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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...

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Autores principales: Okwechime, Remi T., Reyes, Nicholas, Trivedi, Darshan, Iwuchukwu, Ifeanyi O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Division of Ochsner Clinic Foundation 2022
Materias:
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.
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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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