Taiwan Journal of Ophthalmology最新文献

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Bilateral dead bag syndrome in skeletal dysplasia: A case report and review of literature 骨骼发育不良的双侧死袋综合征:病例报告和文献综述
Taiwan Journal of Ophthalmology Pub Date : 2024-01-23 DOI: 10.4103/tjo.tjo-d-23-00088
Prabrisha Banerjee, Sweksha Priya, Sweta Khan, Maitreyi Chowdhury
{"title":"Bilateral dead bag syndrome in skeletal dysplasia: A case report and review of literature","authors":"Prabrisha Banerjee, Sweksha Priya, Sweta Khan, Maitreyi Chowdhury","doi":"10.4103/tjo.tjo-d-23-00088","DOIUrl":"https://doi.org/10.4103/tjo.tjo-d-23-00088","url":null,"abstract":"\u0000 Posterior chamber intraocular lens (IOL) dislocation is a rare yet grave complication of cataract surgery. Late in-the-bag IOL dislocation is usually spontaneous and occurs due to progressive zonular weakness. Aging, high myopia, pseudoexfoliation, vitrectomized eye, and connective tissue disorder are the predisposing factors. A floppy capsular bag without any proliferative deposits has been termed a “dead bag.” Bilateral in-the-bag IOL dislocation or dead bag syndrome is very infrequent. We present such a case in a 67-year-old male with skeletal dysplasia. The patient had undergone uneventful cataract surgery in both eyes 11 years and 6 years ago respectively. Skeletal dysplasia may cause zonulopathy and associated defective collagen synthesis can affect the anchorage points of the zonules. In these patients, cataract surgery should be accomplished by experienced surgeons after detailed counseling of such complications.","PeriodicalId":508969,"journal":{"name":"Taiwan Journal of Ophthalmology","volume":"60 19","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139603001","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
Ophthalmic giant cell arteritis in a patient with normal visual acuity 一名视力正常患者的眼科巨细胞动脉炎
Taiwan Journal of Ophthalmology Pub Date : 2024-01-23 DOI: 10.4103/tjo.tjo-d-23-00082
MacGregor N. Hall, A. Maleki
{"title":"Ophthalmic giant cell arteritis in a patient with normal visual acuity","authors":"MacGregor N. Hall, A. Maleki","doi":"10.4103/tjo.tjo-d-23-00082","DOIUrl":"https://doi.org/10.4103/tjo.tjo-d-23-00082","url":null,"abstract":"\u0000 In this study, we report a case of giant cell arteritis (GCA) and central retinal artery occlusion (CRAO) with cilioretinal artery sparing in a patient who presented with normal visual acuity and was treated with corticosteroids and tocilizumab. An 80-year-old male presented with restriction of his peripheral vision in the right eye along with fever, generalized headache, and jaw pain. His visual acuity was 20/20 in both eyes (OU) with an afferent pupillary defect in the right eye. Dilated fundoscopy revealed whitening of the retina around the vascular arcades with sparing of the central macula in the right eye, indicating CRAO sparing the cilioretinal artery. Laboratory evaluation revealed elevated inflammatory markers. The patient was treated initially with a pulse dose of intravenous corticosteroids, followed by an oral steroid taper, and he underwent a temporal artery biopsy (TAB). At 1-week follow-up, the patient reported improvement in his right eye visual symptoms. The TAB results confirmed the diagnosis of GCA, and the patient’s oral steroid was tapered with the addition of subcutaneous tocilizumab. One month later, the patient’s inflammatory markers returned to normal, and the patient’s vision remained stable. We conclude from this case that GCA may present with normal visual acuity, it can affect the central retinal artery without posterior ciliary artery involvement, and the combination of corticosteroids and subcutaneous tocilizumab may be an adequate treatment regimen.","PeriodicalId":508969,"journal":{"name":"Taiwan Journal of Ophthalmology","volume":"122 9","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139605651","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
Simplified segmental scleral buckling without localization and cryopexy: A retrospective comparison with conventional segmental scleral buckling 无需定位和冷冻的简化节段性巩膜扣锁术:与传统节段式巩膜扣锁术的回顾性比较
Taiwan Journal of Ophthalmology Pub Date : 2024-01-19 DOI: 10.4103/tjo.tjo-d-23-00093
Pei-Hsuan Lin, Yi-An Lee, Lu-Chun Wang
{"title":"Simplified segmental scleral buckling without localization and cryopexy: A retrospective comparison with conventional segmental scleral buckling","authors":"Pei-Hsuan Lin, Yi-An Lee, Lu-Chun Wang","doi":"10.4103/tjo.tjo-d-23-00093","DOIUrl":"https://doi.org/10.4103/tjo.tjo-d-23-00093","url":null,"abstract":"\u0000 \u0000 \u0000 The aim of this study was to propose a simplified segmental scleral buckling (SSSB) technique that does not require break localization for less-experienced vitreoretinal surgeons.\u0000 \u0000 \u0000 \u0000 This retrospective study compared the clinical results of 46 conventional and 23 SSSB (conventional segmental SB [CSSB] and SSSB, respectively) procedures in a tertiary referral retinal center in Taiwan between 2008 and 2019. In the CSSB group, breaks were localized during surgery. In the SSSB group, a wider sponge band and a longer scleral buckle were used to maximize the chances of sealing the retinal breaks based on the preoperative fundus examination findings and to minimize the positioning error caused by cyclotorsion, without performing indirect ophthalmoscopy. The primary outcome was assessed after 6 months. Patient characteristics, surgical parameters, and outcomes were compared between groups. The main outcomes were the duration of surgery, changes in visual acuity, primary success rate, rhegmatogenous retinal detachment recurrence rate, and the frequency of further laser photocoagulation.\u0000 \u0000 \u0000 \u0000 SSSB had a shorter duration than CSSB and was associated with more frequent use of longer and wider explants and need for further laser retinopexy. Both groups showed high primary success rates (95.65%).\u0000 \u0000 \u0000 \u0000 The primary success rates for the SSSB and CSSB groups were comparable and equally high. SSSB required laser retinopexy more frequently and was a shorter procedure.\u0000","PeriodicalId":508969,"journal":{"name":"Taiwan Journal of Ophthalmology","volume":"16 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139612470","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
Endoscopic transmaxillary approach to the inferior rectus muscle in correcting traumatic diplopia 矫正外伤性复视的经下颌直肌内窥镜方法
Taiwan Journal of Ophthalmology Pub Date : 2024-01-16 DOI: 10.4103/tjo.tjo-d-23-00107
Jin-Yu Chang, Yun-Ting Chao, An-Gour Wang, Wei-Kuang Yu
{"title":"Endoscopic transmaxillary approach to the inferior rectus muscle in correcting traumatic diplopia","authors":"Jin-Yu Chang, Yun-Ting Chao, An-Gour Wang, Wei-Kuang Yu","doi":"10.4103/tjo.tjo-d-23-00107","DOIUrl":"https://doi.org/10.4103/tjo.tjo-d-23-00107","url":null,"abstract":"\u0000 Traumatic diplopia can be caused by an entrapped, ruptured, or lost extraocular muscle, which is clinically challenging. Numerous surgical approaches can be tailored, depending on which muscle is involved. We present a patient suffering from inferior rectus muscle disruption treated with endoscopic transmaxillary approach and muscle plication procedure. This surgical technique is a novel and effective surgical technique in managing traumatic diplopia.","PeriodicalId":508969,"journal":{"name":"Taiwan Journal of Ophthalmology","volume":" 49","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139619513","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
Persistent pupillary membrane and accessory iris membrane in cataract surgery 白内障手术中的顽固性瞳孔膜和虹膜附属膜
Taiwan Journal of Ophthalmology Pub Date : 2024-01-16 DOI: 10.4103/tjo.tjo-d-23-00127
Ya-Feng Cheng, Hung-Yu Lin, Shih-Chun Chao
{"title":"Persistent pupillary membrane and accessory iris membrane in cataract surgery","authors":"Ya-Feng Cheng, Hung-Yu Lin, Shih-Chun Chao","doi":"10.4103/tjo.tjo-d-23-00127","DOIUrl":"https://doi.org/10.4103/tjo.tjo-d-23-00127","url":null,"abstract":"\u0000 Incomplete involution of the anterior tunica vasculosa lentis is observed in most newborns, including persistent pupillary membrane (PPM) and accessory iris membrane (AIM). PPM is a common congenital ocular anomaly characterized by delicate iris strands along the pupil. AIM is a rare congenital ocular anomaly characterized by iris tissue strands arising from the iris collarette, forming a pseudopupil. Although most of these membranes do not lead to visual impairment, they can pose challenges during cataract surgery. Our case highlights a unique scenario involving the concurrent presence of PPM and AIM in cataract surgery. The surgeries were performed uneventfully without postoperative complications. To prevent unnecessary interventions and potential disappointment, it is essential to individually assess and plan strategies for patients with either PPM or AIM.","PeriodicalId":508969,"journal":{"name":"Taiwan Journal of Ophthalmology","volume":" 40","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139620066","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
Updates on congenital hereditary endothelial dystrophy 先天性遗传性内皮营养不良症的最新进展
Taiwan Journal of Ophthalmology Pub Date : 2023-11-28 DOI: 10.4103/tjo.tjo-d-23-00135
Neetee Mehta, Anshuman Verma, Divya Sree Achanta, C. Kannabiran, Sanhita Roy, D. Mishra, S. Chaurasia, Deepak P Edward, Muralidhar Ramappa
{"title":"Updates on congenital hereditary endothelial dystrophy","authors":"Neetee Mehta, Anshuman Verma, Divya Sree Achanta, C. Kannabiran, Sanhita Roy, D. Mishra, S. Chaurasia, Deepak P Edward, Muralidhar Ramappa","doi":"10.4103/tjo.tjo-d-23-00135","DOIUrl":"https://doi.org/10.4103/tjo.tjo-d-23-00135","url":null,"abstract":"Congenital hereditary endothelial dystrophy (CHED) is a rare genetic corneal disorder causing progressive cornea clouding and significant visual impairment. CHED remains a leading indication for pediatric corneal transplantation despite its infrequency, particularly in regions with high consanguinity rates like Southeast Asia. Identifying the Solute Carrier Family 4 Member 11 (SLC4A11) gene as the genetic basis of CHED has led to the discovery of it’s various genetic variations. However, a comprehensive understanding of its clinical-genetic correlation, pathophysiology, and optimal management is ongoing. This review aims to consolidate current knowledge about CHED, covering its genetic origins, pathophysiological mechanisms, clinical presentation, and management strategies. Surgical intervention, such as penetrating keratoplasty (PK), Descemet stripping automated endothelial keratoplasty (DSAEK), and Descemet membrane endothelial keratoplasty (DMEK), remains the primary treatment. DSAEK and DMEK offer advantages over PK, including quicker visual recovery, reduced complications, and longer graft survival, especially in the pediatric age group. The timing of surgical interventions depends on disease severity, age at presentation, comorbidities, and visual potential. Elevated oxidative stress in CHED corneal tissue suggests potential benefits from anti-inflammatory drugs to rescue mutated endothelial cells. Considering the limitations of corneal graft surgeries, exploring novel gene-based molecular therapies are essential for future management. Early diagnosis, appropriate surgical interventions, amblyopia control, and genetic counseling for predictive analysis are pivotal for optimizing CHED management. A multidisciplinary approach involving ophthalmologists, researchers, and genetic counselors is essential for precise diagnosis and optimal care for CHED patients.","PeriodicalId":508969,"journal":{"name":"Taiwan Journal of Ophthalmology","volume":"47 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139222232","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
Mucopolysaccharidosis 粘多糖病
Taiwan Journal of Ophthalmology Pub Date : 2023-11-28 DOI: 10.4103/tjo.tjo-d-23-00137
Kusumitha Bhakthaganesh, Manumuraleekrishna, M. Vanathi, S. Ahmed, Noopur Gupta, Radhika Tandon
{"title":"Mucopolysaccharidosis","authors":"Kusumitha Bhakthaganesh, Manumuraleekrishna, M. Vanathi, S. Ahmed, Noopur Gupta, Radhika Tandon","doi":"10.4103/tjo.tjo-d-23-00137","DOIUrl":"https://doi.org/10.4103/tjo.tjo-d-23-00137","url":null,"abstract":"Mucopolysaccharidosis are group of inherited metabolic diseases caused by the absence or malfunctioning of lysosomal enzymes resulting in accumulation of glycosaminoglycans. Over time this accumulation damages cells, tissues, and organs. There are seven types of MPS and 13 subtypes that are associated with multiple organ systems, such as the respiratory, liver, spleen, central nervous systems, arteries, skeletons, eyes, joints, ears, skin, and/or teeth. The various types share some common ocular features that differ in terms of the severity of the affection. Visual loss in MPS patients is varied and can be due to corneal clouding, glaucoma, retinopathy, and optic neuropathy. The primary focus of this review is on changes in the cornea and anterior segment in MPS patients, including clinical and novel investigative modalities, current surgical management, effects of systemic therapy like hematopoietic stem cell transplants (HSCT)and enzyme replacement therapy (ERT), as well as significant research developments.","PeriodicalId":508969,"journal":{"name":"Taiwan Journal of Ophthalmology","volume":"68 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139219308","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
Axenfeld–Rieger syndrome in the pediatric population: A review 小儿阿森费尔德-里格综合征:综述
Taiwan Journal of Ophthalmology Pub Date : 2023-11-24 DOI: 10.4103/tjo.tjo-d-23-00089
Nikhila S. Khandwala, Muralidhar Ramappa, Deepak P Edward, Mehmet C. Mocan
{"title":"Axenfeld–Rieger syndrome in the pediatric population: A review","authors":"Nikhila S. Khandwala, Muralidhar Ramappa, Deepak P Edward, Mehmet C. Mocan","doi":"10.4103/tjo.tjo-d-23-00089","DOIUrl":"https://doi.org/10.4103/tjo.tjo-d-23-00089","url":null,"abstract":"Axenfeld–Rieger syndrome (ARS) is a rare autosomal-dominant neurocristopathy that presents with a variety of classical ocular and systemic findings. The pathophysiology of the disease involves anterior segment dysgenesis, and patients may present with ophthalmic complications early in life, including secondary glaucoma, high refractive errors, amblyopia, and permanent visual damage. There are a limited number of studies in the literature that focus primarily on pediatric patients with ARS. The purpose of this article was to review the current literature on clinical presentation, genetic associations, diagnosis, secondary complications, and treatment of ARS in pediatric patients. Evaluating the essential clinical aspects of the disease in children may allow for earlier diagnosis and treatment and prevent visual morbidity from amblyopia and secondary glaucoma that may result in permanent visual damage.","PeriodicalId":508969,"journal":{"name":"Taiwan Journal of Ophthalmology","volume":"86 8","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139239804","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
Overview of sclerocornea 硬膜病概述
Taiwan Journal of Ophthalmology Pub Date : 2023-11-23 DOI: 10.4103/tjo.tjo-d-23-00070
Rama Rajagopal, Divya Giridhar, Jyotirmay Biswas
{"title":"Overview of sclerocornea","authors":"Rama Rajagopal, Divya Giridhar, Jyotirmay Biswas","doi":"10.4103/tjo.tjo-d-23-00070","DOIUrl":"https://doi.org/10.4103/tjo.tjo-d-23-00070","url":null,"abstract":"Sclerocornea is a rare non-progressive, non-inflammatory usually bilateral congenital corneal opacity that can be associated with both ocular and systemic abnormalities. It could be inherited in 50% of cases. Ill-defined limbal architecture and vascularization in association with ocular comorbidities results in poor outcomes with corneal transplantation. This narrative review summarizes the current literature on etiology and clinical presentation in sclerocornea. With regards to keratoplasty, it focusses on key elements in decision making, highlights the role of investigations and discusses practical surgical pearls to enhance outcome of keratoplasty in these eyes.","PeriodicalId":508969,"journal":{"name":"Taiwan Journal of Ophthalmology","volume":"88 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139243456","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
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