Case Reports in Ophthalmological Medicine最新文献

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Neovascular Glaucoma from Ocular Ischemic Syndrome Treated with Serial Monthly Intravitreal Bevacizumab and Panretinal Photocoagulation: A Case Report. 连续每月玻璃体内贝伐单抗和全视网膜光凝治疗缺血性青光眼一例报告。
IF 0.9
Case Reports in Ophthalmological Medicine Pub Date : 2022-07-28 eCollection Date: 2022-01-01 DOI: 10.1155/2022/4959522
Hassaan Asif, Zhuangjun Si, Steven Quan, Pathik Amin, David Dao, Lincoln Shaw, Dimitra Skondra, Mary Qiu
{"title":"Neovascular Glaucoma from Ocular Ischemic Syndrome Treated with Serial Monthly Intravitreal Bevacizumab and Panretinal Photocoagulation: A Case Report.","authors":"Hassaan Asif,&nbsp;Zhuangjun Si,&nbsp;Steven Quan,&nbsp;Pathik Amin,&nbsp;David Dao,&nbsp;Lincoln Shaw,&nbsp;Dimitra Skondra,&nbsp;Mary Qiu","doi":"10.1155/2022/4959522","DOIUrl":"https://doi.org/10.1155/2022/4959522","url":null,"abstract":"<p><strong>Purpose: </strong>To describe a case of open-angle neovascular glaucoma (NVG) secondary to ocular ischemic syndrome (OIS) treated with a planned series of 6 monthly anti-VEGF injections with interspersed panretinal photocoagulation (PRP) sessions. We term this treatment protocol the Salvaging Conventional Outflow Pathway in Neovascular Glaucoma (SCOPING) Protocol, and this is our (MQ and DS) standard of care for all NVG patients presenting with partially or completely open angles.</p><p><strong>Case: </strong>A 66-year-old man's right eye had a visual acuity of 20/50, intraocular pressure (IOP) of 42 mmHg on 0 IOP-lowering medications, and neovascularization of the iris and angle with no peripheral anterior synechiae. Fundoscopy revealed midperipheral dot-blot hemorrhages without diabetic retinopathy or vein occlusion. Fluorescein angiography revealed peripheral retinal nonperfusion in both eyes. The patient was diagnosed with open-angle NVG secondary to OIS and treated with 6 serial monthly anti-VEGF injections interspersed with 4 PRP sessions, after which his anterior segment neovascularization regressed and IOP normalized on 0 medications. Ten weeks after the last injection, the anterior segment neovascularization and elevated IOP recurred, so he underwent 4 more monthly anti-VEGF injections and 4 PRP sessions, after which his anterior segment neovascularization regressed and his IOP normalized on 0 medications. However, 6 weeks after the last injection, the anterior segment neovascularization and elevated IOP again recurred, so he was resumed on a third course of lifetime monthly anti-VEGF injections, which may be continued in perpetuity.</p><p><strong>Conclusion: </strong>The patient's NVG was quiescent while under the protection of serial anti-VEGF injections with interspersed PRP; however, the disease recurred each time injections were stopped. Therefore, in patients with open-angle NVG secondary to OIS, serial monthly anti-VEGF injections may be necessary combined with PRP to suppress underlying neovascular drive and regress anterior segment neovascularization, maintain physiologic IOP, and prevent synechial angle closure.</p>","PeriodicalId":9603,"journal":{"name":"Case Reports in Ophthalmological Medicine","volume":" ","pages":"4959522"},"PeriodicalIF":0.9,"publicationDate":"2022-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352498/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40592070","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: 2
Decentered Individualized Sphero-Cylindrical (DISC) Ablation and Corneal Crosslinking in Patient with Progressive Keratoconus. 进行性圆锥角膜患者的去中心个体化球-柱(DISC)消融和角膜交联。
IF 0.9
Case Reports in Ophthalmological Medicine Pub Date : 2022-07-21 eCollection Date: 2022-01-01 DOI: 10.1155/2022/1839848
Igor Knezović, Sara Djurić
{"title":"Decentered Individualized Sphero-Cylindrical (DISC) Ablation and Corneal Crosslinking in Patient with Progressive Keratoconus.","authors":"Igor Knezović,&nbsp;Sara Djurić","doi":"10.1155/2022/1839848","DOIUrl":"https://doi.org/10.1155/2022/1839848","url":null,"abstract":"<p><strong>Aim: </strong>To report a new method with which we have treated a 29-year-old patient with keratoconus and progressive bilateral visual loss during the past few years.</p><p><strong>Methods: </strong>The patient underwent inferotemporal decentered individualized sphero-cylindrical (DISC) ablation and crosslinking (CXL) of the left eye. After administration of topical anesthetic, the patient was subjected to phototherapeutic keratectomy (PTK) laser ablation of the central 7.0 mm optical zone with 50 <i>μ</i>m depth of epithelial ablation. To avoid the possible outcome of corneal haze, 0.02% mitomycin C (MMC) was applied to the stromal surface for 40 seconds. Riboflavin 0.1% solution was then administered topically every 2 minutes for a 30-minute period followed by 5 cycles of corneal crosslinking, radiating with UV-A at 3 mW/cm<sup>2</sup>, for a duration of 5 minutes.</p><p><strong>Results: </strong>17 months postoperative, there was an impressive improvement in uncorrected distance visual acuity, and the cornea became more regular. Results of Fourier's analysis imply a drop of irregularity (-28.6% two months and -63% seventeen months postoperative), Zernike analysis revealed a decrease of higher order aberrations (spheric and comatic aberrations), and corneal index values in the 8 mm zone (IHD, ISV, and IVA) became lower, compared to the preoperative values.</p><p><strong>Conclusion: </strong>It is possible to obtain better outcome of visual function with DISC ablation through an individual approach compared to CXL solely. This approach might be a promising strategy in retrieving impaired vision in patients suffering from keratoconus.</p>","PeriodicalId":9603,"journal":{"name":"Case Reports in Ophthalmological Medicine","volume":" ","pages":"1839848"},"PeriodicalIF":0.9,"publicationDate":"2022-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334114/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40660805","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
Novel Mutations in the MKKS, BBS7, and ALMS1 Genes in Iranian Children with Clinically Suspected Bardet-Biedl Syndrome. 伊朗临床疑似Bardet-Biedl综合征患儿中MKKS、BBS7和ALMS1基因的新突变
IF 0.9
Case Reports in Ophthalmological Medicine Pub Date : 2022-07-21 eCollection Date: 2022-01-01 DOI: 10.1155/2022/6110775
Roghayeh Dehghan, Mahdiyeh Behnam, Mansoor Salehi, Roya Kelishadi
{"title":"Novel Mutations in the <i>MKKS</i>, <i>BBS7</i>, and <i>ALMS1</i> Genes in Iranian Children with Clinically Suspected Bardet-Biedl Syndrome.","authors":"Roghayeh Dehghan,&nbsp;Mahdiyeh Behnam,&nbsp;Mansoor Salehi,&nbsp;Roya Kelishadi","doi":"10.1155/2022/6110775","DOIUrl":"https://doi.org/10.1155/2022/6110775","url":null,"abstract":"<p><p>Bardet-Biedl syndrome is a rare autosomal recessive form of syndromic obesity which is characterized by retinal degeneration, obesity, polydactyly, cognitive impairment, and renal and urogenital anomalies. In this study, we used whole-exome sequencing (WES) to investigate the underlying mutations in four Iranian children from consanguineous families with a clinical diagnosis of Bardet-Biedl syndrome (BBS). In three out of four children, we identified one previously reported frameshifting variant in the <i>BBS12</i> gene (c.265-266delTT, p.L89fs) and two novel nonsense variants in <i>MKKS</i> (c.1196T>G, p.L399X) and <i>BBS7</i> genes (c.1636C>T, p.Q546X). In the other child, no mutations were detected in known genes for BBS. However, we identified a novel variant in the <i>ALMS1</i> gene (c.10996delC, p.Q3666fs) indicative of Alström syndrome. All variants were interpreted as pathogenic according to American College of Medical Genetics and Genomics (ACMG) guidelines and confirmed through Sanger sequencing. In conclusion, our results not only expand the spectrum of mutations in BBS and <i>ALMS1</i> genes but also accentuate the importance of genetic testing for differentiating BBS from Alström syndrome.</p>","PeriodicalId":9603,"journal":{"name":"Case Reports in Ophthalmological Medicine","volume":" ","pages":"6110775"},"PeriodicalIF":0.9,"publicationDate":"2022-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334124/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40660806","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: 3
Intravitreal Brolucizumab for Choroidal Neovascularization Associated to Angioid Streaks. 玻璃体内Brolucizumab治疗血管样条纹相关脉络膜新生血管。
IF 0.9
Case Reports in Ophthalmological Medicine Pub Date : 2022-07-14 eCollection Date: 2022-01-01 DOI: 10.1155/2022/3442306
Somnath Chakraborty, Jay Umed Sheth
{"title":"Intravitreal Brolucizumab for Choroidal Neovascularization Associated to Angioid Streaks.","authors":"Somnath Chakraborty,&nbsp;Jay Umed Sheth","doi":"10.1155/2022/3442306","DOIUrl":"https://doi.org/10.1155/2022/3442306","url":null,"abstract":"<p><p>A 44-year-old-female with angioid streak- (AS-) associated choroidal-neovascularization (CNV) was treated with one dose of intravitreal brolucizumab (IB). At one-month, the patient's visual acuity (VA) improved from 20/120 to 20/40 with a dry macula on spectral-domain optical-coherence tomography (SD-OCT). After observation, the VA improved further to 20/32 with absence of any fluid on the SD-OCT at three months. No ocular or systemic adverse events were noted. In conclusion, intravitreal brolucizumab (IB) is an efficacious and safe therapeutic option for the management of CNV secondary to AS. Further prospective studies with a larger sample size, varied therapeutic regimens, and longer follow-up period are needed to corroborate our findings.</p>","PeriodicalId":9603,"journal":{"name":"Case Reports in Ophthalmological Medicine","volume":" ","pages":"3442306"},"PeriodicalIF":0.9,"publicationDate":"2022-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303153/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40536107","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
Iris Ring Melanoma Presenting as Scleral Pigmentation. 虹膜环黑色素瘤表现为巩膜色素沉着。
IF 0.9
Case Reports in Ophthalmological Medicine Pub Date : 2022-07-04 eCollection Date: 2022-01-01 DOI: 10.1155/2022/4840380
Matej Zupan, Alenka Lavrič, Jože Pižem, Katrina Novak Andrejčič
{"title":"Iris Ring Melanoma Presenting as Scleral Pigmentation.","authors":"Matej Zupan,&nbsp;Alenka Lavrič,&nbsp;Jože Pižem,&nbsp;Katrina Novak Andrejčič","doi":"10.1155/2022/4840380","DOIUrl":"https://doi.org/10.1155/2022/4840380","url":null,"abstract":"<p><p>To report a patient with a very rare variant of iris melanoma that grows in the shape of a ring (ring melanoma). A 65-year-old patient was examined because of a pigmented lesion on the sclera. After a complete ophthalmic and ultrasound examination, a ring melanoma was diagnosed. Enucleation of the affected eye was performed, and histology report confirmed iris ring melanoma. This type of malignancy represents an exceedingly rare variant of uveal melanoma, and because of atypical clinical picture, it can be easily overlooked or misdiagnosed, which often delays adequate treatment. Gonioscopy, transillumination, and ultrasound help us to recognize and diagnose ring melanoma. Suspicion should be raised with a clinical picture that shows unilateral pigmentary glaucoma. The objective of this presentation is to describe and outline the challenging diagnosis and management of this rare disease entity.</p>","PeriodicalId":9603,"journal":{"name":"Case Reports in Ophthalmological Medicine","volume":" ","pages":"4840380"},"PeriodicalIF":0.9,"publicationDate":"2022-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273431/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40503979","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: 1
Invasive Orbital Squamous Cell Carcinoma in a Patient with Multiple Myeloma. 侵袭性眼眶鳞状细胞癌合并多发性骨髓瘤1例。
IF 0.9
Case Reports in Ophthalmological Medicine Pub Date : 2022-06-29 eCollection Date: 2022-01-01 DOI: 10.1155/2022/8585692
Narges Karrabi, Kiana Hassanpour, Noushin Afshar Moghaddam, Faezeh Khorasanizadeh, Sadid Hooshmandi, Amirreza Veisi
{"title":"Invasive Orbital Squamous Cell Carcinoma in a Patient with Multiple Myeloma.","authors":"Narges Karrabi,&nbsp;Kiana Hassanpour,&nbsp;Noushin Afshar Moghaddam,&nbsp;Faezeh Khorasanizadeh,&nbsp;Sadid Hooshmandi,&nbsp;Amirreza Veisi","doi":"10.1155/2022/8585692","DOIUrl":"https://doi.org/10.1155/2022/8585692","url":null,"abstract":"<p><strong>Background: </strong>Orbital squamous cell carcinoma (SCC) is a rare entity. It is often a result of local invasion of SCC originating from the skin, nasopharynx, nasal cavity, paranasal sinuses, conjunctiva, lacrimal glands, or sac or less commonly occurs through hematogenous metastasis. Herein, we report a patient with orbital SCC with a history of multiple myeloma (MM). <i>Case presentation</i>. A 45-year-old woman with a history of MM in the past two years presented to our clinic complaining of gradual right eye proptosis for six months. The relative afferent pupillary defect was detected in the right eye on her examination. Ocular movements of the right eye were limited in all directions. Orbital magnetic resonance imaging demonstrated an infiltrative mass in the right orbit extended from the anterior to the orbital apex and the optic canal. The patient underwent debulking, and a histopathology examination revealed SCC results. No other secondary site was found to be the origin of the tumor.</p><p><strong>Result: </strong>The patient underwent chemotherapy and subsequent radiotherapy. To our knowledge, this is the first report of concomitant MM and primary orbital SCC.</p>","PeriodicalId":9603,"journal":{"name":"Case Reports in Ophthalmological Medicine","volume":" ","pages":"8585692"},"PeriodicalIF":0.9,"publicationDate":"2022-06-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9259366/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40580312","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: 4
Cystoid Macular Edema 18 Years after Anterior Chamber Phakic Intraocular Lens Implantation. 前房人工晶状体植入术后18年黄斑囊样水肿。
IF 0.9
Case Reports in Ophthalmological Medicine Pub Date : 2022-06-16 eCollection Date: 2022-01-01 DOI: 10.1155/2022/1853248
Elias L Warrak, Majd S Haddam, Walid N Dandan, John E Warrak, Fady K Sammouh
{"title":"Cystoid Macular Edema 18 Years after Anterior Chamber Phakic Intraocular Lens Implantation.","authors":"Elias L Warrak,&nbsp;Majd S Haddam,&nbsp;Walid N Dandan,&nbsp;John E Warrak,&nbsp;Fady K Sammouh","doi":"10.1155/2022/1853248","DOIUrl":"https://doi.org/10.1155/2022/1853248","url":null,"abstract":"<p><p>We report a case of a 54-year-old female patient who underwent PAC-IOL implantation 18 years prior to presentation. The patient had a best corrected visual acuity (BCVA) 20/20 in the right eye (OD) postoperatively with normal eye exam on routine follow-up since then. The patient presented for acute onset decreased visual acuity in the right eye. BCVA was 20/60, and exam showed blunted macular reflex with no evidence of inflammation. Optical coherence tomography (OCT) showed CME. She was started on topical treatment (ketorolac 0.5%) OD four times daily. Three weeks later, the patient had a BCVA of 20/20 OD with a normal macular reflex and an OCT showing the resolution of the CME. To our knowledge, this is the first reported case of a CME 18 years post PAC-IOL implantation. The possible cause of this incidence could be related to subclinical intraocular inflammation. Ophthalmologists should be aware of the possibility of such a latent CME post-PAC-IOL implantation.</p>","PeriodicalId":9603,"journal":{"name":"Case Reports in Ophthalmological Medicine","volume":" ","pages":"1853248"},"PeriodicalIF":0.9,"publicationDate":"2022-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225911/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40402572","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
Multimodal Imaging of Subfoveal Pachydrusen Containing a Blood Flow Signal. 含有血流信号的中央凹下脓肿的多模态成像。
IF 0.9
Case Reports in Ophthalmological Medicine Pub Date : 2022-06-08 eCollection Date: 2022-01-01 DOI: 10.1155/2022/5680913
Naoko Ishiguro, Takaaki Hayashi, Yoshiko Yamawaki, Kei Mizobuchi, Tsutomu Yasukawa, Shigeru Honda, Tadashi Nakano
{"title":"Multimodal Imaging of Subfoveal Pachydrusen Containing a Blood Flow Signal.","authors":"Naoko Ishiguro,&nbsp;Takaaki Hayashi,&nbsp;Yoshiko Yamawaki,&nbsp;Kei Mizobuchi,&nbsp;Tsutomu Yasukawa,&nbsp;Shigeru Honda,&nbsp;Tadashi Nakano","doi":"10.1155/2022/5680913","DOIUrl":"https://doi.org/10.1155/2022/5680913","url":null,"abstract":"<p><p>Individuals with pachydrusen, larger than 125 <i>μ</i>m, have a significantly thicker choroid than do those with soft drusen or reticular pseudodrusen. Little is known about cases of abnormal blood flow within pachydrusen. The purpose of this report was to demonstrate a blood flow signal within pachydrusen using optical coherence tomography (OCT) angiography. A 76-year-old Japanese woman presented with innumerable drusen/pachydrusen in both posterior poles. Her visual acuity was good. OCT showed subfoveal pachydrusen in the left eye, but no exudative changes. The subfoveal choroidal thickness was increased to 274 <i>μ</i>m in the left eye. OCT angiography revealed a blood flow signal within the pachydrusen. However, fluorescein and indocyanine green angiographies indicated no abnormal hyperfluorescent lesion in the macula of the left eye. During the 13-month follow-up, the blood flow signal in OCT angiography did not change in diameter, and no exudative change was observed. The blood flow signal may have properties of capillary blood vessels derived from the choriocapillaris, rather than angiogenic vessels from choroidal neovascularization or polypoidal choroidal vasculopathy/aneurysmal type 1 neovascularization.</p>","PeriodicalId":9603,"journal":{"name":"Case Reports in Ophthalmological Medicine","volume":" ","pages":"5680913"},"PeriodicalIF":0.9,"publicationDate":"2022-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200588/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40041098","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
Paracentral Acute Middle Maculopathy and Nonischemic Central Retinal Vein Obstruction in a Young Patient with Protein C Deficiency 一名年轻蛋白C缺乏患者的中央旁急性中黄斑病变和非缺血性视网膜中央静脉阻塞
IF 0.9
Case Reports in Ophthalmological Medicine Pub Date : 2022-06-06 DOI: 10.1155/2022/1237148
M. Abrishami, S. Hosseini, Nasser Shoeibi, Hamid-Reza Heidarzadeh
{"title":"Paracentral Acute Middle Maculopathy and Nonischemic Central Retinal Vein Obstruction in a Young Patient with Protein C Deficiency","authors":"M. Abrishami, S. Hosseini, Nasser Shoeibi, Hamid-Reza Heidarzadeh","doi":"10.1155/2022/1237148","DOIUrl":"https://doi.org/10.1155/2022/1237148","url":null,"abstract":"Purpose To report a case of protein C deficiency with paracentral acute middle maculopathy (PAMM) and nonischemic central retinal vein obstruction (NI-CRVO). Case Report. A previously healthy twenty-one-year-old male was referred with sudden-onset, painless, unilateral paracentral scotomata in the right eye for a week. His uncorrected visual acuity was 20/20 in both eyes. In fundus examination of the right eye, mild venous tortuosity, retinal hemorrhages, and a gray-white opacity in the papillomacular bundle were observed. In the macular spectral-domain optical coherence tomography images, a hyperreflective band was noticed at the level of the inner nuclear layer, indicating PAMM. Fundus appearance and fluorescein angiography findings indicated NI-CRVO diagnosis made. The systemic and laboratory evaluations disclosed a protein C deficiency. Conclusion In this report, in a healthy young male, combined PAMM and NI-CRVO showed to be the cause of blurred vision in the setting of protein C deficiency.","PeriodicalId":9603,"journal":{"name":"Case Reports in Ophthalmological Medicine","volume":"2 1","pages":""},"PeriodicalIF":0.9,"publicationDate":"2022-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83821993","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: 1
A New Mechanism of Silicone Oil-Induced Glaucoma and Its Management 硅油致青光眼的新机制及治疗
IF 0.9
Case Reports in Ophthalmological Medicine Pub Date : 2022-06-02 DOI: 10.1155/2022/2343139
H. Kumar, D. Talwar, Mithun Thulasidas, Surbi Taneja
{"title":"A New Mechanism of Silicone Oil-Induced Glaucoma and Its Management","authors":"H. Kumar, D. Talwar, Mithun Thulasidas, Surbi Taneja","doi":"10.1155/2022/2343139","DOIUrl":"https://doi.org/10.1155/2022/2343139","url":null,"abstract":"Purpose To describe a case of secondary acute angle closure glaucoma due to silicone oil migration into the posterior chamber causing entrapment of aqueous and its successful management. Case Presentation. A 69-year-old female presented with decreased vision and pain in the left eye (LE) for one month. She had a history of complicated phacoemulsification with nucleus drop and retinal detachment in LE, for which vitreoretinal surgery with silicone oil endotamponade was done. She was also a known case of primary open angle glaucoma on medications. The corrected distance visual acuity was 20/20 and 20/125 in the right eye (RE) and LE, respectively. The intraocular pressure (IOP) was 18 mmHg in RE and 45 mmHg in LE. Anterior segment examination of LE revealed 270° of iridocorneal apposition in the periphery of the anterior chamber. Fundus examination of LE showed silicone oil filled vitreous cavity with attached retina. Given the recent history of silicone oil injection and elevated IOP despite maximum antiglaucoma medications, we decided to perform laser peripheral iridotomy (LPI) in the area of iridocorneal apposition. Following LPI, the IOP in LE came down to 17 mmHg and remained stable within the normal range for one month, after which the patient was taken up for silicone oil removal. Conclusion This case report highlights a new mechanism of silicone oil-induced glaucoma and the technique of performing LPI in the area of iridocorneal apposition, for the first time in the literature. Silicone oil migration into the posterior chamber from the vitreous cavity in the presence of zonular dehiscence can push the iris forward and lead to iridocorneal apposition, resulting in an acute rise in IOP. Performing LPI within the area of iridocorneal apposition can help the aqueous seep into the anterior chamber and release the silicone oil globule trapped behind the iris to enter the anterior chamber, thus relieving the iridocorneal adhesions and lowering the IOP.","PeriodicalId":9603,"journal":{"name":"Case Reports in Ophthalmological Medicine","volume":"14 1","pages":""},"PeriodicalIF":0.9,"publicationDate":"2022-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74839953","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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