Cargando…

Acute orbital apex syndrome and rhino-orbito-cerebral mucormycosis

PURPOSE: To demonstrate the successful clinical identification and management of rhino-orbital mucormycosis, a fungal infection with a high mortality rate. PATIENTS AND METHODS: A diabetic male patient with a headache and orbital apex syndrome in the right eye was examined using computed tomography...

Descripción completa

Detalles Bibliográficos
Autores principales: Anders, Ursula M, Taylor, Elise J, Martel, Joseph R, Martel, James B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4407820/
https://www.ncbi.nlm.nih.gov/pubmed/25945068
http://dx.doi.org/10.2147/IMCRJ.S83036
_version_ 1782367963254358016
author Anders, Ursula M
Taylor, Elise J
Martel, Joseph R
Martel, James B
author_facet Anders, Ursula M
Taylor, Elise J
Martel, Joseph R
Martel, James B
author_sort Anders, Ursula M
collection PubMed
description PURPOSE: To demonstrate the successful clinical identification and management of rhino-orbital mucormycosis, a fungal infection with a high mortality rate. PATIENTS AND METHODS: A diabetic male patient with a headache and orbital apex syndrome in the right eye was examined using computed tomography (CT) and magnetic resonance imaging (MRI) for a possible fungal infection. Endoscopic surgical resection was performed and a pathology sample was taken. Specimens were prepared with Gömöri methenamine silver and hematoxylin and eosin staining. The patient was treated with liposomal amphotericin B 400 mg daily, followed by posaconazole 400 mg twice daily. RESULTS: CT and MRI revealed a mass of the right sphenoid spreading into the orbit, indicative of a fungal infection. The biopsy confirmed the diagnosis of mucormycosis. Complete recovery of eyelid and oculomotor function was achieved after 10 months of treatment, although the patient continues to suffer from irreversible blindness in the right eye due to optic nerve atrophy. He has been without signs or symptoms of recurrence. CONCLUSION: Patients with rhino-orbito-cerebral mucormycosis need extensive surgical and medical treatment to maximize outcomes. Success requires multidisciplinary management.
format Online
Article
Text
id pubmed-4407820
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-44078202015-05-05 Acute orbital apex syndrome and rhino-orbito-cerebral mucormycosis Anders, Ursula M Taylor, Elise J Martel, Joseph R Martel, James B Int Med Case Rep J Case Report PURPOSE: To demonstrate the successful clinical identification and management of rhino-orbital mucormycosis, a fungal infection with a high mortality rate. PATIENTS AND METHODS: A diabetic male patient with a headache and orbital apex syndrome in the right eye was examined using computed tomography (CT) and magnetic resonance imaging (MRI) for a possible fungal infection. Endoscopic surgical resection was performed and a pathology sample was taken. Specimens were prepared with Gömöri methenamine silver and hematoxylin and eosin staining. The patient was treated with liposomal amphotericin B 400 mg daily, followed by posaconazole 400 mg twice daily. RESULTS: CT and MRI revealed a mass of the right sphenoid spreading into the orbit, indicative of a fungal infection. The biopsy confirmed the diagnosis of mucormycosis. Complete recovery of eyelid and oculomotor function was achieved after 10 months of treatment, although the patient continues to suffer from irreversible blindness in the right eye due to optic nerve atrophy. He has been without signs or symptoms of recurrence. CONCLUSION: Patients with rhino-orbito-cerebral mucormycosis need extensive surgical and medical treatment to maximize outcomes. Success requires multidisciplinary management. Dove Medical Press 2015-04-17 /pmc/articles/PMC4407820/ /pubmed/25945068 http://dx.doi.org/10.2147/IMCRJ.S83036 Text en © 2015 Anders et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Case Report
Anders, Ursula M
Taylor, Elise J
Martel, Joseph R
Martel, James B
Acute orbital apex syndrome and rhino-orbito-cerebral mucormycosis
title Acute orbital apex syndrome and rhino-orbito-cerebral mucormycosis
title_full Acute orbital apex syndrome and rhino-orbito-cerebral mucormycosis
title_fullStr Acute orbital apex syndrome and rhino-orbito-cerebral mucormycosis
title_full_unstemmed Acute orbital apex syndrome and rhino-orbito-cerebral mucormycosis
title_short Acute orbital apex syndrome and rhino-orbito-cerebral mucormycosis
title_sort acute orbital apex syndrome and rhino-orbito-cerebral mucormycosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4407820/
https://www.ncbi.nlm.nih.gov/pubmed/25945068
http://dx.doi.org/10.2147/IMCRJ.S83036
work_keys_str_mv AT andersursulam acuteorbitalapexsyndromeandrhinoorbitocerebralmucormycosis
AT taylorelisej acuteorbitalapexsyndromeandrhinoorbitocerebralmucormycosis
AT marteljosephr acuteorbitalapexsyndromeandrhinoorbitocerebralmucormycosis
AT marteljamesb acuteorbitalapexsyndromeandrhinoorbitocerebralmucormycosis