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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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John Wiley & Sons Australia, Ltd
2022
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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. |
format | Online Article Text |
id | pubmed-9546287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
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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