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混合性結合組織病(MCTD)に伴う神経筋障害
http://hdl.handle.net/10191/34661
http://hdl.handle.net/10191/34661c9fc0702-f1ba-4022-85b8-af17ad202f56
名前 / ファイル | ライセンス | アクション |
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Item type | 紀要論文 / Departmental Bulletin Paper(1) | |||||
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公開日 | 2015-11-23 | |||||
タイトル | ||||||
タイトル | 混合性結合組織病(MCTD)に伴う神経筋障害 | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | 混合性結合組織病(MCTD)に伴う神経筋障害 | |||||
言語 | ||||||
言語 | jpn | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | mixed connective tissue disease | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | neurological complication | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | myositis | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | 混合性結合組織病 | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | 神経系合併症 | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | 筋炎 | |||||
資源タイプ | ||||||
資源 | http://purl.org/coar/resource_type/c_6501 | |||||
タイプ | departmental bulletin paper | |||||
その他のタイトル | ||||||
その他のタイトル | Neurological Complications in MCTD | |||||
著者 |
李, 宝春
× 李, 宝春× 田中, 恵子× 松原, 奈絵× 湯浅, 龍彦 |
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著者別名 | ||||||
識別子 | 134083 | |||||
識別子Scheme | WEKO | |||||
姓名 | Ri, Baschun | |||||
著者別名 | ||||||
識別子 | 134084 | |||||
識別子Scheme | WEKO | |||||
姓名 | Tanaka, Keiko | |||||
著者別名 | ||||||
識別子 | 134085 | |||||
識別子Scheme | WEKO | |||||
姓名 | Matsubara, Nae | |||||
著者別名 | ||||||
識別子 | 134086 | |||||
識別子Scheme | WEKO | |||||
姓名 | Yuasa, Tatsuhiko | |||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Mixed connective tissue disease(MCTD) is a syndrome with overlapping clinical features of SLE, scleroderma and polymyositis. Multiple organs like skin, joint, muscle, lung, heart, kidney and so on are affected with this entity. Nervous system disorder is one of the important complications in MCTD. We reported four patients with MCTD who had various neurological complications such as trigeminal neuropathy, meningitis, cerebral infarction and polyneuropathy respectively. The percentage of MCTD patients with neurological complications such as trigeminal neuropathy, meningitis, cerebral infarction and polyneuropathy respectively. The percentage of MCTD patients with neurological complications is reported as 10~50%, in which, the trigeminal neuropathy and meningitis are most frequent. Psychosis, convulsion, cerebellar ataxia and progressive stupor are also reported to be seen in MCTD. Myositis is reported to manifest in 70% of MCTD patients. The clinicopathological feature of myositis in MCTD is not clearly differed from pure polymyositis (PM), however the muscle pathology of the myositis in MCTD tend to show more infiltrated inflammatory cells at perimysium than PM, whearas PM shows larger number of muscle fibers with simple necrosis. Neuropathic changes are frequently seen neurophysiologically and pathologically in MCTD. PM is seen in younger age group. The pharyngeal and respiratory muscles are more frequently affected in PM. PM shows higher CK levels at acute stage. In this article, we focused on an unexpectedly high incidence of various neurological complications in MCTD and compared the features of myositits in MCTD with PM. | |||||
書誌情報 |
新潟医学会雑誌 en : 新潟医学会雑誌 巻 104, 号 9, p. 777-782, 発行日 1990-09 |
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出版者 | ||||||
出版者 | 新潟医学会 | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 00290440 | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AN00182415 | |||||
著者版フラグ | ||||||
値 | publisher |