Oman Journal of Ophthalmology最新文献

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Atypical presentation of persistent fetal vasculature with Berger's space hemorrhage: Challenges in surgical management. 持续胎儿血管与伯杰氏间隙出血的不典型表现:手术处理的挑战。
Oman Journal of Ophthalmology Pub Date : 2026-02-27 eCollection Date: 2026-01-01 DOI: 10.4103/ojo.ojo_264_22
Sushma Jayanna, Tapas Ranjan Padhi, Komal Agarwal, Subhadra Jalali
{"title":"Atypical presentation of persistent fetal vasculature with Berger's space hemorrhage: Challenges in surgical management.","authors":"Sushma Jayanna, Tapas Ranjan Padhi, Komal Agarwal, Subhadra Jalali","doi":"10.4103/ojo.ojo_264_22","DOIUrl":"10.4103/ojo.ojo_264_22","url":null,"abstract":"<p><p>Persistent fetal vasculature (PFV) with hemorrhage in the Berger's space presents a unique diagnostic and surgical challenge. Description on surgical approaches to such eyes and their outcomes are limited in the literature. We present this case series of three eyes of two babies, with one baby having bilateral presentation, highlight the clinical features, surgical challenges, approach, and surgical tips while operation rare, challenging eyes with atypical PFV.</p>","PeriodicalId":19461,"journal":{"name":"Oman Journal of Ophthalmology","volume":"19 1","pages":"103-106"},"PeriodicalIF":0.0,"publicationDate":"2026-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13043141/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147609545","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
Fungal keratitis treatment: Unveiling strategies and emerging trends - A systematic review. 真菌性角膜炎治疗:揭示策略和新趋势-系统综述。
Oman Journal of Ophthalmology Pub Date : 2026-02-27 eCollection Date: 2026-01-01 DOI: 10.4103/ojo.ojo_67_25
Gabriella Hafidha Badruddin, Stella Nathania, Lukman Edwar
{"title":"Fungal keratitis treatment: Unveiling strategies and emerging trends - A systematic review.","authors":"Gabriella Hafidha Badruddin, Stella Nathania, Lukman Edwar","doi":"10.4103/ojo.ojo_67_25","DOIUrl":"10.4103/ojo.ojo_67_25","url":null,"abstract":"<p><p>This study evaluates the efficacy of antifungal medications for fungal keratitis through a systematic review in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analysis guidelines. A comprehensive search of PubMed, Cochrane, and ScienceDirect was performed, including randomized controlled trials (RCT), cohort, and case-control studies on antifungal therapy for fungal keratitis. Keywords and MeSH terms, including \"keratitis,\" \"fungal keratitis,\" \"antifungal,\" and \"therapy,\" were used to identify relevant studies. The screening process was facilitated through Rayyan, an online-based platform. The inclusion criteria were English-language, full-text human studies on antifungal therapy. Data extraction included study details, interventions, outcomes, and adverse effects, with efficacy evaluated on a scale of 0-2 based on clinical outcomes. Twelve RCT involving 1.715 adult patients from India, China, and Nepal were reviewed. The mean patient age was 48.1 years, with males predominating. All studies used 5% natamycin eye drops, with seven incorporating voriconazole in various forms. Additional therapies included chlorhexidine, amphotericin B, ciprofloxacin, levofloxacin, hypochlorous acid (HOCI), and ketoconazole. Seven studies reported significant improvements in best-corrected visual acuity, infiltrate size, and treatment success. Natamycin monotherapy was shown to have the highest efficacy with a score of 11. Combination therapies, including voriconazole showed effectiveness but with slightly lower scores. In severe cases, combining natamycin with systemic antifungals such as voriconazole, ketoconazole, or amphotericin B was necessary for optimal outcomes.</p>","PeriodicalId":19461,"journal":{"name":"Oman Journal of Ophthalmology","volume":"19 1","pages":"37-47"},"PeriodicalIF":0.0,"publicationDate":"2026-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13043117/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147609616","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
Intracameral perfluoropropane for the management of acute hydrops following keratoconus recurrence in a corneal graft. 眼内全氟丙烷治疗角膜移植术后圆锥角膜复发急性积液。
Oman Journal of Ophthalmology Pub Date : 2026-02-27 eCollection Date: 2026-01-01 DOI: 10.4103/ojo.ojo_422_24
Ritu Arora, Abhilasha Sanoria, Rushad Shroff, Palak Gupta, Apoorva Aggarwal
{"title":"Intracameral perfluoropropane for the management of acute hydrops following keratoconus recurrence in a corneal graft.","authors":"Ritu Arora, Abhilasha Sanoria, Rushad Shroff, Palak Gupta, Apoorva Aggarwal","doi":"10.4103/ojo.ojo_422_24","DOIUrl":"10.4103/ojo.ojo_422_24","url":null,"abstract":"<p><p>Keratoconus is an axial corneal ectasia of obscure etiology. It has been associated with many systemic and ocular diseases as well as with a variety of inheritance patterns. Penetrating keratoplasty (PK) has been highly successful in treating advanced cases. Hydrops within the transplanted material is unusual after PK. We report the two cases of hydrops postkeratoplasty in a keratoconus patient successfully managed with intracameral perfluoropropane injection.</p>","PeriodicalId":19461,"journal":{"name":"Oman Journal of Ophthalmology","volume":"19 1","pages":"133-136"},"PeriodicalIF":0.0,"publicationDate":"2026-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13043152/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147609560","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
Oral cyclophosphamide as part of the treatment regimen in patients with nonparaneoplastic autoimmune retinopathy secondary to birdshot chorioretinopathy. 口服环磷酰胺作为鸟射性脉络膜视网膜病变继发的非副肿瘤性自身免疫性视网膜病变患者治疗方案的一部分
Oman Journal of Ophthalmology Pub Date : 2026-02-27 eCollection Date: 2026-01-01 DOI: 10.4103/ojo.ojo_126_24
Diana Morvey, Arash Maleki, Paula Vivian Tan, C Stephen Foster
{"title":"Oral cyclophosphamide as part of the treatment regimen in patients with nonparaneoplastic autoimmune retinopathy secondary to birdshot chorioretinopathy.","authors":"Diana Morvey, Arash Maleki, Paula Vivian Tan, C Stephen Foster","doi":"10.4103/ojo.ojo_126_24","DOIUrl":"10.4103/ojo.ojo_126_24","url":null,"abstract":"<p><p>The purpose of this case series is to delineate the rationale for employing oral cyclophosphamide along with rituximab in three patients with nonparaneoplastic autoimmune retinopathy (npAIR) secondary to birdshot chorioretinopathy. Case 1: A 50-year-old male with a history of amblyopia in the right eye (OD) presented with floaters and reduced vision in the OD. He was diagnosed with birdshot chorioretinopathy (BSCR) in both eyes (OU). He was successfully treated with cyclosporine and mycophenolate mofetil; however, later, he developed npAIR. He started rituximab infusion and oral cyclophosphamide. After 7 months of treatment, oral cyclophosphamide was stopped due to severe side effects. Case 2: A 58-year-old male presented with an acquired color vision problem in the left eye. He was diagnosed with BSCR in OU. He responded to a clinical trial study for BSCR; however, later, he was diagnosed with npAIR. This patient failed oral cyclophosphamide therapy due to ineffectiveness and side effects. He, subsequently, failed rituximab and bortezomib therapy. Case 3: A 52-year-old female was diagnosed with BSCR. She was successfully treated with mycophenolate mofetil and infliximab for BSCR. She, subsequently, was diagnosed with npAIR, which failed oral cyclophosphamide therapy due to ineffectiveness and side effects and was successfully treated with rituximab and intravenous immunoglobulin infusions. The inclusion of oral cyclophosphamide into the treatment regimen for patients with npAIR secondary to BSCR may raise concerns regarding its safety and efficacy, suggesting the need for careful consideration and evaluation during treatment.</p>","PeriodicalId":19461,"journal":{"name":"Oman Journal of Ophthalmology","volume":"19 1","pages":"92-99"},"PeriodicalIF":0.0,"publicationDate":"2026-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13043124/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147609555","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
Severe panuveitis - Uncommon presentation of cat scratch disease. 严重的全葡萄膜炎-罕见的猫抓病的表现。
Oman Journal of Ophthalmology Pub Date : 2026-02-27 eCollection Date: 2026-01-01 DOI: 10.4103/ojo.ojo_151_23
Sahel-Akmal Che Mohd Hazidi, Abdul-Hadi Rosli, Aidila Jesmin Jabbari
{"title":"Severe panuveitis - Uncommon presentation of cat scratch disease.","authors":"Sahel-Akmal Che Mohd Hazidi, Abdul-Hadi Rosli, Aidila Jesmin Jabbari","doi":"10.4103/ojo.ojo_151_23","DOIUrl":"10.4103/ojo.ojo_151_23","url":null,"abstract":"<p><p>Cat scratch disease (CSD) is a systemic infectious illness caused by the <i>Bartonella henselae</i> and usually transmitted to humans directly through bites, scratches, or licks. The most common posterior segment ocular complication of <i>B. henselae</i> is neuroretinitis. Also reported in the literature are a few unusual retinal presentations including retinal white spots, retinal vasoproliferative lesions, papillitis, macular hole, vitreal detachment, vitritis, and branch retinal artery and venous occlusions. This case report describes a CSD patient who presented with unilateral severe panuveitis. This case highlights another posterior segment presentation of CSD. A 7-year-old boy presented with reduced vision in the right eye for 3 days following cat scratch over the right conjunctiva and lower lid 1 week before. Visual acuity in the right eye was counting finger and the left eye was 6/6. There was no relative afferent papillary defect. The right conjunctiva was mildly injected with healed scar. The intraocular pressure was normal. There was the presence of grade four anterior chamber cells but no hypopyon seen. The right posterior segment showed the presence of vitritis, hyperaemic optic disc swelling, vasculitis, and retinitis lesion. He underwent intravitreal tapping and vancomycin and ceftazidime injection. Subsequently, trans pars plana vitrectomy was performed due to worsening ocular condition and visual acuity (hand movement). The serology investigation was positive for <i>B. henselae</i>. The patient was treated with systemic and topical antibiotics up to 6 weeks. Systemic steroid was added subsequently after the infection was controlled. Following treatment, the ocular inflammations had resolved. The final visual acuity of the right eye was 6/6. Published articles on severe panuveitis as presentation of CSD are extremely limited. A high index of suspicion will facilitate the diagnosis and management, especially in the patient with a history of cat scratch.</p>","PeriodicalId":19461,"journal":{"name":"Oman Journal of Ophthalmology","volume":"19 1","pages":"114-117"},"PeriodicalIF":0.0,"publicationDate":"2026-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13043169/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147608914","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
Myelin oligodendrocyte glycoprotein antibody-associated disease presenting with posterior scleritis. 髓鞘少突胶质细胞糖蛋白抗体相关疾病表现为后巩膜炎。
Oman Journal of Ophthalmology Pub Date : 2026-02-27 eCollection Date: 2026-01-01 DOI: 10.4103/ojo.ojo_300_25
Nisreen Al Balushi, Avital Okrent-Smolar, Sachin Kedar
{"title":"Myelin oligodendrocyte glycoprotein antibody-associated disease presenting with posterior scleritis.","authors":"Nisreen Al Balushi, Avital Okrent-Smolar, Sachin Kedar","doi":"10.4103/ojo.ojo_300_25","DOIUrl":"10.4103/ojo.ojo_300_25","url":null,"abstract":"<p><p>The objective of this article is to describe an unusual presentation of myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) with posterior scleritis and optic neuritis. We report the case of a 50-year-old woman who presented with acute visual deterioration, headache, and painful eye movements. Clinical examination revealed profound vision loss, optic disc edema, and posterior scleritis confirmed via B-scan ultrasound. Magnetic resonance imaging demonstrated optic nerve involvement with perineuritis, and myelin oligodendrocyte glycoprotein antibodies were detected. The patient was treated with intravenous methylprednisolone, oral steroid taper, and plasma exchange, leading to gradual vision recovery. At the 4-month follow-up, she regained functional vision with residual visual field deficits. Ancillary testing confirmed bilateral involvement, despite unilateral symptoms. This case highlights a rare manifestation of MOGAD, suggesting possible inflammatory extension into the scleral tissue. Recognizing posterior scleritis as part of the MOGAD spectrum can aid in timely diagnosis and management.</p>","PeriodicalId":19461,"journal":{"name":"Oman Journal of Ophthalmology","volume":"19 1","pages":"111-113"},"PeriodicalIF":0.0,"publicationDate":"2026-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13043157/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147609590","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
Severe panuveitis - Uncommon presentation of cat scratch disease. 严重的全葡萄膜炎-罕见的猫抓病的表现。
Oman Journal of Ophthalmology Pub Date : 2026-02-27 eCollection Date: 2026-01-01 DOI: 10.4103/ojo.ojo_48_26
Jyotirmay Biswas, Suchitra Pradeep, Anjana Parameswaran
{"title":"Severe panuveitis - Uncommon presentation of cat scratch disease.","authors":"Jyotirmay Biswas, Suchitra Pradeep, Anjana Parameswaran","doi":"10.4103/ojo.ojo_48_26","DOIUrl":"10.4103/ojo.ojo_48_26","url":null,"abstract":"","PeriodicalId":19461,"journal":{"name":"Oman Journal of Ophthalmology","volume":"19 1","pages":"7-8"},"PeriodicalIF":0.0,"publicationDate":"2026-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13043119/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147608889","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
Spontaneously arrested primary congenital glaucoma. 自发性先天性青光眼。
Oman Journal of Ophthalmology Pub Date : 2026-02-27 eCollection Date: 2026-01-01 DOI: 10.4103/ojo.ojo_101_24
Priyasha Goel, Julie Pegu, Suneeta Dubey, Monica Gandhi
{"title":"Spontaneously arrested primary congenital glaucoma.","authors":"Priyasha Goel, Julie Pegu, Suneeta Dubey, Monica Gandhi","doi":"10.4103/ojo.ojo_101_24","DOIUrl":"10.4103/ojo.ojo_101_24","url":null,"abstract":"<p><p>This case report explores a unique instance of primary congenital glaucoma (PCG), where the expected progression was unexpectedly halted without intervention. A 17-year-old female patient presented with diminished vision and left eye exotropia since early childhood. Examination revealed normal right eye vision, but the left eye had significantly reduced visual acuity, manifest exotropia, and megalocornea with Haab striae. Intraocular pressure was within normal range. Anterior segment examination showed prominent iris processes and anterior iris insertion. Fundus examination indicated a healthy optic nerve. Despite initial corneal opacity and megalocornea, there was no current evidence of glaucoma. The diagnosis was spontaneously arrested PCG with amblyopia and sensory exotropia. Genetic analysis revealed a CYP1B1 mutation, emphasizing the variable expressivity associated with this mutation. Regular follow-ups were recommended. This case highlights the complexity and variability of PCG presentations and the need for ongoing monitoring in such cases.</p>","PeriodicalId":19461,"journal":{"name":"Oman Journal of Ophthalmology","volume":"19 1","pages":"143-147"},"PeriodicalIF":0.0,"publicationDate":"2026-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13043168/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147609119","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
The pull of the macula: Optic disc dragging in large macular coloboma. 黄斑的牵拉:大黄斑结肠的视盘牵拉。
Oman Journal of Ophthalmology Pub Date : 2026-02-27 eCollection Date: 2026-01-01 DOI: 10.4103/ojo.ojo_424_24
Sahana S Karanth, Akansha Shetty, K Vaishna
{"title":"The pull of the macula: Optic disc dragging in large macular coloboma.","authors":"Sahana S Karanth, Akansha Shetty, K Vaishna","doi":"10.4103/ojo.ojo_424_24","DOIUrl":"10.4103/ojo.ojo_424_24","url":null,"abstract":"<p><p>Macular coloboma is an excavation at the macula with defective or rudimentary retinal tissue. Here, we present an unusual case of large bilateral macular coloboma with dragging of optic disc. A 48-year-old diabetic male patient presented to our outpatient department with a history of diminution of vision and squint since childhood. Dilated fundus examination revealed bilateral large well-defined excavation at the macula with optic disc displaced temporally and temporal arcade vessels appeared straightened. Rest of the retina was normal. Optical coherence tomography and B-scan ultrasonography findings were consistent with macular coloboma. Association of optic disc dragging and straightened temporal retinal vessels with macular coloboma is a rare entity and aids in exclusion of other differentials.</p>","PeriodicalId":19461,"journal":{"name":"Oman Journal of Ophthalmology","volume":"19 1","pages":"140-142"},"PeriodicalIF":0.0,"publicationDate":"2026-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13043156/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147609357","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
Leber hereditary optic neuropathy triggered by the AstraZeneca coronavirus disease 2019 vaccination. 阿斯利康2019冠状病毒病疫苗引发的Leber遗传性视神经病变。
Oman Journal of Ophthalmology Pub Date : 2026-02-27 eCollection Date: 2026-01-01 DOI: 10.4103/ojo.ojo_431_24
Anan A Aljawi, Nooran Osama Badeeb
{"title":"Leber hereditary optic neuropathy triggered by the AstraZeneca coronavirus disease 2019 vaccination.","authors":"Anan A Aljawi, Nooran Osama Badeeb","doi":"10.4103/ojo.ojo_431_24","DOIUrl":"10.4103/ojo.ojo_431_24","url":null,"abstract":"<p><p>Leber hereditary optic neuropathy (LHON) is a rare mitochondrial disorder primarily affecting young males, characterized by progressive vision loss due to retinal ganglion cell degeneration. LHON is typically associated with specific mitochondrial mutations with potential triggers such as environmental factors and, more recently, postvaccination complications. We present a case of a 35-year-old male who experienced LHON onset 3 weeks following administration of the AstraZeneca Coronavirus disease 2019 vaccine. Despite lacking traditional risk factors, genetic testing confirmed the presence of the mitochondrial genome coding for the NADH-ubiquinone oxidoreductase chain four (MT-ND4) m.11778G >A mutation. The patient's presentation contributed to a delay in diagnosing LHON as demyelinating disease optic neuritis, and after excluding all the possible causes, the diagnosis of postvaccination LHON was considered. Continued vigilance and awareness among healthcare providers are essential for prompt identification and management of LHON in postvaccination contexts.</p>","PeriodicalId":19461,"journal":{"name":"Oman Journal of Ophthalmology","volume":"19 1","pages":"137-139"},"PeriodicalIF":0.0,"publicationDate":"2026-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13043139/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147609562","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
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