Abstract
Purpose
To report a case of melanoma-associated retinopathy (MAR) with autoantibodies against the transient receptor potential cation channel, subfamily M, member 1 (TRPM1) with asymmetric severe vision loss.
Methods
We evaluated a patient with heel skin melanoma showing progressive vision loss in both eyes confirmed with a baseline ophthalmic examination, fluorescein angiography, spectral domain optical coherence tomography (OCT), visual field test, and full-field electroretinogram (ERG). Immunofluorescence assays and western blot analysis revealed autoantibodies in the patient’s serum.
Results
The patient’s best-corrected visual acuities were 20/50 in the right eye and hand motion in the left eye. Visual field test showed severely depressed visual fields especially in the left eye. Fluorescein angiography and OCT revealed extrafoveal choroidal neovascularization in the left eye. The patient had an electronegative ERG, suggesting MAR, and autoantibodies against TRPM1 and aldolase C were detected in the patient’s blood sample.
Conclusions
The clinical features of MAR patients with positive anti-TRPM1 autoantibodies can be manifested as severe vision loss, and the identification of autoantibodies can be helpful for confirming the diagnosis.
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Acknowledgements
This study was supported by Grant No. 14-2018-019 from the SNUBH Research Fund.
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Kim, M.S., Hong, H.K., Ko, Y.J. et al. A case of melanoma-associated retinopathy with autoantibodies against TRPM1. Doc Ophthalmol 141, 313–318 (2020). https://doi.org/10.1007/s10633-020-09772-1
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DOI: https://doi.org/10.1007/s10633-020-09772-1