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Autoimmune retinopathy and optic neuropathy associated with enolase-positive renal oncocytoma

PURPOSE: To report a case of autoimmune retinopathy and optic neuropathy associated with an enolase-positive renal oncocytoma. OBSERVATIONS: A 41-year-old man presented with subacute, painless, bilateral vision loss. On initial examination, visual acuity measured 20/125 OD and 20/1250 OS, and telang...

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Autores principales: Cheng, Justine L., Beebe, Johanna D., Nepple, Kenneth G., Zakharia, Yousef, Mullins, Robert F., Flamme-Wiese, Miles J., Thurtell, Matthew J., Han, Ian C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6140802/
https://www.ncbi.nlm.nih.gov/pubmed/30229140
http://dx.doi.org/10.1016/j.ajoc.2018.09.005
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author Cheng, Justine L.
Beebe, Johanna D.
Nepple, Kenneth G.
Zakharia, Yousef
Mullins, Robert F.
Flamme-Wiese, Miles J.
Thurtell, Matthew J.
Han, Ian C.
author_facet Cheng, Justine L.
Beebe, Johanna D.
Nepple, Kenneth G.
Zakharia, Yousef
Mullins, Robert F.
Flamme-Wiese, Miles J.
Thurtell, Matthew J.
Han, Ian C.
author_sort Cheng, Justine L.
collection PubMed
description PURPOSE: To report a case of autoimmune retinopathy and optic neuropathy associated with an enolase-positive renal oncocytoma. OBSERVATIONS: A 41-year-old man presented with subacute, painless, bilateral vision loss. On initial examination, visual acuity measured 20/125 OD and 20/1250 OS, and telangiectatic vessels were noted on the optic nerves and in the maculae. Goldmann perimetry showed bilateral, cecocentral scotomas, and electroretinography demonstrated reduced photopic and scotopic signals, concerning for autoimmune retinopathy. Serum testing showed multiple positive anti-optic nerve and anti-retinal antibodies, including to alpha-enolase. Extensive systemic workup was negative except for a large, exophytic, right renal mass. Biopsy was consistent with a benign oncocytoma, and immunohistochemical staining showed diffusely positive alpha-enolase staining. The patient was treated with a five-day course of intravenous methylprednisolone and plasmapheresis with minimal improvement. Surgical excision of the oncocytoma was performed. At 9-months post-operatively, visual acuity had improved to 20/40 OU, with corresponding improvement on visual field and electroretinography testing. CONCLUSIONS AND IMPORTANCE: To our knowledge, this is the first report of autoimmune retinopathy and optic neuropathy associated with a renal oncocytoma. The case highlights the importance of a thorough systemic workup in cases of suspected autoimmune retinopathy and reminds clinicians that even tumors considered benign can have distal effects on other organs.
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spelling pubmed-61408022018-09-18 Autoimmune retinopathy and optic neuropathy associated with enolase-positive renal oncocytoma Cheng, Justine L. Beebe, Johanna D. Nepple, Kenneth G. Zakharia, Yousef Mullins, Robert F. Flamme-Wiese, Miles J. Thurtell, Matthew J. Han, Ian C. Am J Ophthalmol Case Rep Case report PURPOSE: To report a case of autoimmune retinopathy and optic neuropathy associated with an enolase-positive renal oncocytoma. OBSERVATIONS: A 41-year-old man presented with subacute, painless, bilateral vision loss. On initial examination, visual acuity measured 20/125 OD and 20/1250 OS, and telangiectatic vessels were noted on the optic nerves and in the maculae. Goldmann perimetry showed bilateral, cecocentral scotomas, and electroretinography demonstrated reduced photopic and scotopic signals, concerning for autoimmune retinopathy. Serum testing showed multiple positive anti-optic nerve and anti-retinal antibodies, including to alpha-enolase. Extensive systemic workup was negative except for a large, exophytic, right renal mass. Biopsy was consistent with a benign oncocytoma, and immunohistochemical staining showed diffusely positive alpha-enolase staining. The patient was treated with a five-day course of intravenous methylprednisolone and plasmapheresis with minimal improvement. Surgical excision of the oncocytoma was performed. At 9-months post-operatively, visual acuity had improved to 20/40 OU, with corresponding improvement on visual field and electroretinography testing. CONCLUSIONS AND IMPORTANCE: To our knowledge, this is the first report of autoimmune retinopathy and optic neuropathy associated with a renal oncocytoma. The case highlights the importance of a thorough systemic workup in cases of suspected autoimmune retinopathy and reminds clinicians that even tumors considered benign can have distal effects on other organs. Elsevier 2018-09-10 /pmc/articles/PMC6140802/ /pubmed/30229140 http://dx.doi.org/10.1016/j.ajoc.2018.09.005 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case report
Cheng, Justine L.
Beebe, Johanna D.
Nepple, Kenneth G.
Zakharia, Yousef
Mullins, Robert F.
Flamme-Wiese, Miles J.
Thurtell, Matthew J.
Han, Ian C.
Autoimmune retinopathy and optic neuropathy associated with enolase-positive renal oncocytoma
title Autoimmune retinopathy and optic neuropathy associated with enolase-positive renal oncocytoma
title_full Autoimmune retinopathy and optic neuropathy associated with enolase-positive renal oncocytoma
title_fullStr Autoimmune retinopathy and optic neuropathy associated with enolase-positive renal oncocytoma
title_full_unstemmed Autoimmune retinopathy and optic neuropathy associated with enolase-positive renal oncocytoma
title_short Autoimmune retinopathy and optic neuropathy associated with enolase-positive renal oncocytoma
title_sort autoimmune retinopathy and optic neuropathy associated with enolase-positive renal oncocytoma
topic Case report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6140802/
https://www.ncbi.nlm.nih.gov/pubmed/30229140
http://dx.doi.org/10.1016/j.ajoc.2018.09.005
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