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Bilateral Cerebral Mucormycosis in an Immunocompetent Female.

Authors :
Okwechime, Remi T.
Reyes, Nicholas
Trivedi, Darshan
Iwuchukwu, Ifeanyi O.
Source :
Ochsner Journal. Jun2022, Vol. 22 Issue 2, p169-175. 7p.
Publication Year :
2022

Abstract

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 biopsywith 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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15245012
Volume :
22
Issue :
2
Database :
Academic Search Index
Journal :
Ochsner Journal
Publication Type :
Academic Journal
Accession number :
157536581
Full Text :
https://doi.org/10.31486/toj.21.0088