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Optic Neuropathy Secondary to Polyarteritis Nodosa, Case Report, and Diagnostic Challenges

PURPOSE: To describe a case of optic neuropathy as a primary manifestation of polyarteritis nodosa (PAN) and discuss diagnostic challenges. METHODS: Case report. RESULTS: A 41-year-old Hispanic man presented with a 2-day history of reduced visual acuity in his left eye. Physical examination revealed...

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Autores principales: Vazquez-Romo, Kristian A., Rodriguez-Hernandez, Adrian, Paczka, Jose A., Nuño-Suarez, Moises A., Rocha-Muñoz, Alberto D., Zavala-Cerna, Maria G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611380/
https://www.ncbi.nlm.nih.gov/pubmed/28979236
http://dx.doi.org/10.3389/fneur.2017.00490
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author Vazquez-Romo, Kristian A.
Rodriguez-Hernandez, Adrian
Paczka, Jose A.
Nuño-Suarez, Moises A.
Rocha-Muñoz, Alberto D.
Zavala-Cerna, Maria G.
author_facet Vazquez-Romo, Kristian A.
Rodriguez-Hernandez, Adrian
Paczka, Jose A.
Nuño-Suarez, Moises A.
Rocha-Muñoz, Alberto D.
Zavala-Cerna, Maria G.
author_sort Vazquez-Romo, Kristian A.
collection PubMed
description PURPOSE: To describe a case of optic neuropathy as a primary manifestation of polyarteritis nodosa (PAN) and discuss diagnostic challenges. METHODS: Case report. RESULTS: A 41-year-old Hispanic man presented with a 2-day history of reduced visual acuity in his left eye. Physical examination revealed a complete visual field loss in the affected eye. Best-corrected visual acuity (BCVA) in the left eye was hand motion, and fundus examination revealed a hyperemic optic disk with blurred margins, swelling, retinal folds, dilated veins, and normal size arteries. BCVA in the right eye was 20/20; no anomalies were seen during examination of the fundus. The patient was started on oral corticosteroids and once the diagnosis of PAN was made, cyclophosphamide was added to the treatment regimen. Six months later, the patient recovered his BCVA to 20/20 in his left eye. CONCLUSION: Rarely does optic neuropathy present as a primary manifestation of PAN; nevertheless, it represents an ophthalmologic emergency that requires expeditious anti-inflammatory and immunosuppressive treatment to decrease the probability of permanent visual damage. Unfortunately, diagnosing PAN is challenging as it necessitates a high index of suspicion. In young male patients who present for the first time with diminished visual acuity, ophthalmologists become cornerstones in the suspicion of this diagnosis and should be responsible for continuing the study until a diagnosis is reached to ensure rapid commencement of immunosuppressive treatment.
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spelling pubmed-56113802017-10-04 Optic Neuropathy Secondary to Polyarteritis Nodosa, Case Report, and Diagnostic Challenges Vazquez-Romo, Kristian A. Rodriguez-Hernandez, Adrian Paczka, Jose A. Nuño-Suarez, Moises A. Rocha-Muñoz, Alberto D. Zavala-Cerna, Maria G. Front Neurol Neuroscience PURPOSE: To describe a case of optic neuropathy as a primary manifestation of polyarteritis nodosa (PAN) and discuss diagnostic challenges. METHODS: Case report. RESULTS: A 41-year-old Hispanic man presented with a 2-day history of reduced visual acuity in his left eye. Physical examination revealed a complete visual field loss in the affected eye. Best-corrected visual acuity (BCVA) in the left eye was hand motion, and fundus examination revealed a hyperemic optic disk with blurred margins, swelling, retinal folds, dilated veins, and normal size arteries. BCVA in the right eye was 20/20; no anomalies were seen during examination of the fundus. The patient was started on oral corticosteroids and once the diagnosis of PAN was made, cyclophosphamide was added to the treatment regimen. Six months later, the patient recovered his BCVA to 20/20 in his left eye. CONCLUSION: Rarely does optic neuropathy present as a primary manifestation of PAN; nevertheless, it represents an ophthalmologic emergency that requires expeditious anti-inflammatory and immunosuppressive treatment to decrease the probability of permanent visual damage. Unfortunately, diagnosing PAN is challenging as it necessitates a high index of suspicion. In young male patients who present for the first time with diminished visual acuity, ophthalmologists become cornerstones in the suspicion of this diagnosis and should be responsible for continuing the study until a diagnosis is reached to ensure rapid commencement of immunosuppressive treatment. Frontiers Media S.A. 2017-09-20 /pmc/articles/PMC5611380/ /pubmed/28979236 http://dx.doi.org/10.3389/fneur.2017.00490 Text en Copyright © 2017 Vazquez-Romo, Rodriguez-Hernandez, Paczka, Nuño-Suarez, Rocha-Muñoz and Zavala-Cerna. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Vazquez-Romo, Kristian A.
Rodriguez-Hernandez, Adrian
Paczka, Jose A.
Nuño-Suarez, Moises A.
Rocha-Muñoz, Alberto D.
Zavala-Cerna, Maria G.
Optic Neuropathy Secondary to Polyarteritis Nodosa, Case Report, and Diagnostic Challenges
title Optic Neuropathy Secondary to Polyarteritis Nodosa, Case Report, and Diagnostic Challenges
title_full Optic Neuropathy Secondary to Polyarteritis Nodosa, Case Report, and Diagnostic Challenges
title_fullStr Optic Neuropathy Secondary to Polyarteritis Nodosa, Case Report, and Diagnostic Challenges
title_full_unstemmed Optic Neuropathy Secondary to Polyarteritis Nodosa, Case Report, and Diagnostic Challenges
title_short Optic Neuropathy Secondary to Polyarteritis Nodosa, Case Report, and Diagnostic Challenges
title_sort optic neuropathy secondary to polyarteritis nodosa, case report, and diagnostic challenges
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611380/
https://www.ncbi.nlm.nih.gov/pubmed/28979236
http://dx.doi.org/10.3389/fneur.2017.00490
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