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Brain paracoccidioidomycosis in an immunosuppressed patient with systemic lupus erythematosus
BACKGROUND: Brain paracoccidioidomycosis (PCM) or neuroparacoccidioidomycosis (NPCM) is a fungal infection of the central nervous system (CNS) caused by Paracoccidioides brasiliensis, a dimorphic fungus. The CNS involvement is through bloodstream dissemination. The association between NPCM and syste...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8720419/ https://www.ncbi.nlm.nih.gov/pubmed/34992898 http://dx.doi.org/10.25259/SNI_1012_2021 |
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author | Kamer, Carolina Pretto, Barbara Janke Livramento, Carlos Rafael da Silva, Rafael Carlos |
author_facet | Kamer, Carolina Pretto, Barbara Janke Livramento, Carlos Rafael da Silva, Rafael Carlos |
author_sort | Kamer, Carolina |
collection | PubMed |
description | BACKGROUND: Brain paracoccidioidomycosis (PCM) or neuroparacoccidioidomycosis (NPCM) is a fungal infection of the central nervous system (CNS) caused by Paracoccidioides brasiliensis, a dimorphic fungus. The CNS involvement is through bloodstream dissemination. The association between NPCM and systemic lupus erythematous (SLE) is rare. However, SLE patients are under risk of opportunistic infections given their immunosuppression status. CASE DESCRIPTION: The aim of this case report is to present a 37-year-old female with diagnosis of SLE who presented with progressive and persistent headache in the past 4 months accompanied by the right arm weakness with general and neurologic examination unremarkable. The computerized tomography of the head showed left extra-axial parietooccipital focal hypoattenuation with adjacent bone erosion. The brain magnetic resonance imaging reported left parietooccipital subdural collection associated with focal leptomeningeal thickening with restriction to diffusion and peripheral contrast enhancement. The patient underwent a left craniotomy and dura mater biopsy showed noncaseous granulomatosis with multinucleated giant cells with rounded birefringent structures positive for silver stain, consistent with PCM. Management with itraconazole 200 mg daily was started with a total of 12 months of treatment, with patient presenting resolution of headache and right arm weakness. CONCLUSION: The diagnosis of NPCM is challenging and a high degree of suspicious should be considered in patients with persistent headache and immunosuppression. |
format | Online Article Text |
id | pubmed-8720419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-87204192022-01-05 Brain paracoccidioidomycosis in an immunosuppressed patient with systemic lupus erythematosus Kamer, Carolina Pretto, Barbara Janke Livramento, Carlos Rafael da Silva, Rafael Carlos Surg Neurol Int Case Report BACKGROUND: Brain paracoccidioidomycosis (PCM) or neuroparacoccidioidomycosis (NPCM) is a fungal infection of the central nervous system (CNS) caused by Paracoccidioides brasiliensis, a dimorphic fungus. The CNS involvement is through bloodstream dissemination. The association between NPCM and systemic lupus erythematous (SLE) is rare. However, SLE patients are under risk of opportunistic infections given their immunosuppression status. CASE DESCRIPTION: The aim of this case report is to present a 37-year-old female with diagnosis of SLE who presented with progressive and persistent headache in the past 4 months accompanied by the right arm weakness with general and neurologic examination unremarkable. The computerized tomography of the head showed left extra-axial parietooccipital focal hypoattenuation with adjacent bone erosion. The brain magnetic resonance imaging reported left parietooccipital subdural collection associated with focal leptomeningeal thickening with restriction to diffusion and peripheral contrast enhancement. The patient underwent a left craniotomy and dura mater biopsy showed noncaseous granulomatosis with multinucleated giant cells with rounded birefringent structures positive for silver stain, consistent with PCM. Management with itraconazole 200 mg daily was started with a total of 12 months of treatment, with patient presenting resolution of headache and right arm weakness. CONCLUSION: The diagnosis of NPCM is challenging and a high degree of suspicious should be considered in patients with persistent headache and immunosuppression. Scientific Scholar 2021-11-30 /pmc/articles/PMC8720419/ /pubmed/34992898 http://dx.doi.org/10.25259/SNI_1012_2021 Text en Copyright: © 2021 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, 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 Kamer, Carolina Pretto, Barbara Janke Livramento, Carlos Rafael da Silva, Rafael Carlos Brain paracoccidioidomycosis in an immunosuppressed patient with systemic lupus erythematosus |
title | Brain paracoccidioidomycosis in an immunosuppressed patient with systemic lupus erythematosus |
title_full | Brain paracoccidioidomycosis in an immunosuppressed patient with systemic lupus erythematosus |
title_fullStr | Brain paracoccidioidomycosis in an immunosuppressed patient with systemic lupus erythematosus |
title_full_unstemmed | Brain paracoccidioidomycosis in an immunosuppressed patient with systemic lupus erythematosus |
title_short | Brain paracoccidioidomycosis in an immunosuppressed patient with systemic lupus erythematosus |
title_sort | brain paracoccidioidomycosis in an immunosuppressed patient with systemic lupus erythematosus |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8720419/ https://www.ncbi.nlm.nih.gov/pubmed/34992898 http://dx.doi.org/10.25259/SNI_1012_2021 |
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