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Pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP)

BACKGROUND: Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is an early onset dementia characterized by axonal loss in the cerebral white matter with swollen axons (spheroids). It had been reported that the preferential thinning and “focal lesions” of the corpus callo...

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Autores principales: Kinoshita, Michiaki, Oyanagi, Kiyomitsu, Kondo, Yasufumi, Ishizawa, Keisuke, Ishihara, Kenji, Yoshida, Mari, Inoue, Teruhiko, Mitsuyama, Yoshio, Yoshida, Kunihiro, Yamada, Mitsunori, Sekijima, Yoshiki, Ikeda, Shu-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844436/
https://www.ncbi.nlm.nih.gov/pubmed/33553700
http://dx.doi.org/10.1016/j.ensci.2021.100310
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author Kinoshita, Michiaki
Oyanagi, Kiyomitsu
Kondo, Yasufumi
Ishizawa, Keisuke
Ishihara, Kenji
Yoshida, Mari
Inoue, Teruhiko
Mitsuyama, Yoshio
Yoshida, Kunihiro
Yamada, Mitsunori
Sekijima, Yoshiki
Ikeda, Shu-ichi
author_facet Kinoshita, Michiaki
Oyanagi, Kiyomitsu
Kondo, Yasufumi
Ishizawa, Keisuke
Ishihara, Kenji
Yoshida, Mari
Inoue, Teruhiko
Mitsuyama, Yoshio
Yoshida, Kunihiro
Yamada, Mitsunori
Sekijima, Yoshiki
Ikeda, Shu-ichi
author_sort Kinoshita, Michiaki
collection PubMed
description BACKGROUND: Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is an early onset dementia characterized by axonal loss in the cerebral white matter with swollen axons (spheroids). It had been reported that the preferential thinning and “focal lesions” of the corpus callosum were observed on T2-weighted MRI in ALSP patients. The present study aimed to reveal the pathologic basis of them in relation to brain lesion staging (I ~ IV: Oyanagi et al. 2017). METHODS: Seven autopsied brains of ALSP and five controls were neuropathologically examined. RESULTS: Even at Stage I, corpus callosum body showed evident atrophy, and the atrophy advanced with stage progression. Spheroid size and density were maximal at Stage II in both centrum semiovale and corpus callosum body, but spheroids were larger in corpus callosum body than in centrum semiovale. Microglia in the body at Stage II had a larger cytoplasm than those in centrum semiovale. But spheroids and microglia in the “focal lesions” were identical with those of centrum semiovale. CONCLUSION: Preferential thinning of corpus callosum was considered to be formed in relation to peculiar morphological alteration of microglia there in ALSP. Instead, “focal lesions” were formed in connection with the lesions in centrum semiovale.
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spelling pubmed-78444362021-02-04 Pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) Kinoshita, Michiaki Oyanagi, Kiyomitsu Kondo, Yasufumi Ishizawa, Keisuke Ishihara, Kenji Yoshida, Mari Inoue, Teruhiko Mitsuyama, Yoshio Yoshida, Kunihiro Yamada, Mitsunori Sekijima, Yoshiki Ikeda, Shu-ichi eNeurologicalSci Original Article BACKGROUND: Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is an early onset dementia characterized by axonal loss in the cerebral white matter with swollen axons (spheroids). It had been reported that the preferential thinning and “focal lesions” of the corpus callosum were observed on T2-weighted MRI in ALSP patients. The present study aimed to reveal the pathologic basis of them in relation to brain lesion staging (I ~ IV: Oyanagi et al. 2017). METHODS: Seven autopsied brains of ALSP and five controls were neuropathologically examined. RESULTS: Even at Stage I, corpus callosum body showed evident atrophy, and the atrophy advanced with stage progression. Spheroid size and density were maximal at Stage II in both centrum semiovale and corpus callosum body, but spheroids were larger in corpus callosum body than in centrum semiovale. Microglia in the body at Stage II had a larger cytoplasm than those in centrum semiovale. But spheroids and microglia in the “focal lesions” were identical with those of centrum semiovale. CONCLUSION: Preferential thinning of corpus callosum was considered to be formed in relation to peculiar morphological alteration of microglia there in ALSP. Instead, “focal lesions” were formed in connection with the lesions in centrum semiovale. Elsevier 2021-01-22 /pmc/articles/PMC7844436/ /pubmed/33553700 http://dx.doi.org/10.1016/j.ensci.2021.100310 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Kinoshita, Michiaki
Oyanagi, Kiyomitsu
Kondo, Yasufumi
Ishizawa, Keisuke
Ishihara, Kenji
Yoshida, Mari
Inoue, Teruhiko
Mitsuyama, Yoshio
Yoshida, Kunihiro
Yamada, Mitsunori
Sekijima, Yoshiki
Ikeda, Shu-ichi
Pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP)
title Pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP)
title_full Pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP)
title_fullStr Pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP)
title_full_unstemmed Pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP)
title_short Pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP)
title_sort pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (alsp)
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844436/
https://www.ncbi.nlm.nih.gov/pubmed/33553700
http://dx.doi.org/10.1016/j.ensci.2021.100310
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