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Isolated neuroparacoccidioidomycosis as a pseudotumoral lesion in the absence of systemic disease
BACKGROUND: Paracoccidioidomycosis (PCM) is a systemic, progressive, noncontagious, and often chronic disease caused by the fungus Paracoccidioides brasiliensis that rarely affects the central nervous system (CNS). The condition is usually treated using antifungal drugs, and some cases may require s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Scientific Scholar
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332495/ https://www.ncbi.nlm.nih.gov/pubmed/32637204 http://dx.doi.org/10.25259/SNI_224_2020 |
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author | Riechelmann, Ricardo Salemi Rodrigues, Leonardo Henrique Avelar, Tiago Marques Xander, Paulo Adolfo da Costa, Guilherme Henrique Cannoni, Luiz Fernando de Aguiar, Guilherme Brasileiro Veiga, Jose Carlos |
author_facet | Riechelmann, Ricardo Salemi Rodrigues, Leonardo Henrique Avelar, Tiago Marques Xander, Paulo Adolfo da Costa, Guilherme Henrique Cannoni, Luiz Fernando de Aguiar, Guilherme Brasileiro Veiga, Jose Carlos |
author_sort | Riechelmann, Ricardo Salemi |
collection | PubMed |
description | BACKGROUND: Paracoccidioidomycosis (PCM) is a systemic, progressive, noncontagious, and often chronic disease caused by the fungus Paracoccidioides brasiliensis that rarely affects the central nervous system (CNS). The condition is usually treated using antifungal drugs, and some cases may require surgery. CASE DESCRIPTION: A 55-year-old man, a smoker, without known comorbidities, was referred to the neurosurgery team with a history of a single epileptic seizure a week before hospital admission followed by progressive right- sided hemiparesis. Head computed tomography and brain magnetic resonance imaging showed an intra-axial expansive lesion affecting the left parietal lobe, associated with extensive edema and a regional compressive effect producing slight subfalcine herniation that was initially managed as an abscess. After the failure of antibiotic treatment, the patient underwent a neurosurgical procedure for excision of the lesion. Histopathological analysis revealed that it was PCM and there was no evidence of impairment of other systems due to the disease. CONCLUSION: PCM can be a serious, debilitating disease and is potentially fatal. Although isolated CNS involvement is rare, it must be considered, especially in endemic areas, as late diagnosis and treatment severely decreases good outcome rates. |
format | Online Article Text |
id | pubmed-7332495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-73324952020-07-06 Isolated neuroparacoccidioidomycosis as a pseudotumoral lesion in the absence of systemic disease Riechelmann, Ricardo Salemi Rodrigues, Leonardo Henrique Avelar, Tiago Marques Xander, Paulo Adolfo da Costa, Guilherme Henrique Cannoni, Luiz Fernando de Aguiar, Guilherme Brasileiro Veiga, Jose Carlos Surg Neurol Int Case Report BACKGROUND: Paracoccidioidomycosis (PCM) is a systemic, progressive, noncontagious, and often chronic disease caused by the fungus Paracoccidioides brasiliensis that rarely affects the central nervous system (CNS). The condition is usually treated using antifungal drugs, and some cases may require surgery. CASE DESCRIPTION: A 55-year-old man, a smoker, without known comorbidities, was referred to the neurosurgery team with a history of a single epileptic seizure a week before hospital admission followed by progressive right- sided hemiparesis. Head computed tomography and brain magnetic resonance imaging showed an intra-axial expansive lesion affecting the left parietal lobe, associated with extensive edema and a regional compressive effect producing slight subfalcine herniation that was initially managed as an abscess. After the failure of antibiotic treatment, the patient underwent a neurosurgical procedure for excision of the lesion. Histopathological analysis revealed that it was PCM and there was no evidence of impairment of other systems due to the disease. CONCLUSION: PCM can be a serious, debilitating disease and is potentially fatal. Although isolated CNS involvement is rare, it must be considered, especially in endemic areas, as late diagnosis and treatment severely decreases good outcome rates. Scientific Scholar 2020-06-13 /pmc/articles/PMC7332495/ /pubmed/32637204 http://dx.doi.org/10.25259/SNI_224_2020 Text en Copyright: © 2020 Surgical Neurology International http://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, tweak, 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 Riechelmann, Ricardo Salemi Rodrigues, Leonardo Henrique Avelar, Tiago Marques Xander, Paulo Adolfo da Costa, Guilherme Henrique Cannoni, Luiz Fernando de Aguiar, Guilherme Brasileiro Veiga, Jose Carlos Isolated neuroparacoccidioidomycosis as a pseudotumoral lesion in the absence of systemic disease |
title | Isolated neuroparacoccidioidomycosis as a pseudotumoral lesion in the absence of systemic disease |
title_full | Isolated neuroparacoccidioidomycosis as a pseudotumoral lesion in the absence of systemic disease |
title_fullStr | Isolated neuroparacoccidioidomycosis as a pseudotumoral lesion in the absence of systemic disease |
title_full_unstemmed | Isolated neuroparacoccidioidomycosis as a pseudotumoral lesion in the absence of systemic disease |
title_short | Isolated neuroparacoccidioidomycosis as a pseudotumoral lesion in the absence of systemic disease |
title_sort | isolated neuroparacoccidioidomycosis as a pseudotumoral lesion in the absence of systemic disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332495/ https://www.ncbi.nlm.nih.gov/pubmed/32637204 http://dx.doi.org/10.25259/SNI_224_2020 |
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