Literature DB >> 26835662

Apical Orbital Aspergillosis Complicating Giant Cell Arteritis.

Yang Zhou1, Michael L Morgan, Sumayya J Almarzouqi, Patricia Chevez-Barrios, Andrew G Lee.   

Abstract

A 75-year-old woman with new onset headaches and left vision loss, temporal scalp tenderness, and jaw claudication was found to have biopsy-proven giant cell arteritis (GCA). Despite treatment and improvement with prednisone, she later developed left orbital apex syndrome, and an orbital biopsy revealed aspergillosis. After antifungal treatment, extraocular motility improved although vision in the left eye remained no light perception. Clinicians should be aware that fungal orbital apex disease may mimic or complicate steroid-treated GCA.

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Year:  2016        PMID: 26835662     DOI: 10.1097/WNO.0000000000000344

Source DB:  PubMed          Journal:  J Neuroophthalmol        ISSN: 1070-8022            Impact factor:   3.042


  2 in total

1.  Blastomyces species and orbital apex syndrome: Unsuspected co-infection.

Authors:  Janice R Safneck; Sherry Krawitz
Journal:  Saudi J Ophthalmol       Date:  2018-02-08

Review 2.  Orbital apex syndrome secondary to aspergilloma masquerading as a paranasal sinus tumor: A case report and literature review.

Authors:  Yu-Min Chang; Yun-Hsiang Chang; Ke-Hung Chien; Chang-Min Liang; Ming-Cheng Tai; Shin Nieh; Ying-Jen Chen
Journal:  Medicine (Baltimore)       Date:  2018-07       Impact factor: 1.889

  2 in total

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