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Orbital apex syndrome from bacterial sinusitis without orbital cellulitis

PURPOSE: To describe a case of orbital apex syndrome as a result of isolated bacterial sinusitis. OBSERVATIONS: A 63-year-old woman presented with an orbital apex syndrome from isolated bacterial sinusitis with rapidly declining visual acuity to no light perception. We compared our case with 6 simil...

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Autores principales: Pfeiffer, Margaret L., Merritt, Helen A., Bailey, Lucy A., Richani, Karina, Phillips, Margaret E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814374/
https://www.ncbi.nlm.nih.gov/pubmed/29468204
http://dx.doi.org/10.1016/j.ajoc.2018.01.041
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author Pfeiffer, Margaret L.
Merritt, Helen A.
Bailey, Lucy A.
Richani, Karina
Phillips, Margaret E.
author_facet Pfeiffer, Margaret L.
Merritt, Helen A.
Bailey, Lucy A.
Richani, Karina
Phillips, Margaret E.
author_sort Pfeiffer, Margaret L.
collection PubMed
description PURPOSE: To describe a case of orbital apex syndrome as a result of isolated bacterial sinusitis. OBSERVATIONS: A 63-year-old woman presented with an orbital apex syndrome from isolated bacterial sinusitis with rapidly declining visual acuity to no light perception. We compared our case with 6 similar cases of severe vision loss from isolated bacterial sinusitis. In contrast to previously published cases, our patient presented with good vision yet deteriorated to no light perception despite appropriate treatment. CONCLUSIONS AND IMPORTANCE: Orbital apex syndrome can present as a constellation of cranial neuropathies including optic neuropathy from conditions affecting the orbital apex. Although vision loss remained permanent, prompt initiation of broad-spectrum antibiotics and antifungals and surgical intervention prevented further extension of infection into intracranial structures.
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spelling pubmed-58143742018-02-21 Orbital apex syndrome from bacterial sinusitis without orbital cellulitis Pfeiffer, Margaret L. Merritt, Helen A. Bailey, Lucy A. Richani, Karina Phillips, Margaret E. Am J Ophthalmol Case Rep Brief report PURPOSE: To describe a case of orbital apex syndrome as a result of isolated bacterial sinusitis. OBSERVATIONS: A 63-year-old woman presented with an orbital apex syndrome from isolated bacterial sinusitis with rapidly declining visual acuity to no light perception. We compared our case with 6 similar cases of severe vision loss from isolated bacterial sinusitis. In contrast to previously published cases, our patient presented with good vision yet deteriorated to no light perception despite appropriate treatment. CONCLUSIONS AND IMPORTANCE: Orbital apex syndrome can present as a constellation of cranial neuropathies including optic neuropathy from conditions affecting the orbital apex. Although vision loss remained permanent, prompt initiation of broad-spectrum antibiotics and antifungals and surgical intervention prevented further extension of infection into intracranial structures. Elsevier 2018-01-31 /pmc/articles/PMC5814374/ /pubmed/29468204 http://dx.doi.org/10.1016/j.ajoc.2018.01.041 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 Brief report
Pfeiffer, Margaret L.
Merritt, Helen A.
Bailey, Lucy A.
Richani, Karina
Phillips, Margaret E.
Orbital apex syndrome from bacterial sinusitis without orbital cellulitis
title Orbital apex syndrome from bacterial sinusitis without orbital cellulitis
title_full Orbital apex syndrome from bacterial sinusitis without orbital cellulitis
title_fullStr Orbital apex syndrome from bacterial sinusitis without orbital cellulitis
title_full_unstemmed Orbital apex syndrome from bacterial sinusitis without orbital cellulitis
title_short Orbital apex syndrome from bacterial sinusitis without orbital cellulitis
title_sort orbital apex syndrome from bacterial sinusitis without orbital cellulitis
topic Brief report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814374/
https://www.ncbi.nlm.nih.gov/pubmed/29468204
http://dx.doi.org/10.1016/j.ajoc.2018.01.041
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