Spontaneous Regression of Vitreoretinal Lymphoma Lesions: Case Series and Literature Review.

IF 1.7 4区 医学 Q2 OPHTHALMOLOGY
Federico Rissotto, Stefano Lingardo, Gloria Oldoni, Francesco Bandello, Maria Vittoria Cicinelli, Elisabetta Miserocchi
{"title":"Spontaneous Regression of Vitreoretinal Lymphoma Lesions: Case Series and Literature Review.","authors":"Federico Rissotto, Stefano Lingardo, Gloria Oldoni, Francesco Bandello, Maria Vittoria Cicinelli, Elisabetta Miserocchi","doi":"10.1080/09273948.2026.2734578","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To describe a case series of spontaneous regression of vitreoretinal lymphoma (VRL) lesions documented through multimodal imaging and to contextualize findings with a review of the literature.</p><p><strong>Methods: </strong>We report five Caucasian patients with biopsy-confirmed VRL. All patients underwent multimodal imaging, including spectral-domain optical coherence tomography (SD-OCT), ultra-widefield (UWF) pseudocolor, and autofluorescence (AF) imaging, and fluorescein angiography (FA). Clinical and imaging data were reviewed to assess the occurrence of spontaneous lesion regression.</p><p><strong>Results: </strong>Spontaneous regression of VRL lesions was observed both in treatment-naïve patients and in patients under surveillance following prior systemic or intravitreal therapy. In one case, bilateral regression of optic nerve infiltration was observed; in two cases, unilateral regression of subretinal or sub-RPE lesions occurred; and in two cases, retinitis-like lesions spontaneously regressed.</p><p><strong>Conclusions: </strong>Spontaneous regression of VRL is a rare but clinically relevant phenomenon that may follow diagnostic interventions such as vitrectomy, possibly via immune-mediated mechanisms. Multimodal imaging is essential for documenting regression and guiding clinical management. Awareness of this phenomenon may prevent misinterpretation of disease activity and inform the need for close follow-up, even when apparent lesion regression occurs.</p>","PeriodicalId":19406,"journal":{"name":"Ocular Immunology and Inflammation","volume":" ","pages":"1-9"},"PeriodicalIF":1.7000,"publicationDate":"2026-09-22","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/10.1080/09273948.2026.2734578","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 describe a case series of spontaneous regression of vitreoretinal lymphoma (VRL) lesions documented through multimodal imaging and to contextualize findings with a review of the literature.

Methods: We report five Caucasian patients with biopsy-confirmed VRL. All patients underwent multimodal imaging, including spectral-domain optical coherence tomography (SD-OCT), ultra-widefield (UWF) pseudocolor, and autofluorescence (AF) imaging, and fluorescein angiography (FA). Clinical and imaging data were reviewed to assess the occurrence of spontaneous lesion regression.

Results: Spontaneous regression of VRL lesions was observed both in treatment-naïve patients and in patients under surveillance following prior systemic or intravitreal therapy. In one case, bilateral regression of optic nerve infiltration was observed; in two cases, unilateral regression of subretinal or sub-RPE lesions occurred; and in two cases, retinitis-like lesions spontaneously regressed.

Conclusions: Spontaneous regression of VRL is a rare but clinically relevant phenomenon that may follow diagnostic interventions such as vitrectomy, possibly via immune-mediated mechanisms. Multimodal imaging is essential for documenting regression and guiding clinical management. Awareness of this phenomenon may prevent misinterpretation of disease activity and inform the need for close follow-up, even when apparent lesion regression occurs.

玻璃体视网膜淋巴瘤病变的自发消退:病例系列和文献回顾。
目的:描述一系列通过多模态成像记录的玻璃体视网膜淋巴瘤(VRL)病变自发消退的病例,并通过文献综述将结果联系起来。方法:我们报告了5例活检证实的白种人VRL。所有患者都接受了多模态成像,包括光谱域光学相干断层扫描(SD-OCT)、超宽视场(UWF)假色、自体荧光(AF)成像和荧光素血管造影(FA)。回顾临床和影像学资料,以评估自发性病变消退的发生。结果:在treatment-naïve患者和在既往全身或玻璃体内治疗后接受监测的患者中,均观察到VRL病变自发消退。1例视神经浸润双侧退行;2例视网膜下或rpe下病变单侧消退;在两个病例中,视网膜样病变自发消退。结论:VRL的自发消退是一种罕见但与临床相关的现象,可能在玻璃体切除术等诊断干预措施之后,可能通过免疫介导的机制。多模态成像对于记录退化和指导临床治疗是必不可少的。认识到这一现象可以防止对疾病活动的误解,并告知需要密切随访,即使出现明显的病变消退。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
6.20
自引率
15.20%
发文量
285
审稿时长
6-12 weeks
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书