Nicolas Nicolaou, Despina Nicolaou, Constantinos Nicolaou
{"title":"无痛性非进展性多灶脉络膜病变:基于相似性的文献回顾与病例报告。","authors":"Nicolas Nicolaou, Despina Nicolaou, Constantinos Nicolaou","doi":"10.1080/09273948.2024.2435471","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To present a case of indolent, nonprogressive multifocal choroidal lesions and contribute to the limited reports aiding this diagnosis, supplemented by a review of the literature.</p><p><strong>Methods: </strong>Clinical records of a patient were reviewed alongside relevant literature from PubMed, Cochrane, and Google Scholar.</p><p><strong>Results: </strong>A male in late 50s presented with a 10-year history of unilateral yellow-white asymptomatic fundus lesions in the left eye. Extensive multimodal imaging and workup for systemic lymphoma, sarcoidosis, autoimmune diseases, birdshot chorioretinopathy, and related infections yielded negative results. Indocyanine Green Angiography (ICGA) revealed hypofluorescent spots in the mid-late frames and fluorescence blockage consistent with fundus lesions. Enhanced-depth OCT revealed choroidal thickening and hyporeflective spaces within the outer choroid corresponding to the lesions. During Fluorescein angiography, the lesions became more iso-fluorescent and stained minimally in the late phase, indicating they are not full thickness and spare the inner choroid. Short-wave autofluorescence was normal. B-scan ultrasound revealed two shallow, lesions without retinal infiltration. Partial lesion regression and progression were observed over time. Steroid treatment aimed at reducing lesion choroidal thickening had a mild effect. Despite discontinuation, the patient remained asymptomatic without vision impairment or intraocular inflammation. The right eye remained unaffected.</p><p><strong>Conclusion: </strong>Indolent, nonprogressive, multifocal, and choroidal lesions likely represent benign lymphocytic infiltrates localised within the outer choroid. Mild steroid response suggests a non-inflammatory process. The lack of reports presents a gap in ophthalmology. Diagnosis of this case is based on similar presentation of other cases. Surveillance rather than biopsy or treatment is recommended for asymptomatic patients.</p>","PeriodicalId":19406,"journal":{"name":"Ocular Immunology and Inflammation","volume":" ","pages":"1-5"},"PeriodicalIF":2.6000,"publicationDate":"2024-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Indolent Nonprogressive Multifocal Choroidal Lesions: A Review of Literature and Case Report Based on Similarity.\",\"authors\":\"Nicolas Nicolaou, Despina Nicolaou, Constantinos Nicolaou\",\"doi\":\"10.1080/09273948.2024.2435471\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>To present a case of indolent, nonprogressive multifocal choroidal lesions and contribute to the limited reports aiding this diagnosis, supplemented by a review of the literature.</p><p><strong>Methods: </strong>Clinical records of a patient were reviewed alongside relevant literature from PubMed, Cochrane, and Google Scholar.</p><p><strong>Results: </strong>A male in late 50s presented with a 10-year history of unilateral yellow-white asymptomatic fundus lesions in the left eye. Extensive multimodal imaging and workup for systemic lymphoma, sarcoidosis, autoimmune diseases, birdshot chorioretinopathy, and related infections yielded negative results. Indocyanine Green Angiography (ICGA) revealed hypofluorescent spots in the mid-late frames and fluorescence blockage consistent with fundus lesions. Enhanced-depth OCT revealed choroidal thickening and hyporeflective spaces within the outer choroid corresponding to the lesions. During Fluorescein angiography, the lesions became more iso-fluorescent and stained minimally in the late phase, indicating they are not full thickness and spare the inner choroid. Short-wave autofluorescence was normal. B-scan ultrasound revealed two shallow, lesions without retinal infiltration. Partial lesion regression and progression were observed over time. Steroid treatment aimed at reducing lesion choroidal thickening had a mild effect. Despite discontinuation, the patient remained asymptomatic without vision impairment or intraocular inflammation. The right eye remained unaffected.</p><p><strong>Conclusion: </strong>Indolent, nonprogressive, multifocal, and choroidal lesions likely represent benign lymphocytic infiltrates localised within the outer choroid. Mild steroid response suggests a non-inflammatory process. The lack of reports presents a gap in ophthalmology. Diagnosis of this case is based on similar presentation of other cases. Surveillance rather than biopsy or treatment is recommended for asymptomatic patients.</p>\",\"PeriodicalId\":19406,\"journal\":{\"name\":\"Ocular Immunology and Inflammation\",\"volume\":\" \",\"pages\":\"1-5\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2024-12-06\",\"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/10.1080/09273948.2024.2435471\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"OPHTHALMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ocular Immunology and Inflammation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/09273948.2024.2435471","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
Indolent Nonprogressive Multifocal Choroidal Lesions: A Review of Literature and Case Report Based on Similarity.
Purpose: To present a case of indolent, nonprogressive multifocal choroidal lesions and contribute to the limited reports aiding this diagnosis, supplemented by a review of the literature.
Methods: Clinical records of a patient were reviewed alongside relevant literature from PubMed, Cochrane, and Google Scholar.
Results: A male in late 50s presented with a 10-year history of unilateral yellow-white asymptomatic fundus lesions in the left eye. Extensive multimodal imaging and workup for systemic lymphoma, sarcoidosis, autoimmune diseases, birdshot chorioretinopathy, and related infections yielded negative results. Indocyanine Green Angiography (ICGA) revealed hypofluorescent spots in the mid-late frames and fluorescence blockage consistent with fundus lesions. Enhanced-depth OCT revealed choroidal thickening and hyporeflective spaces within the outer choroid corresponding to the lesions. During Fluorescein angiography, the lesions became more iso-fluorescent and stained minimally in the late phase, indicating they are not full thickness and spare the inner choroid. Short-wave autofluorescence was normal. B-scan ultrasound revealed two shallow, lesions without retinal infiltration. Partial lesion regression and progression were observed over time. Steroid treatment aimed at reducing lesion choroidal thickening had a mild effect. Despite discontinuation, the patient remained asymptomatic without vision impairment or intraocular inflammation. The right eye remained unaffected.
Conclusion: Indolent, nonprogressive, multifocal, and choroidal lesions likely represent benign lymphocytic infiltrates localised within the outer choroid. Mild steroid response suggests a non-inflammatory process. The lack of reports presents a gap in ophthalmology. Diagnosis of this case is based on similar presentation of other cases. Surveillance rather than biopsy or treatment is recommended for asymptomatic patients.
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.