tear film break-up) and mean NIKBUT-average (the mean of all tear film break-up time over the entire cornea) were 6.17 ± 3.28 and 10.00 ± 3.97 seconds, respectively, for right, and 7.43 ± 3.86 and 11.57 ± 4.34 seconds, respectively, for left eyes. In addition, mean NIKBUT-first between right and left eyes, and mean NIKBUT-average between them were statistically significant (p = 0.013 and p = 0.007, respectively). Mean NIKBUT and mean TMH differences were not significantly influenced by right or left eyes, age, or sex (all p > 0.050). Spearman correlation analyses of TMH, NIKBUT-first, and NIKBUT-average results showed moderate positive correlations between right and left eyes (r = 0.470, r = 0.322, and r = 0.576, respectively; p < 0.001).

Conclusions: TMH evaluation was not affected by test order; however, NIKBUT measurement was affected by test order, because of reflex tearing due to forced eye opening during the examination. Therefore, TMH should be evaluated before NIKBUT, and sufficient time interval and caution should be needed between NIKBUT measurements on both eyes.

目的:探讨检查顺序对干眼症患者5m无创角膜摄影泪膜评价结果的影响。方法:回顾性分析104例干眼症患者的临床资料。所有患者均行双侧无创泪膜评估,采用角膜摄影术5m测量撕裂半月板高度(TMH)和无创破裂时间(NIKBUT)。测量顺序为右TMH、左TMH、右NIKBUT、左NIKBUT。结果:左右眼TMH值差异无统计学意义(分别为0.24±0.08 mm和0.23±0.08 mm)。右眼平均NIKBUT-first(泪膜首次破裂时间)和平均NIKBUT-average(全角膜泪膜破裂时间的平均值)分别为6.17±3.28和10.00±3.97秒,左眼分别为7.43±3.86和11.57±4.34秒。左右眼平均NIKBUT-first、左右眼平均NIKBUT-average差异均有统计学意义(p = 0.013、p = 0.007)。平均NIKBUT和平均TMH差异不受左右眼、年龄和性别的显著影响(p > 0.050)。TMH、NIKBUT-first和NIKBUT-average结果的Spearman相关分析显示,右眼和左眼之间存在中度正相关(r = 0.470、r = 0.322和r = 0.576);P < 0.001)。结论:TMH评价不受试验顺序的影响;然而,NIKBUT的测量受到测试顺序的影响,因为在检查过程中由于强迫睁开眼睛而产生反射性撕裂。因此,应在NIKBUT之前评估TMH,并且在NIKBUT测量双眼之间需要足够的时间间隔和谨慎。
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引用次数: 0
Tractional Retinal Detachment in Eyes with Vitreous Hemorrhage and Proliferative Diabetic Retinopathy and Posterior Vitreous Detachment in Fellow Eye. 玻璃体出血伴增殖性糖尿病视网膜病变的牵引性视网膜脱离及同眼玻璃体后脱离。
Q3 Medicine Pub Date : 2023-06-01 DOI: 10.3341/kjo.2022.0161
Chan Woong Joo, Yerim An, Yong-Kyu Kim, Yong Dae Kim, Sung Pyo Park, Kyoung Lae Kim

Purpose: To predict the presence of tractional retinal detachment (TRD) in eyes with dense vitreous hemorrhage (VH) and proliferative diabetic retinopathy (PDR) by evaluating the status of posterior vitreous detachment (PVD) in fellow eyes using optical coherence tomography (OCT).

Methods: A total of 44 eyes from 22 patients who underwent vitrectomy due to dense VH with PDR were enrolled. Using OCT, the PVD status in the fellow eye was divided into two groups (incomplete and complete PVD). The incomplete PVD group included eyes without PVD and eyes with partial PVD. B-scan ultrasonography was performed on eyes with dense VH to evaluate the presence of TRD. Both OCT and B-scan images were reviewed by four ophthalmologists (two novices and two experienced), and the interobserver agreement was evaluated.

Results: There was a difference in the interobserver agreement regarding the presence of TRD in eyes with dense VH evaluated by B scan between novice and experienced ophthalmologists (novice, κ = 0.421 vs. experienced, κ = 0.814), although there was no difference between novice and experienced ophthalmologists in the interobserver agreement regarding the status of PVD in the fellow eye evaluated by OCT (novice, κ = 1.000 vs. experienced, κ = 1.000). All observed TRD during vitrectomy occurred in eyes with incomplete PVD in the fellow eye. Logistic regression analysis revealed a statistically significant relation between TRD and the age of the patient (odds ratio [OR], 0.874; p = 0.047), and between TRD and incomplete PVD in the fellow eye evaluated by OCT (OR, 13.904; p = 0.042).

Conclusions: Evaluation of the PVD status in the fellow eye using OCT may be a useful predictor for detecting the presence of TRD in eyes with dense VH and PDR.

目的:通过光学相干断层扫描(OCT)评估眼后玻璃体脱离(PVD)的状态,预测致密玻璃体出血(VH)和增殖性糖尿病视网膜病变(PDR)患者是否存在牵引性视网膜脱离(TRD)。方法:选取22例玻璃体切除术患者的44只眼作为研究对象。使用OCT将同侧眼PVD状态分为两组(不完全PVD和完全PVD)。不完全PVD组包括无PVD组和部分PVD组。采用b超对有致密VH的眼睛进行检查,以评估是否存在TRD。四名眼科医生(两名新手和两名有经验的)检查了OCT和b扫描图像,并评估了观察者之间的一致性。结果:新手和经验丰富的眼科医生在B扫描评估的致密VH眼是否存在TRD的观察者间一致性上存在差异(新手,κ = 0.421 vs经验丰富,κ = 0.814),尽管新手和经验丰富的眼科医生在OCT评估的同侧眼是否存在PVD的观察者间一致性上没有差异(新手,κ = 1.000 vs经验丰富,κ = 1.000)。玻璃体切除术中观察到的TRD均发生在伴眼不完全性PVD的眼。Logistic回归分析显示,TRD与患者年龄有统计学意义(比值比[OR], 0.874;p = 0.047),另一只眼用OCT评估TRD和不完全PVD之间(OR, 13.904;P = 0.042)。结论:使用OCT评估同侧眼PVD状态可能是检测致密VH和PDR眼是否存在TRD的有效预测因子。
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引用次数: 0
Kimura Disease with Lacrimal Sac and Nasolacrimal Duct Involvement: A Case Report. 木村病伴泪囊及鼻泪管累及1例。
Q3 Medicine Pub Date : 2023-06-01 DOI: 10.3341/kjo.2023.0013
Hyeong Ju Byeon, JaeSang Ko, Jun Yong Kim, Jin Sook Yoon
Dear Editor, Kimura disease (KD) is a rare allergic or autoimmune chronic inflammatory disease of the soft tissue in the head and neck region. Painless subcutaneous masses are presented in the salivary glands, lymph nodes, or deep subcutaneous tissue, which frequently occur in young Asian men. The periocular invasion has been reported in orbit, lacrimal gland, and medial canthus [1,2]. However, the invasion of the nasolacrimal duct along the inside of the lacrimal sac has not been reported. Compared to the angiolymphoid hyperplasia with eosinophilia (ALHE), KD extends to deeper tissue, and when the lacrimal sac or nasolacrimal duct is invaded, epiphora can be the main symptom. Furthermore, in a fibroinf lammatory disease spectrum, immunoglobulin G4-related disease (IgG4-RD) should be differentially diagnosed. Herein, we report a case of KD with lacrimal sac and nasolacrimal duct involvement, along with the differential diagnosis process. Informed consent for publication of the research details and clinical photographs was obtained from the patient. A 64-year-old man presented with enlarged swelling of both his inner canthus accompanied by bilateral tearing for ten months (Fig. 1A). He had no history of surgery or trauma at the periorbital area and only had a medical history of hypertension and hypertensive chronic renal failure. On physical examination, a hard palpable mass at the medial canthus and tear trough area was noted in both eyes, and the lymph nodes behind the ear were palpated. Orbital magnetic resonance image revealed T1-weighted contrast-enhanced soft tissues not only in both medial canthi but also in the lacrimal sac and along nasolacrimal ducts (Fig. 1C, 1D). He underwent an incisional biopsy on the mass at his left medial canthus. In histopathological examination, lymphoid follicles with germinal centers and eosinophilic abscess were formed in the stromal fibrosis, and abundant eosinophils and IgG4 plasma cells were infiltrated (Fig. 1E–1H). Blood samples showed eosinophilia (15.6%; normal range, 0%–7%), elevation in serum IgE level (>5,000 IU/mL; normal range, 0–100 IU/mL), and normal range of serum IgG quantitation (1,253 mg/dL; normal range, 700–1,600 mg/dL) and IgG4 concentrations (1,120 mg/L; normal range, 30–2,010 mg/L). Based on the patient’s clinical features, histological examination, and blood tests, the patient was diagnosed with KD. After the patient was administered 30 mg of prednisolone for a week, the symptoms improved (Fig. 1B), and the steroid was tapered out. The patient in the present report had KD invasion in the lacrimal sac and nasolacrimal duct as well as medial canthus, causing epiphora and palpable masses. For a differential diagnosis with ALHE and IgG4-RD, the location of occurrence, clinical features, histopathology, and serology should be comprehensively considered. Unlike ALHE, which is a benign vascular proliferative tumor manifested as more superficial hemangiomatous papules or nodules on Received: F
{"title":"Kimura Disease with Lacrimal Sac and Nasolacrimal Duct Involvement: A Case Report.","authors":"Hyeong Ju Byeon,&nbsp;JaeSang Ko,&nbsp;Jun Yong Kim,&nbsp;Jin Sook Yoon","doi":"10.3341/kjo.2023.0013","DOIUrl":"https://doi.org/10.3341/kjo.2023.0013","url":null,"abstract":"Dear Editor, Kimura disease (KD) is a rare allergic or autoimmune chronic inflammatory disease of the soft tissue in the head and neck region. Painless subcutaneous masses are presented in the salivary glands, lymph nodes, or deep subcutaneous tissue, which frequently occur in young Asian men. The periocular invasion has been reported in orbit, lacrimal gland, and medial canthus [1,2]. However, the invasion of the nasolacrimal duct along the inside of the lacrimal sac has not been reported. Compared to the angiolymphoid hyperplasia with eosinophilia (ALHE), KD extends to deeper tissue, and when the lacrimal sac or nasolacrimal duct is invaded, epiphora can be the main symptom. Furthermore, in a fibroinf lammatory disease spectrum, immunoglobulin G4-related disease (IgG4-RD) should be differentially diagnosed. Herein, we report a case of KD with lacrimal sac and nasolacrimal duct involvement, along with the differential diagnosis process. Informed consent for publication of the research details and clinical photographs was obtained from the patient. A 64-year-old man presented with enlarged swelling of both his inner canthus accompanied by bilateral tearing for ten months (Fig. 1A). He had no history of surgery or trauma at the periorbital area and only had a medical history of hypertension and hypertensive chronic renal failure. On physical examination, a hard palpable mass at the medial canthus and tear trough area was noted in both eyes, and the lymph nodes behind the ear were palpated. Orbital magnetic resonance image revealed T1-weighted contrast-enhanced soft tissues not only in both medial canthi but also in the lacrimal sac and along nasolacrimal ducts (Fig. 1C, 1D). He underwent an incisional biopsy on the mass at his left medial canthus. In histopathological examination, lymphoid follicles with germinal centers and eosinophilic abscess were formed in the stromal fibrosis, and abundant eosinophils and IgG4 plasma cells were infiltrated (Fig. 1E–1H). Blood samples showed eosinophilia (15.6%; normal range, 0%–7%), elevation in serum IgE level (>5,000 IU/mL; normal range, 0–100 IU/mL), and normal range of serum IgG quantitation (1,253 mg/dL; normal range, 700–1,600 mg/dL) and IgG4 concentrations (1,120 mg/L; normal range, 30–2,010 mg/L). Based on the patient’s clinical features, histological examination, and blood tests, the patient was diagnosed with KD. After the patient was administered 30 mg of prednisolone for a week, the symptoms improved (Fig. 1B), and the steroid was tapered out. The patient in the present report had KD invasion in the lacrimal sac and nasolacrimal duct as well as medial canthus, causing epiphora and palpable masses. For a differential diagnosis with ALHE and IgG4-RD, the location of occurrence, clinical features, histopathology, and serology should be comprehensively considered. Unlike ALHE, which is a benign vascular proliferative tumor manifested as more superficial hemangiomatous papules or nodules on Received: F","PeriodicalId":17883,"journal":{"name":"Korean Journal of Ophthalmology : KJO","volume":"37 3","pages":"281-283"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/75/c2/kjo-2023-0013.PMC10270775.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10017445","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Head Postural Changes in a Child with the Dominant Eye Affected by Superior Oblique Palsy: A Case Report. 上斜肌麻痹影响儿童主眼的头部姿势改变1例。
Q3 Medicine Pub Date : 2023-06-01 DOI: 10.3341/kjo.2022.0143
Taekyoung Woo, Seung Ah Chung
Dear Editor, Patients suffering superior oblique (SO) palsy usually adopt a head tilt contralateral to the affected eye to reduce the hypertropia. However, a paradoxical head tilt ipsilateral to the affected eye is seen in up to 3.4% of patients with SO palsy [1,2]. It is thought that patients with a paradoxical head tilt may prefer increasing image separation or using suppression to maintaining unstable binocular single vision [1–4]. Herein we reported a child with left SO palsy who changed the directions of head tilt when amblyopia developed in the right eye. Written informed consent for publication of the research details and clinical images was obtained from the patient's parents. To the best of our knowledge, this is the first report that found the moment developing a paradoxical head tilt in the unilateral SO palsy. A 4-year-old boy without any trauma or medical history was referred for abnormal head posture. He was born full term with no perinatal history. He previously had a persistent head tilt to the right as shown in video taken at home and whole spine x-ray at the age of 3 years (Fig. 1A, 1B), while there were no abnormal musculoskeletal findings. However, he demonstrated a left head tilt of 15° at the presentation, which was eliminated by patching on the left eye (Fig. 1C, 1D). His best-corrected visual acuity was 20 / 50 in the right eye and 20 / 32 in the left eye with mild hyperopic astigmatism correction (+0.75 +1.25 × 90 for the right eye and +0.50 +0.75 × 90 for the left eye). In primary position, he had a left hypertropia of 6 prism diopters (PD), worsening in the right gaze and on the left head tilt. Versions were consistent with a left SO palsy. Fundus examination showed 8° extorsion in the right eye instead of the left eye, indicating that he preferred the left eye fixation (Fig. 1E, 1F). He started the amblyopia treatment with patching on the left eye. On the patching treatment, he showed a right face turn (Fig. 1G). However, he still showed a left paradoxical head tilt at the age of 5 years when achieving 20 / 20 in both eyes (Fig. 1H). During the 2 years follow-up, he had a left hypertropia of 6 to 8 PD in primary position, that measured 16 PD in the right gaze and orthotropic in the left gaze. The left hypertropia was 10 to 12 PD on the left head tilt and orthotropic on the right head tilt. Ocular motility of the left eye demonstrated +2 overelevation in adduction with –2 underdepression in adduction (Fig. 1I). Worth 4-dot testing revealed a right suppression at 5 m and on the left head tilt while a binocular fusion at 1/3 m. The coronal image of the orbit computed tomography showed symmetric SO muscles in both eyes. He underwent a left inferior oblique myectomy. Intraoperatively, the exaggerated forced ductions testing did not show laxity of the left SO tendon. A month after surgery, he showed improvement in the head position (Fig. 1J). Three months after surgery, he exhibited a mild left head tilt (<5°) with recurrenc
{"title":"Head Postural Changes in a Child with the Dominant Eye Affected by Superior Oblique Palsy: A Case Report.","authors":"Taekyoung Woo,&nbsp;Seung Ah Chung","doi":"10.3341/kjo.2022.0143","DOIUrl":"https://doi.org/10.3341/kjo.2022.0143","url":null,"abstract":"Dear Editor, Patients suffering superior oblique (SO) palsy usually adopt a head tilt contralateral to the affected eye to reduce the hypertropia. However, a paradoxical head tilt ipsilateral to the affected eye is seen in up to 3.4% of patients with SO palsy [1,2]. It is thought that patients with a paradoxical head tilt may prefer increasing image separation or using suppression to maintaining unstable binocular single vision [1–4]. Herein we reported a child with left SO palsy who changed the directions of head tilt when amblyopia developed in the right eye. Written informed consent for publication of the research details and clinical images was obtained from the patient's parents. To the best of our knowledge, this is the first report that found the moment developing a paradoxical head tilt in the unilateral SO palsy. A 4-year-old boy without any trauma or medical history was referred for abnormal head posture. He was born full term with no perinatal history. He previously had a persistent head tilt to the right as shown in video taken at home and whole spine x-ray at the age of 3 years (Fig. 1A, 1B), while there were no abnormal musculoskeletal findings. However, he demonstrated a left head tilt of 15° at the presentation, which was eliminated by patching on the left eye (Fig. 1C, 1D). His best-corrected visual acuity was 20 / 50 in the right eye and 20 / 32 in the left eye with mild hyperopic astigmatism correction (+0.75 +1.25 × 90 for the right eye and +0.50 +0.75 × 90 for the left eye). In primary position, he had a left hypertropia of 6 prism diopters (PD), worsening in the right gaze and on the left head tilt. Versions were consistent with a left SO palsy. Fundus examination showed 8° extorsion in the right eye instead of the left eye, indicating that he preferred the left eye fixation (Fig. 1E, 1F). He started the amblyopia treatment with patching on the left eye. On the patching treatment, he showed a right face turn (Fig. 1G). However, he still showed a left paradoxical head tilt at the age of 5 years when achieving 20 / 20 in both eyes (Fig. 1H). During the 2 years follow-up, he had a left hypertropia of 6 to 8 PD in primary position, that measured 16 PD in the right gaze and orthotropic in the left gaze. The left hypertropia was 10 to 12 PD on the left head tilt and orthotropic on the right head tilt. Ocular motility of the left eye demonstrated +2 overelevation in adduction with –2 underdepression in adduction (Fig. 1I). Worth 4-dot testing revealed a right suppression at 5 m and on the left head tilt while a binocular fusion at 1/3 m. The coronal image of the orbit computed tomography showed symmetric SO muscles in both eyes. He underwent a left inferior oblique myectomy. Intraoperatively, the exaggerated forced ductions testing did not show laxity of the left SO tendon. A month after surgery, he showed improvement in the head position (Fig. 1J). Three months after surgery, he exhibited a mild left head tilt (<5°) with recurrenc","PeriodicalId":17883,"journal":{"name":"Korean Journal of Ophthalmology : KJO","volume":"37 3","pages":"278-280"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a7/7b/kjo-2022-0143.PMC10270776.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10000167","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Correction to: Fractal Dimension of Peripapillary Vasculature in Primary Open-Angle Glaucoma. 原发性开角型青光眼乳头周围血管分形维数的修正。
Q3 Medicine Pub Date : 2023-04-01 DOI: 10.3341/kjo.2022.0089.e1
Chae Hyun Song, Seok Hwan Kim, Kyoung Min Lee
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引用次数: 0
Voretigene Neparvovec for the Treatment of RPE65-associated Retinal Dystrophy: Consensus and Recommendations from the Korea RPE65-IRD Consensus Paper Committee. 用于治疗 RPE65 相关视网膜营养不良症的 Voretigene Neparvovec:韩国 RPE65-IRD 共识文件委员会的共识和建议》。
Q3 Medicine Pub Date : 2023-04-01 Epub Date: 2023-03-23 DOI: 10.3341/kjo.2023.0008
Jinu Han, Kwangsic Joo, Ungsoo Samuel Kim, Se Joon Woo, Eun Kyoung Lee, Joo Yong Lee, Tae Kwann Park, Sang Jin Kim, Suk Ho Byeon

Mutations in the RPE65 gene, associated with Leber congenital amaurosis, early-onset severe retinal dystrophy, and retinitis pigmentosa, gained growing attention since gene therapy for patients with RPE65-associated retinal dystrophy is available in clinical practice. RPE65 gene accounts for a very small proportion of patients with inherited retinal degeneration, especially Asian patients. Because RPE65-associated retinal dystrophy shares common clinical characteristics, such as early-onset severe nyctalopia, nystagmus, low vision, and progressive visual field constriction, with retinitis pigmentosa by other genetic mutations, appropriate genetic testing is essential to make a correct diagnosis. Also, fundus abnormalities can be minimal in early childhood, and the phenotype is highly variable depending on the type of mutations in RPE65-associated retinal dystrophy, which makes a diagnostic difficulty. The aim of this paper is to review the epidemiology of RPE65-associated retinal dystrophy, mutation spectrum, genetic diagnosis, clinical characteristics, and voretigene neparvovec, a gene therapy product for the treatment of RPE65-related retinal dystrophy.

RPE65 基因突变与 Leber 先天性无视力症、早发严重视网膜营养不良症和视网膜色素变性症有关,自临床上对 RPE65 相关视网膜营养不良症患者进行基因治疗以来,该基因突变日益受到关注。在遗传性视网膜变性患者中,RPE65 基因只占很小一部分,尤其是亚洲患者。由于 RPE65 相关性视网膜营养不良症与其他基因突变导致的视网膜色素变性症具有共同的临床特征,如早发性重度夜盲症、眼球震颤、低视力和进行性视野缩窄,因此进行适当的基因检测对做出正确诊断至关重要。此外,眼底异常在儿童早期可能很轻微,表型因 RPE65 相关性视网膜营养不良的突变类型不同而变化很大,这给诊断带来了困难。本文旨在回顾 RPE65 相关性视网膜营养不良症的流行病学、突变谱、基因诊断、临床特征以及用于治疗 RPE65 相关性视网膜营养不良症的基因治疗产品 voretigene neparvovec。
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引用次数: 0
An Atypical Presentation of Optic Disc Melanocytoma: A Case Report. 视盘黑色素细胞瘤的非典型表现1例报告。
Q3 Medicine Pub Date : 2023-04-01 DOI: 10.3341/kjo.2022.0153
Rosa L Pinheiro, Rui B Proença, Maria Cristina F Fonseca
Dear Editor, Optic disc melanocytoma is a unilateral benign tumor of the optic disc. Usually, the optic disc melanocytoma is asymptomatic and remains a stable flat dark pigmented juxtapapillary lesion throughout the patient’s life, and local complications, such as choroidal neovascularization (CNV), have been reported in less than 1% of the cases [1,2]. We describe a case report of a patient with an atypical presentation of an optic disc melanocytoma associated with CNV in which differential diagnosis of a malignant lesion was crucial to avoid unnecessary diagnostic or therapeutic procedures, such as radiotherapy. Informed consent for publication of the research details and clinical images was obtained from the patient. A healthy young man presented with progressive visual loss in the right eye (OD) over 2 months. Visual acuity (VA) was counting fingers in his OD and 20 / 20 in his left eye. Slit-lamp biomicroscopy findings and intraocular pressure were unremarkable bilaterally. Dilated fundoscopy of the OD revealed a peripapillary dark pigmented lesion surrounded by a halo of retinal atrophy, with a slightly elevated nodular portion, near the temporal border (Fig. 1A). There was also a macular edema and two subretinal hemorrhages located inferiorly to the macula. Optical coherence tomography (OCT) of the OD revealed distortion and elevation of the retinal layers towards the nasal macula, as well as an ill-defined subretinal lesion with heterogeneous internal ref lectivity near the optic disc and subretinal f luid (Fig. 1B, 1C). Ultrasonography showed a peripapillary elevated hyperechogenic lesion with a largest basal diameter of 3.18 mm and a thickness of 1.85 mm associated with shallow subretinal fluid (Fig. 1D, 1E). Differential diagnosis of the peripapillary lesion included optic disc melanocytoma with secondary CNV, choroidal melanoma, choroidal nevus, congenital hypertrophy of the retinal pigmented epithelium (CHRPE), and combined hamartoma of retina and retinal pigmented epithelium (RPE). Fine-needle biopsy is seldom necessary to distinguish between benign and malignant tumors, because ultrasound features and clinical examination yield high diagnostic accuracy. The presence of symptoms, subretinal fluid and proximity to the optic nerve are all risk factors predictive of choroidal nevus growth of and transformation into a choroidal melanoma, according to the Collaborative Ocular Melanoma Study (COMS) [3]. However, ultrasound features such as thickness <2 mm and base <5 mm (also according to the COMS), high internal reflectivity, and lack of acoustic hollowness (characteristic of melanoma), along with the juxtapapillary location and patient’s age, suggested a benign pigmented lesion. A combined hamartoma of the retina and RPE was excluded, because combined hamartomas are restricted to the retinal layers and combined hamartomas are usually nonpigmented lesions. On fundoscopy, the lesion could resemble peripapillary CHRPE, except for the lack
{"title":"An Atypical Presentation of Optic Disc Melanocytoma: A Case Report.","authors":"Rosa L Pinheiro,&nbsp;Rui B Proença,&nbsp;Maria Cristina F Fonseca","doi":"10.3341/kjo.2022.0153","DOIUrl":"https://doi.org/10.3341/kjo.2022.0153","url":null,"abstract":"Dear Editor, Optic disc melanocytoma is a unilateral benign tumor of the optic disc. Usually, the optic disc melanocytoma is asymptomatic and remains a stable flat dark pigmented juxtapapillary lesion throughout the patient’s life, and local complications, such as choroidal neovascularization (CNV), have been reported in less than 1% of the cases [1,2]. We describe a case report of a patient with an atypical presentation of an optic disc melanocytoma associated with CNV in which differential diagnosis of a malignant lesion was crucial to avoid unnecessary diagnostic or therapeutic procedures, such as radiotherapy. Informed consent for publication of the research details and clinical images was obtained from the patient. A healthy young man presented with progressive visual loss in the right eye (OD) over 2 months. Visual acuity (VA) was counting fingers in his OD and 20 / 20 in his left eye. Slit-lamp biomicroscopy findings and intraocular pressure were unremarkable bilaterally. Dilated fundoscopy of the OD revealed a peripapillary dark pigmented lesion surrounded by a halo of retinal atrophy, with a slightly elevated nodular portion, near the temporal border (Fig. 1A). There was also a macular edema and two subretinal hemorrhages located inferiorly to the macula. Optical coherence tomography (OCT) of the OD revealed distortion and elevation of the retinal layers towards the nasal macula, as well as an ill-defined subretinal lesion with heterogeneous internal ref lectivity near the optic disc and subretinal f luid (Fig. 1B, 1C). Ultrasonography showed a peripapillary elevated hyperechogenic lesion with a largest basal diameter of 3.18 mm and a thickness of 1.85 mm associated with shallow subretinal fluid (Fig. 1D, 1E). Differential diagnosis of the peripapillary lesion included optic disc melanocytoma with secondary CNV, choroidal melanoma, choroidal nevus, congenital hypertrophy of the retinal pigmented epithelium (CHRPE), and combined hamartoma of retina and retinal pigmented epithelium (RPE). Fine-needle biopsy is seldom necessary to distinguish between benign and malignant tumors, because ultrasound features and clinical examination yield high diagnostic accuracy. The presence of symptoms, subretinal fluid and proximity to the optic nerve are all risk factors predictive of choroidal nevus growth of and transformation into a choroidal melanoma, according to the Collaborative Ocular Melanoma Study (COMS) [3]. However, ultrasound features such as thickness <2 mm and base <5 mm (also according to the COMS), high internal reflectivity, and lack of acoustic hollowness (characteristic of melanoma), along with the juxtapapillary location and patient’s age, suggested a benign pigmented lesion. A combined hamartoma of the retina and RPE was excluded, because combined hamartomas are restricted to the retinal layers and combined hamartomas are usually nonpigmented lesions. On fundoscopy, the lesion could resemble peripapillary CHRPE, except for the lack ","PeriodicalId":17883,"journal":{"name":"Korean Journal of Ophthalmology : KJO","volume":"37 2","pages":"192-194"},"PeriodicalIF":0.0,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/fa/2e/kjo-2022-0153.PMC10151173.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9401654","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparison of Optical Coherence Tomography Biomarkers between Bevacizumab Good Responders and Nonresponders Who were Switched to Dexamethasone Implant in Diabetic Macular Edema. 糖尿病黄斑水肿患者改用地塞米松治疗后,贝伐单抗良好应答者与无应答者的光学相干断层扫描生物标志物比较
Q3 Medicine Pub Date : 2023-04-01 DOI: 10.3341/kjo.2022.0109
Jeong Hyun Lee, Joo Young Shin, Jeeyun Ahn

Purpose: To compare volumetric optical coherence tomography (OCT) biomarkers in bevacizumab responsive and bevacizumab refractory diabetic macular edema (DME) patients switched to the dexamethasone implant to ultimately identify possible prognostic indicators.

Methods: Retrospective analysis of DME patients treated with bevacizumab were done. Patients were divided into those who showed response to bevacizumab (bevacizumab only group) and others who were switched to the dexamethasone implant due to lack of response to bevacizumab (switching group). Volumetric OCT biomarkers such as central macular thickness (CMT), inner and outer cystoid macular edema (CME) volume, serous retinal detachment (SRD) volume, retinal volume (CME + SRD volume) within the 6-mm Early Treatment of Diabetic Retinopathy Study circle were calculated. OCT biomarkers were followed up throughout treatment.

Results: Among total of 144 eyes, 113 patients were included in the bevacizumab only group and 31 patients were included in the switching group. Compared to the bevacizumab only group, the switching group showed higher baseline CMT (558.00 ± 209.60 µm vs. 454.96 ± 125.88 µm, p = 0.003), larger inner CME (6.02 ± 1.43 mm3 vs. 5.12 ± 0.87 mm3, p = 0.004) and SRD volume (0.32 ± 0.40 mm3 vs. 0.11 ± 0.09 mm3, p = 0.015) and higher proportion of patients with SRD (58.06% vs. 31.86%, p = 0.008). In the switching group, CMT, inner CME and SRD volume all showed significant reduction after switching to the dexamethasone implant.

Conclusions: DME with large SRD and inner nuclear layer edema volume may be more effectively treated with the dexamethasone implant than bevacizumab.

目的:比较贝伐珠单抗应答和贝伐珠单抗难治性糖尿病黄斑水肿(DME)患者的体积光学相干断层扫描(OCT)生物标志物,以最终确定可能的预后指标。方法:对使用贝伐单抗治疗的二甲醚患者进行回顾性分析。患者被分为对贝伐单抗有反应的患者(仅贝伐单抗组)和由于对贝伐单抗缺乏反应而改用地塞米松植入物的患者(切换组)。计算6 mm早期糖尿病视网膜病变治疗研究圈内黄斑中央厚度(CMT)、内外囊状黄斑水肿(CME)体积、浆液性视网膜脱离(SRD)体积、视网膜体积(CME + SRD体积)等体积OCT生物标志物。在整个治疗过程中随访OCT生物标志物。结果:144只眼中,仅贝伐单抗组113例,切换组31例。与单一贝伐单抗组相比,切换组的基线CMT(558.00±209.60µm vs. 454.96±125.88µm, p = 0.003)、内CME(6.02±1.43 mm3 vs. 5.12±0.87 mm3, p = 0.004)和SRD体积(0.32±0.40 mm3 vs. 0.11±0.09 mm3, p = 0.015)更高,SRD患者比例(58.06% vs. 31.86%, p = 0.008)更高。切换组CMT、内CME和SRD体积均在切换到地塞米松种植体后显著降低。结论:与贝伐单抗相比,地塞米松植入物治疗SRD大、内核层水肿体积大的二甲醚可能更有效。
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Korean Journal of Ophthalmology : KJO
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