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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...

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Autores principales: Kilbourn, Kent J., Green, Jaquise, Zacharewski, Nicholas, Aferzon, Joseph, Lawlor, Michael, Jaffa, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2022
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.
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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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