Bibliographic Information
- Other Title
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- 増大特集 ギラン・バレー症候群のすべて-100年の軌跡 ギラン・バレー症候群の末梢神経病理
- ギラン・バレー症候群の末梢神経病理
- ギラン ・ バレー ショウコウグン ノ マッショウ シンケイ ビョウリ
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Description
Guillain-Barré syndrome is composed of two distinct clinicopathological entities: acute inflammatory demyelinating polyradiculoneuropathy (AIDP), and acute motor or motor and sensory axonal neuropathy (AMAN and AMSAN). AIDP is characterized by the patchily distributed demyelinative foci throughout the peripheral nervous system (PNS), whereas in AMAN/AMSAN primary axonal degeneration is observed in the PNS, particularly accentuated at the spinal nerve roots. The aim of this article is to provide an overview of previous findings regarding GBS pathology and thus, to elucidate the pathomechanisms of this life-threatening disorder. The most critical cause for AIDP may be the autoimmune attack on the Schwann cell membrane wrapping the myelinated nerve fibers, and that in AMAN/AMSAN may be an antibody-mediated attack on the axolemma at the nodes of Ranvier.
Journal
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- BRAIN and NERVE
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BRAIN and NERVE 67 (11), 1329-1339, 2015-11-01
株式会社医学書院
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Keywords
Details 詳細情報について
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- CRID
- 1390565159947818112
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- NII Article ID
- 40020652924
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- NII Book ID
- AN00144970
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- ISSN
- 13448129
- 18816096
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- NDL BIB ID
- 026914083
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- PubMed
- 26560948
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- Data Source
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- JaLC
- NDL Search
- CiNii Articles
- OpenAIRE