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Orbital aspergillosis: a case report and review of the literature

BACKGROUND: Orbital aspergillosis is a rare sight- and life-threatening fungal infection affecting immunocompromised or otherwise healthy patients. It is often misdiagnosed due to its unspecific clinical and radiologic appearance. Therapeutic delay can have dramatic consequences. However, progress i...

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Autores principales: Lever, Mael, Wilde, Benjamin, Pförtner, Roman, Deuschl, Cornelius, Witzke, Oliver, Bertram, Stefanie, Eckstein, Anja, Rath, Peter-Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792050/
https://www.ncbi.nlm.nih.gov/pubmed/33419395
http://dx.doi.org/10.1186/s12886-020-01773-7
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author Lever, Mael
Wilde, Benjamin
Pförtner, Roman
Deuschl, Cornelius
Witzke, Oliver
Bertram, Stefanie
Eckstein, Anja
Rath, Peter-Michael
author_facet Lever, Mael
Wilde, Benjamin
Pförtner, Roman
Deuschl, Cornelius
Witzke, Oliver
Bertram, Stefanie
Eckstein, Anja
Rath, Peter-Michael
author_sort Lever, Mael
collection PubMed
description BACKGROUND: Orbital aspergillosis is a rare sight- and life-threatening fungal infection affecting immunocompromised or otherwise healthy patients. It is often misdiagnosed due to its unspecific clinical and radiologic appearance. Therapeutic delay can have dramatic consequences. However, progress in microbiological diagnostic techniques and therapeutic experience from case series help improve the management of this disease. CASE PRESENTATION: A 78-year-old immunocompetent woman presented at an eye clinic for subacute swelling, reddening, and ptosis of her left upper eyelid. Based on radiologic and histologic considerations, she was treated for idiopathic orbital inflammation, but her condition worsened. After a second biopsy of the orbital mass, aspergillosis was diagnosed. Her condition improved promptly after initiation of an oral voriconazole treatment. Additionally, using a polymerase chain reaction (PCR) assay, A. fumigatus was identified on tissue of both biopsies and its azole susceptibility was examined simultaneously. CONCLUSIONS: In the case described here, oral antifungal treatment was sufficient for the therapy of invasive orbital aspergillosis. Performing fungal PCR on orbital tissue can accelerate the diagnostic process and should be performed in ambiguous cases of slowly growing orbital mass. Finally, interdisciplinary management is the key to optimal treatment of orbital tumours and infections.
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spelling pubmed-77920502021-01-11 Orbital aspergillosis: a case report and review of the literature Lever, Mael Wilde, Benjamin Pförtner, Roman Deuschl, Cornelius Witzke, Oliver Bertram, Stefanie Eckstein, Anja Rath, Peter-Michael BMC Ophthalmol Case Report BACKGROUND: Orbital aspergillosis is a rare sight- and life-threatening fungal infection affecting immunocompromised or otherwise healthy patients. It is often misdiagnosed due to its unspecific clinical and radiologic appearance. Therapeutic delay can have dramatic consequences. However, progress in microbiological diagnostic techniques and therapeutic experience from case series help improve the management of this disease. CASE PRESENTATION: A 78-year-old immunocompetent woman presented at an eye clinic for subacute swelling, reddening, and ptosis of her left upper eyelid. Based on radiologic and histologic considerations, she was treated for idiopathic orbital inflammation, but her condition worsened. After a second biopsy of the orbital mass, aspergillosis was diagnosed. Her condition improved promptly after initiation of an oral voriconazole treatment. Additionally, using a polymerase chain reaction (PCR) assay, A. fumigatus was identified on tissue of both biopsies and its azole susceptibility was examined simultaneously. CONCLUSIONS: In the case described here, oral antifungal treatment was sufficient for the therapy of invasive orbital aspergillosis. Performing fungal PCR on orbital tissue can accelerate the diagnostic process and should be performed in ambiguous cases of slowly growing orbital mass. Finally, interdisciplinary management is the key to optimal treatment of orbital tumours and infections. BioMed Central 2021-01-08 /pmc/articles/PMC7792050/ /pubmed/33419395 http://dx.doi.org/10.1186/s12886-020-01773-7 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Lever, Mael
Wilde, Benjamin
Pförtner, Roman
Deuschl, Cornelius
Witzke, Oliver
Bertram, Stefanie
Eckstein, Anja
Rath, Peter-Michael
Orbital aspergillosis: a case report and review of the literature
title Orbital aspergillosis: a case report and review of the literature
title_full Orbital aspergillosis: a case report and review of the literature
title_fullStr Orbital aspergillosis: a case report and review of the literature
title_full_unstemmed Orbital aspergillosis: a case report and review of the literature
title_short Orbital aspergillosis: a case report and review of the literature
title_sort orbital aspergillosis: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792050/
https://www.ncbi.nlm.nih.gov/pubmed/33419395
http://dx.doi.org/10.1186/s12886-020-01773-7
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