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An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis

An 82‐year‐old man, who was healthy and had worked as a farmer, experienced worsening neurological symptoms over a seven‐month period, which eventually caused his death. Multiple fluctuating brain lesions were detected radiographically. Clinically, sarcoidosis was ranked high among the differential...

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Autores principales: Maehara, Tatsuro, Mizuno, Tetsushi, Tokoro, Masaharu, Hara, Tatsuru, Tomita, Yui, Makioka, Kouki, Motegi, Sei‐Ichiro, Yamazaki, Ayako, Matsumura, Nozomi, Nobusawa, Sumihito, Yokoo, Hideaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546287/
https://www.ncbi.nlm.nih.gov/pubmed/35165936
http://dx.doi.org/10.1111/neup.12798
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author Maehara, Tatsuro
Mizuno, Tetsushi
Tokoro, Masaharu
Hara, Tatsuru
Tomita, Yui
Makioka, Kouki
Motegi, Sei‐Ichiro
Yamazaki, Ayako
Matsumura, Nozomi
Nobusawa, Sumihito
Yokoo, Hideaki
author_facet Maehara, Tatsuro
Mizuno, Tetsushi
Tokoro, Masaharu
Hara, Tatsuru
Tomita, Yui
Makioka, Kouki
Motegi, Sei‐Ichiro
Yamazaki, Ayako
Matsumura, Nozomi
Nobusawa, Sumihito
Yokoo, Hideaki
author_sort Maehara, Tatsuro
collection PubMed
description An 82‐year‐old man, who was healthy and had worked as a farmer, experienced worsening neurological symptoms over a seven‐month period, which eventually caused his death. Multiple fluctuating brain lesions were detected radiographically. Clinically, sarcoidosis was ranked high among the differential diagnoses because of the presence of skin lesions showing granulomatous inflammation, confirmed by biopsy. The patient's cerebrospinal fluid was also examined, but no definitive diagnosis was made while he was alive. An autopsy revealed multiple granulomatous amebic encephalitis lesions in the brain. Genetic and immunohistochemical analyses identified Balamuthia (B.) mandrillaris, a free‐living ameba, which resides in soil and fresh water, as the causative organism. A retrospective examination revealed B. mandrillaris in the biopsied skin as well as cerebrospinal fluid, strongly suggesting that the ameba had spread into the brain percutaneously. Few studies have detailed the cutaneous pathology of B. mandrillaris infections. In general, granulomatous amebic encephalitis is extremely difficult to diagnose without autopsy, but the present case provides a clue that could allow similar cases to be diagnosed earlier; that is, the presence of skin lesions.
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spelling pubmed-95462872022-10-14 An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis Maehara, Tatsuro Mizuno, Tetsushi Tokoro, Masaharu Hara, Tatsuru Tomita, Yui Makioka, Kouki Motegi, Sei‐Ichiro Yamazaki, Ayako Matsumura, Nozomi Nobusawa, Sumihito Yokoo, Hideaki Neuropathology Case Reports An 82‐year‐old man, who was healthy and had worked as a farmer, experienced worsening neurological symptoms over a seven‐month period, which eventually caused his death. Multiple fluctuating brain lesions were detected radiographically. Clinically, sarcoidosis was ranked high among the differential diagnoses because of the presence of skin lesions showing granulomatous inflammation, confirmed by biopsy. The patient's cerebrospinal fluid was also examined, but no definitive diagnosis was made while he was alive. An autopsy revealed multiple granulomatous amebic encephalitis lesions in the brain. Genetic and immunohistochemical analyses identified Balamuthia (B.) mandrillaris, a free‐living ameba, which resides in soil and fresh water, as the causative organism. A retrospective examination revealed B. mandrillaris in the biopsied skin as well as cerebrospinal fluid, strongly suggesting that the ameba had spread into the brain percutaneously. Few studies have detailed the cutaneous pathology of B. mandrillaris infections. In general, granulomatous amebic encephalitis is extremely difficult to diagnose without autopsy, but the present case provides a clue that could allow similar cases to be diagnosed earlier; that is, the presence of skin lesions. John Wiley & Sons Australia, Ltd 2022-02-14 2022-06 /pmc/articles/PMC9546287/ /pubmed/35165936 http://dx.doi.org/10.1111/neup.12798 Text en © 2022 The Authors. Neuropathology published by John Wiley & Sons Australia, Ltd on behalf of Japanese Society of Neuropathology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Reports
Maehara, Tatsuro
Mizuno, Tetsushi
Tokoro, Masaharu
Hara, Tatsuru
Tomita, Yui
Makioka, Kouki
Motegi, Sei‐Ichiro
Yamazaki, Ayako
Matsumura, Nozomi
Nobusawa, Sumihito
Yokoo, Hideaki
An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis
title An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis
title_full An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis
title_fullStr An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis
title_full_unstemmed An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis
title_short An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis
title_sort autopsy case of granulomatous amebic encephalitis caused by balamuthia mandrillaris involving prior amebic dermatitis
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546287/
https://www.ncbi.nlm.nih.gov/pubmed/35165936
http://dx.doi.org/10.1111/neup.12798
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