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Intracranial fungal Cladophialophora bantiana infection in a nonimmunocompromised patient: A case report and review of the literature
BACKGROUND: Cladophialophora bantiana is a dematiaceous fungus that rarely infects the central nervous system (CNS). It is associated with a mortality rate of over 70% despite treatment. CASE DESCRIPTION: An 81-year-old female with a remote history of renal cell carcinoma presented with progressive...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062923/ https://www.ncbi.nlm.nih.gov/pubmed/35509580 http://dx.doi.org/10.25259/SNI_116_2022 |
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author | Kilbourn, Kent J. Green, Jaquise Zacharewski, Nicholas Aferzon, Joseph Lawlor, Michael Jaffa, Matthew |
author_facet | Kilbourn, Kent J. Green, Jaquise Zacharewski, Nicholas Aferzon, Joseph Lawlor, Michael Jaffa, Matthew |
author_sort | Kilbourn, Kent J. |
collection | PubMed |
description | BACKGROUND: Cladophialophora bantiana is a dematiaceous fungus that rarely infects the central nervous system (CNS). It is associated with a mortality rate of over 70% despite treatment. CASE DESCRIPTION: An 81-year-old female with a remote history of renal cell carcinoma presented with progressive headache and an expressive aphasia for 3 days. Computed tomography imaging revealed a left frontotemporal mass with surrounding vasogenic edema. A left frontotemporal craniotomy was performed and cultures revealed C. bantiana. The initial management with IV voriconazole was unsuccessful and the patient had a recurrence of the cranial infection and developed pulmonary abscesses. Following the addition of oral flucytosine, the patient showed a significant improvement with a complete radiographic resolution of both the cranial and pulmonary lesions. CONCLUSION: C. bantiana involving the CNS is a rare and often fatal disease. Surgical management along with standard antifungal treatment may not provide definitive therapy. The addition of flucytosine to IV voriconazole resulted in a positive outcome for this patient who is alive, living independently 1 year from the original diagnosis. In this rare fungal infection, standard antifungal treatment may not provide adequate coverage and the utilization of additional therapy may be required. |
format | Online Article Text |
id | pubmed-9062923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-90629232022-05-03 Intracranial fungal Cladophialophora bantiana infection in a nonimmunocompromised patient: A case report and review of the literature Kilbourn, Kent J. Green, Jaquise Zacharewski, Nicholas Aferzon, Joseph Lawlor, Michael Jaffa, Matthew Surg Neurol Int Case Report BACKGROUND: Cladophialophora bantiana is a dematiaceous fungus that rarely infects the central nervous system (CNS). It is associated with a mortality rate of over 70% despite treatment. CASE DESCRIPTION: An 81-year-old female with a remote history of renal cell carcinoma presented with progressive headache and an expressive aphasia for 3 days. Computed tomography imaging revealed a left frontotemporal mass with surrounding vasogenic edema. A left frontotemporal craniotomy was performed and cultures revealed C. bantiana. The initial management with IV voriconazole was unsuccessful and the patient had a recurrence of the cranial infection and developed pulmonary abscesses. Following the addition of oral flucytosine, the patient showed a significant improvement with a complete radiographic resolution of both the cranial and pulmonary lesions. CONCLUSION: C. bantiana involving the CNS is a rare and often fatal disease. Surgical management along with standard antifungal treatment may not provide definitive therapy. The addition of flucytosine to IV voriconazole resulted in a positive outcome for this patient who is alive, living independently 1 year from the original diagnosis. In this rare fungal infection, standard antifungal treatment may not provide adequate coverage and the utilization of additional therapy may be required. Scientific Scholar 2022-04-22 /pmc/articles/PMC9062923/ /pubmed/35509580 http://dx.doi.org/10.25259/SNI_116_2022 Text en Copyright: © 2022 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Kilbourn, Kent J. Green, Jaquise Zacharewski, Nicholas Aferzon, Joseph Lawlor, Michael Jaffa, Matthew Intracranial fungal Cladophialophora bantiana infection in a nonimmunocompromised patient: A case report and review of the literature |
title | Intracranial fungal Cladophialophora bantiana infection in a nonimmunocompromised patient: A case report and review of the literature |
title_full | Intracranial fungal Cladophialophora bantiana infection in a nonimmunocompromised patient: A case report and review of the literature |
title_fullStr | Intracranial fungal Cladophialophora bantiana infection in a nonimmunocompromised patient: A case report and review of the literature |
title_full_unstemmed | Intracranial fungal Cladophialophora bantiana infection in a nonimmunocompromised patient: A case report and review of the literature |
title_short | Intracranial fungal Cladophialophora bantiana infection in a nonimmunocompromised patient: A case report and review of the literature |
title_sort | intracranial fungal cladophialophora bantiana infection in a nonimmunocompromised patient: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062923/ https://www.ncbi.nlm.nih.gov/pubmed/35509580 http://dx.doi.org/10.25259/SNI_116_2022 |
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