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Fatal Balamuthia mandrillaris Encephalitis

Balamuthia mandrillaris is a rare cause of granulomatous meningoencephalitis associated with high mortality. We report a 69-year-old Caucasian female who presented with a 3-day history of worsening confusion and difficulty with speech. On admission, she was disoriented and had expressive dysphasia....

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Autores principales: Yohannan, Binoy, Feldman, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374803/
https://www.ncbi.nlm.nih.gov/pubmed/30838148
http://dx.doi.org/10.1155/2019/9315756
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author Yohannan, Binoy
Feldman, Mark
author_facet Yohannan, Binoy
Feldman, Mark
author_sort Yohannan, Binoy
collection PubMed
description Balamuthia mandrillaris is a rare cause of granulomatous meningoencephalitis associated with high mortality. We report a 69-year-old Caucasian female who presented with a 3-day history of worsening confusion and difficulty with speech. On admission, she was disoriented and had expressive dysphasia. Motor examination revealed a right arm pronator drift. Cerebellar examination showed slowing of finger-nose testing on the left. She was HIV-negative, but the absolute CD4 count was low. Neuroimaging showed three cavitary, peripherally enhancing brain lesions, involving the right frontal lobe, the left basal ganglia, and the left cerebellar hemisphere. She underwent right frontal craniotomy with removal of tan, creamy, partially liquefied necrotic material from the brain, consistent with granulomatous amoebic encephalitis on tissue staining. Immunohistochemical studies and PCR tests confirmed infection with Balamuthia mandrillaris. She was started on pentamidine, sulfadiazine, azithromycin, fluconazole, flucytosine, and miltefosine. The postoperative course was complicated by an ischemic stroke, and she died a few weeks later.
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spelling pubmed-63748032019-03-05 Fatal Balamuthia mandrillaris Encephalitis Yohannan, Binoy Feldman, Mark Case Rep Infect Dis Case Report Balamuthia mandrillaris is a rare cause of granulomatous meningoencephalitis associated with high mortality. We report a 69-year-old Caucasian female who presented with a 3-day history of worsening confusion and difficulty with speech. On admission, she was disoriented and had expressive dysphasia. Motor examination revealed a right arm pronator drift. Cerebellar examination showed slowing of finger-nose testing on the left. She was HIV-negative, but the absolute CD4 count was low. Neuroimaging showed three cavitary, peripherally enhancing brain lesions, involving the right frontal lobe, the left basal ganglia, and the left cerebellar hemisphere. She underwent right frontal craniotomy with removal of tan, creamy, partially liquefied necrotic material from the brain, consistent with granulomatous amoebic encephalitis on tissue staining. Immunohistochemical studies and PCR tests confirmed infection with Balamuthia mandrillaris. She was started on pentamidine, sulfadiazine, azithromycin, fluconazole, flucytosine, and miltefosine. The postoperative course was complicated by an ischemic stroke, and she died a few weeks later. Hindawi 2019-01-31 /pmc/articles/PMC6374803/ /pubmed/30838148 http://dx.doi.org/10.1155/2019/9315756 Text en Copyright © 2019 Binoy Yohannan and Mark Feldman. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Yohannan, Binoy
Feldman, Mark
Fatal Balamuthia mandrillaris Encephalitis
title Fatal Balamuthia mandrillaris Encephalitis
title_full Fatal Balamuthia mandrillaris Encephalitis
title_fullStr Fatal Balamuthia mandrillaris Encephalitis
title_full_unstemmed Fatal Balamuthia mandrillaris Encephalitis
title_short Fatal Balamuthia mandrillaris Encephalitis
title_sort fatal balamuthia mandrillaris encephalitis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374803/
https://www.ncbi.nlm.nih.gov/pubmed/30838148
http://dx.doi.org/10.1155/2019/9315756
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