Alexandre Barbé, Sarah Mrejen, Diana Bratu, Francesc March de Ribot, Nathalie Massamba, Christine Fardeau, Bahram Bodaghi, Sara Touhami
{"title":"Torpedo Maculopathy Complicated by Macular Neovascularization and Secondary Multiple Evanescent White Dot Syndrome.","authors":"Alexandre Barbé, Sarah Mrejen, Diana Bratu, Francesc March de Ribot, Nathalie Massamba, Christine Fardeau, Bahram Bodaghi, Sara Touhami","doi":"10.1080/09273948.2026.2736172","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To report a case of torpedo maculopathy complicated by choroidal neovascularization (CNV) followed by secondary multiple evanescent white dot syndrome (MEWDS).</p><p><strong>Methods: </strong>Case report.</p><p><strong>Results: </strong>A 28-year-old male was referred for acute vision loss in his right eye. Fundus examination revealed a torpedo-shaped lesion temporal to the fovea. Optical coherence tomography (OCT) revealed a pigment epithelium detachment (PED) with overlying subretinal hyper-reflective material (SHRM), flow signal on OCT-angiography as well as hyper fluorescence on fluorescein angiography, consistent with CNV. More peripheral to the macula, indocyanine green angiography revealed multiple late-phase hypo fluorescent spots being hyper-autofluorescent on fundus autofluorescence and exhibiting ellipsoid zone disruption on OCT, supporting the diagnosis of secondary MEWDS.</p><p><strong>Conclusion: </strong>This is the first reported case of torpedo maculopathy complicated by both CNV and MEWDS. This case study exemplifies how congenital macular anomalies can progress to neovascular and inflammatory complications.</p>","PeriodicalId":19406,"journal":{"name":"Ocular Immunology and Inflammation","volume":" ","pages":"1-4"},"PeriodicalIF":1.7000,"publicationDate":"2026-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ocular Immunology and Inflammation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/09273948.2026.2736172","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: To report a case of torpedo maculopathy complicated by choroidal neovascularization (CNV) followed by secondary multiple evanescent white dot syndrome (MEWDS).
Methods: Case report.
Results: A 28-year-old male was referred for acute vision loss in his right eye. Fundus examination revealed a torpedo-shaped lesion temporal to the fovea. Optical coherence tomography (OCT) revealed a pigment epithelium detachment (PED) with overlying subretinal hyper-reflective material (SHRM), flow signal on OCT-angiography as well as hyper fluorescence on fluorescein angiography, consistent with CNV. More peripheral to the macula, indocyanine green angiography revealed multiple late-phase hypo fluorescent spots being hyper-autofluorescent on fundus autofluorescence and exhibiting ellipsoid zone disruption on OCT, supporting the diagnosis of secondary MEWDS.
Conclusion: This is the first reported case of torpedo maculopathy complicated by both CNV and MEWDS. This case study exemplifies how congenital macular anomalies can progress to neovascular and inflammatory complications.
期刊介绍:
Ocular Immunology & Inflammation ranks 18 out of 59 in the Ophthalmology Category.Ocular Immunology and Inflammation is a peer-reviewed, scientific publication that welcomes the submission of original, previously unpublished manuscripts directed to ophthalmologists and vision scientists. Published bimonthly, the journal provides an international medium for basic and clinical research reports on the ocular inflammatory response and its control by the immune system. The journal publishes original research papers, case reports, reviews, letters to the editor, meeting abstracts, and invited editorials.