A healthy thirty-seven-year-old male presented with a gunshot injury to the eye. The bullet was lodged in the orbital apex and had caused rupture of the left globe and extensive damage to the orbital soft tissues including the optic nerve, as well as the bones at the apex. This large metallic foreign body needed to be removed as it was causing continuous bleeding and cellulitis; also, its location was precarious. The surgery for tracking and removal of the bullet presented several interesting pointers which are described in this case report.
{"title":"Bullet in the orbital apex: Explosive situation!","authors":"Kamalpreet Likhari","doi":"10.4103/ijo.ijo_7_23","DOIUrl":"https://doi.org/10.4103/ijo.ijo_7_23","url":null,"abstract":"A healthy thirty-seven-year-old male presented with a gunshot injury to the eye. The bullet was lodged in the orbital apex and had caused rupture of the left globe and extensive damage to the orbital soft tissues including the optic nerve, as well as the bones at the apex. This large metallic foreign body needed to be removed as it was causing continuous bleeding and cellulitis; also, its location was precarious. The surgery for tracking and removal of the bullet presented several interesting pointers which are described in this case report.","PeriodicalId":93298,"journal":{"name":"Indian journal of ophthalmology. Case reports","volume":"28 1","pages":"856 - 858"},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75025615","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}
{"title":"Spontaneous appearance and healing of frosted branch angiitis in CMV retinitis","authors":"Ipsita Barman, Vinod Kumar, Sindhuja Kandasamy","doi":"10.4103/ijo.ijo_2969_22","DOIUrl":"https://doi.org/10.4103/ijo.ijo_2969_22","url":null,"abstract":"","PeriodicalId":93298,"journal":{"name":"Indian journal of ophthalmology. Case reports","volume":"49 1","pages":"971 - 971"},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84860807","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}
{"title":"External ophthalmomyiasis caused by larvae of Oestrus ovis","authors":"A. Kaur, D. Mishra, Noel V Sadan","doi":"10.4103/ijo.ijo_45_23","DOIUrl":"https://doi.org/10.4103/ijo.ijo_45_23","url":null,"abstract":"","PeriodicalId":93298,"journal":{"name":"Indian journal of ophthalmology. Case reports","volume":"19 1","pages":"930 - 931"},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81245577","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}
Madhusmita Mahapatra, N. Deori, H. Bhattacharjee, Ankit Ahir
Fundus albipunctatus (FA) is a rare, genetic retinal dystrophy that belongs to a heterogeneous group of genetically determined flecked retina syndromes. The presence of multiple retinal yellowish-white lesions of various sizes and configurations, without vascular or optic nerve abnormalities are characteristic features of these disorders. We report a case of fundus albipunctatus in an Indian girl child born out of consanguineous marriage with a novel homozygous nonsense variation in the RDH5 gene.
{"title":"A rare case of fundus albipunctatus with a novel RDH5 gene mutation","authors":"Madhusmita Mahapatra, N. Deori, H. Bhattacharjee, Ankit Ahir","doi":"10.4103/ijo.ijo_3356_22","DOIUrl":"https://doi.org/10.4103/ijo.ijo_3356_22","url":null,"abstract":"Fundus albipunctatus (FA) is a rare, genetic retinal dystrophy that belongs to a heterogeneous group of genetically determined flecked retina syndromes. The presence of multiple retinal yellowish-white lesions of various sizes and configurations, without vascular or optic nerve abnormalities are characteristic features of these disorders. We report a case of fundus albipunctatus in an Indian girl child born out of consanguineous marriage with a novel homozygous nonsense variation in the RDH5 gene.","PeriodicalId":93298,"journal":{"name":"Indian journal of ophthalmology. Case reports","volume":"35 1","pages":"737 - 738"},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77848090","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}
A. Nagtode, R. Jayagayathri, Liny K Thomas, Y. Dayakar
Warthin tumor is a common and benign salivary gland tumor comprising of 2-15% of all epithelial tumors of the parotid gland. The extra-parotid presentation is seen to be rare at sites like the eyelid, caruncle, and the lacrimal gland. In this study, we have reported an extremely rare case of Warthin cyst of the lacrimal sac in an 82-year-old male patient with swelling over the medial canthal region since the past 2 years.
{"title":"Warthin cyst of lacrimal sac: A rare presentation of a common tumor!","authors":"A. Nagtode, R. Jayagayathri, Liny K Thomas, Y. Dayakar","doi":"10.4103/ijo.ijo_109_23","DOIUrl":"https://doi.org/10.4103/ijo.ijo_109_23","url":null,"abstract":"Warthin tumor is a common and benign salivary gland tumor comprising of 2-15% of all epithelial tumors of the parotid gland. The extra-parotid presentation is seen to be rare at sites like the eyelid, caruncle, and the lacrimal gland. In this study, we have reported an extremely rare case of Warthin cyst of the lacrimal sac in an 82-year-old male patient with swelling over the medial canthal region since the past 2 years.","PeriodicalId":93298,"journal":{"name":"Indian journal of ophthalmology. Case reports","volume":"74 1","pages":"827 - 829"},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75992423","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}
{"title":"13-year-long journey of hyperreflective dots from the internal limiting membrane to posterior hyaloid face amid the evolving posterior vitreous detachment","authors":"Denizcan Özizmirliler, R. Avcı, A. Saatçi","doi":"10.4103/ijo.ijo_2805_22","DOIUrl":"https://doi.org/10.4103/ijo.ijo_2805_22","url":null,"abstract":"","PeriodicalId":93298,"journal":{"name":"Indian journal of ophthalmology. Case reports","volume":"25 1","pages":"970 - 970"},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76046035","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}
Central visual acuity in retinitis pigmentosa (RP) can be compromised by posterior subcapsular cataract, cystoid macular edema, epiretinal membrane, and macular hole formation. However, features like posterior pole neovascularization, central serous chorioretinopathy (CSCR), and proliferative diabetic retinopathy (PDR) are rare in RP. We report three such cases of atypical associations of common retinal diseases in RP that were detected on multimodal imaging.
{"title":"Atypical associations of retinitis pigmentosa: A case series","authors":"S. Lobo, Indu Govindraj, A. Rajendran","doi":"10.4103/ijo.ijo_2973_22","DOIUrl":"https://doi.org/10.4103/ijo.ijo_2973_22","url":null,"abstract":"Central visual acuity in retinitis pigmentosa (RP) can be compromised by posterior subcapsular cataract, cystoid macular edema, epiretinal membrane, and macular hole formation. However, features like posterior pole neovascularization, central serous chorioretinopathy (CSCR), and proliferative diabetic retinopathy (PDR) are rare in RP. We report three such cases of atypical associations of common retinal diseases in RP that were detected on multimodal imaging.","PeriodicalId":93298,"journal":{"name":"Indian journal of ophthalmology. Case reports","volume":"33 1","pages":"739 - 742"},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87470579","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}
Damian García-Teillard, Antonio T Tudela, J. Marquez Estudillo, Pedro B Navarrete, Tatiana Luque
An 86-year-old female patient was treated at home after having suffered a syncopal episode preceded by intermittent dyspnea in the previous weeks. Upon admission, the electrocardiogram showed Mobitz 2 second-degree AV (atrioventricular) block. Our patient suffered from systemic hypertension and chronic open-angle glaucoma, treated, respectively, with losartan 100 mg/hydrochlorthiazise 25 mg every 24 h and timolol 0.5% two times a day (introduced three weeks before after being assessed by ophthalmology service at another hospital center). Dyspnea and electrocardiographic blockage signs stopped once ocular beta blockers (timolol) were discontinued. Ocular topical administration is usually the preferred route for drug supply in ophthalmology and especially in glaucoma treatment, but it is not devoid of interactions and adverse effects. The following clinical case describes how the use of topical beta blockers for the treatment of glaucoma may be at the origin of systemic beta-blockade in our patient, a not so common, yet described situation.
{"title":"It never happens, until it happens","authors":"Damian García-Teillard, Antonio T Tudela, J. Marquez Estudillo, Pedro B Navarrete, Tatiana Luque","doi":"10.4103/ijo.ijo_382_23","DOIUrl":"https://doi.org/10.4103/ijo.ijo_382_23","url":null,"abstract":"An 86-year-old female patient was treated at home after having suffered a syncopal episode preceded by intermittent dyspnea in the previous weeks. Upon admission, the electrocardiogram showed Mobitz 2 second-degree AV (atrioventricular) block. Our patient suffered from systemic hypertension and chronic open-angle glaucoma, treated, respectively, with losartan 100 mg/hydrochlorthiazise 25 mg every 24 h and timolol 0.5% two times a day (introduced three weeks before after being assessed by ophthalmology service at another hospital center). Dyspnea and electrocardiographic blockage signs stopped once ocular beta blockers (timolol) were discontinued. Ocular topical administration is usually the preferred route for drug supply in ophthalmology and especially in glaucoma treatment, but it is not devoid of interactions and adverse effects. The following clinical case describes how the use of topical beta blockers for the treatment of glaucoma may be at the origin of systemic beta-blockade in our patient, a not so common, yet described situation.","PeriodicalId":93298,"journal":{"name":"Indian journal of ophthalmology. Case reports","volume":"85 1","pages":"695 - 696"},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83897035","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}
{"title":"Flower petal imprints in intraocular lenses (IOLs)","authors":"Mousumi Banerjee, B. Mounica, S. Azad","doi":"10.4103/ijo.ijo_550_23","DOIUrl":"https://doi.org/10.4103/ijo.ijo_550_23","url":null,"abstract":"","PeriodicalId":93298,"journal":{"name":"Indian journal of ophthalmology. Case reports","volume":"37 1","pages":"948 - 948"},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90227115","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}
京公网安备 11010802042870号
京ICP备2023020795号-1
扫码关注我们
求助内容：
应助结果提醒方式：