TO THE EDITOR:
I commend Hearne et al on their effort to raise awareness of vitreoretinal lymphoma (VRL) [1]. However, I respectfully disagree with the authors’ interpretation of the term ‘primary’, which implies that the disease originates intraocularly. This may not be the case, even if systemic investigations are negative. I had a patient with VRL with sheathing and occlusion of the inferotemporal retinal arterioles in the left eye; she subsequently developed lymphomatous deposits throughout the fundus, except in the area of the vascular occlusion. This case suggests a systemic source of the lymphoma cells, which percolate through the retinal pigment epithelium to accumulate at Bruch’s membrane [2].
At the University of California, San Francisco, we hypothesised that if VRL is a systemic disease, then systemic treatment is more likely to prolong life than ocular treatment, which we considered to be only symptomatic or palliative. We achieved encouraging ocular and systemic outcomes by treating VRL with systemic chemotherapy, which (importantly) was followed by long-term maintenance immunotherapy to suppress any minimal residual disease [3]. Vitreous infiltrates were more resistant to systemic treatment, whose efficacy increased following therapeutic vitrectomy [4].
Hearne et al. use the term ‘primary intraocular lymphoma (PIOL)’ synonymously with VRL; however, PIOL includes uveal lymphoma, which is quite different, consisting of low-grade extranodal marginal-zone lymphoma, with an excellent survival probability. PIOL is therefore an umbrella term and should be recognised as such.
Hearne et al. cite an article on metagenomic deep sequencing by Gonzales et al. but missed the opportunity to emphasise the great diagnostic potential of this test, which detects MYD88 mutation, a well-recognised lymphoma biomarker, and which also identifies the organisms causing any infectious uveitis or, indeed, lymphoma [5].
I have seen several patients whose VRL diagnosis was delayed by many months of futile uveitis therapy so that any opportunities for conserving vision and life were missed. These tragic outcomes could be avoided if more ophthalmologists learn to recognise the VRL signs on fundus autofluorescence imaging and optical coherence tomography and if they send these images to an ocular oncologist for a second opinion at the slightest suspicion of this highly lethal disease.
References
Hearne E, Netzer OT, Lightman S. Learning points in intraocular lymphoma. Eye. 2021;35:1815–7.
Damato BE, Bever GJ, Afshar AR, Rubenstein JL. Insights from a Case of Vitreoretinal Lymphoma. Ocul Oncol Pathol. 2019;5:13–9.
Damato B, Bever GJ, Kim DJ, Afshar AR, Rubenstein JL. An audit of retinal lymphoma treatment at the University of California San Francisco. Eye. 2020;34:515–22.
Bever GJ, Kim DJ, Afshar AR, Rubenstein JL, Damato BE. Therapeutic vitrectomy as an adjunct treatment to systemic chemotherapy for intraocular lymphoma. Retin Cases Brief Rep. 2020;14:116–9.
Gonzales J, Doan T, Shantha JG, Bloomer M, Wilson MR, DeRisi JL, et al. Metagenomic deep sequencing of aqueous fluid detects intraocular lymphomas. Br J Ophthalmol. 2018;102:6–8.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Competing interests
The author declares no competing interests.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Damato, B. Vitreoretinal lymphoma: an alternative view. Eye 36, 1845 (2022). https://doi.org/10.1038/s41433-021-01841-2
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1038/s41433-021-01841-2