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Bilateral Cerebral Mucormycosis in an Immunocompetent Female
Background: Mucormycosis is a serious angioinvasive fungal infection. Immunocompromised patients are more likely to be susceptible to mucormycosis than immunocompetent individuals. Cerebral mucormycosis has been reported, but cases have primarily been unilateral. We report a case of bilateral cerebr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Academic Division of Ochsner Clinic Foundation
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196963/ https://www.ncbi.nlm.nih.gov/pubmed/35756592 http://dx.doi.org/10.31486/toj.21.0088 |
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author | Okwechime, Remi T. Reyes, Nicholas Trivedi, Darshan Iwuchukwu, Ifeanyi O. |
author_facet | Okwechime, Remi T. Reyes, Nicholas Trivedi, Darshan Iwuchukwu, Ifeanyi O. |
author_sort | Okwechime, Remi T. |
collection | PubMed |
description | Background: Mucormycosis is a serious angioinvasive fungal infection. Immunocompromised patients are more likely to be susceptible to mucormycosis than immunocompetent individuals. Cerebral mucormycosis has been reported, but cases have primarily been unilateral. We report a case of bilateral cerebral mucormycosis in an immunocompetent patient. Case Report: A 37-year-old female with no significant medical history was transferred to our tertiary center after cerebrospinal fluid profile following a lumbar puncture at an outside hospital suggested bacterial meningitis. Computed tomography of the head revealed hypodensity and cerebral edema in the left basal ganglia, and magnetic resonance imaging (MRI) brain showed increased T2 signal and mass-like configuration centered in the left basal ganglia. During her hospital stay, she had neurologic decompensation with respiratory failure. She was intubated and placed on mechanical ventilation. Repeat MRI brain revealed evolving cerebral edema signal and interval development of progression across the midline involving the right basal ganglia. Because of the aggressive nature of the lesion and cerebral edema, she underwent a biopsy with placement of an external ventricular drain. Despite medical and surgical interventions, she neurologically worsened and died. Histopathologic evaluation of the biopsied lesion revealed numerous fungal hyphae consistent with mucormycosis. Conclusion: Our patient was not immunocompromised, and this case highlights the clinical challenges in initiating immunosuppressive therapy in a patient with rapidly progressive central nervous system disease. |
format | Online Article Text |
id | pubmed-9196963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Academic Division of Ochsner Clinic Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-91969632022-06-24 Bilateral Cerebral Mucormycosis in an Immunocompetent Female Okwechime, Remi T. Reyes, Nicholas Trivedi, Darshan Iwuchukwu, Ifeanyi O. Ochsner J Case Reports and Clinical Observations Background: Mucormycosis is a serious angioinvasive fungal infection. Immunocompromised patients are more likely to be susceptible to mucormycosis than immunocompetent individuals. Cerebral mucormycosis has been reported, but cases have primarily been unilateral. We report a case of bilateral cerebral mucormycosis in an immunocompetent patient. Case Report: A 37-year-old female with no significant medical history was transferred to our tertiary center after cerebrospinal fluid profile following a lumbar puncture at an outside hospital suggested bacterial meningitis. Computed tomography of the head revealed hypodensity and cerebral edema in the left basal ganglia, and magnetic resonance imaging (MRI) brain showed increased T2 signal and mass-like configuration centered in the left basal ganglia. During her hospital stay, she had neurologic decompensation with respiratory failure. She was intubated and placed on mechanical ventilation. Repeat MRI brain revealed evolving cerebral edema signal and interval development of progression across the midline involving the right basal ganglia. Because of the aggressive nature of the lesion and cerebral edema, she underwent a biopsy with placement of an external ventricular drain. Despite medical and surgical interventions, she neurologically worsened and died. Histopathologic evaluation of the biopsied lesion revealed numerous fungal hyphae consistent with mucormycosis. Conclusion: Our patient was not immunocompromised, and this case highlights the clinical challenges in initiating immunosuppressive therapy in a patient with rapidly progressive central nervous system disease. Academic Division of Ochsner Clinic Foundation 2022 2022 /pmc/articles/PMC9196963/ /pubmed/35756592 http://dx.doi.org/10.31486/toj.21.0088 Text en ©2022 by the author(s); Creative Commons Attribution License (CC BY) https://creativecommons.org/licenses/by/4.0/©2022 by the author(s); licensee Ochsner Journal, Ochsner Clinic Foundation, New Orleans, LA. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (creativecommons.org/licenses/by/4.0/legalcode) that permits unrestricted use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Case Reports and Clinical Observations Okwechime, Remi T. Reyes, Nicholas Trivedi, Darshan Iwuchukwu, Ifeanyi O. Bilateral Cerebral Mucormycosis in an Immunocompetent Female |
title | Bilateral Cerebral Mucormycosis in an Immunocompetent Female |
title_full | Bilateral Cerebral Mucormycosis in an Immunocompetent Female |
title_fullStr | Bilateral Cerebral Mucormycosis in an Immunocompetent Female |
title_full_unstemmed | Bilateral Cerebral Mucormycosis in an Immunocompetent Female |
title_short | Bilateral Cerebral Mucormycosis in an Immunocompetent Female |
title_sort | bilateral cerebral mucormycosis in an immunocompetent female |
topic | Case Reports and Clinical Observations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9196963/ https://www.ncbi.nlm.nih.gov/pubmed/35756592 http://dx.doi.org/10.31486/toj.21.0088 |
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