A case of multifocal acquired demyelinating sensory and motor neuropathy with whole body alopecia
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- Machino Yuka
- Department of Neurology, National Mie Hospital
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- Nakayama Shigeho
- Department of Neurology, National Mie Hospital
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- Tomimoto Hidekazu
- Department of Neurology, Mie University Graduate School of Medicine
Bibliographic Information
- Other Title
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- 全身脱毛症をともなった多巣性脱髄性感覚運動型chronic inflammatory demyelinating polyradiculoneuropathy(CIDP)の1例
- ゼンシン ダツモウショウ オ トモナッタ タソウセイ ダツズイセイカンカク ウンドウガタ chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)ノ 1レイ
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Abstract
A 42 years-old male noticed alopecia in 2006. Three years later, he had loss of hair in the whole body and weakness in the left upper limb. Prednisolone treatment failed to alleviate these symptoms. In 2011, he was diagnosed multifocal acquired demyelinating sensory and motor neuropathy and treated by intravenous immunoglobulin (IVIg), which improved muscle strength eventually. Three years later, he had remitting weakness of the limbs, and thus underwent again IVIg with amelioration of both alopecia and weakness in the limbs. Association of multifocal acquired demyelinating sensory and motor neuropathy and alopecia, and their improvement by immunomodulatory treatment strongly suggest a role of immunological pathomechanism.
Journal
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- Rinsho Shinkeigaku
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Rinsho Shinkeigaku 54 (6), 507-510, 2014
Societas Neurologica Japonica
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Details 詳細情報について
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- CRID
- 1390001205034714112
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- NII Article ID
- 130004505592
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- NII Book ID
- AN00253207
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- COI
- 1:STN:280:DC%2BC2cfovFWktA%3D%3D
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- ISSN
- 18820654
- 0009918X
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- NDL BIB ID
- 025584261
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- PubMed
- 24990836
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed