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• ホーム
• 51巻11号
• 臨床神経, 51：964−966, 2011
• 51巻11号目次

＜シンポジウム12―3＞筋炎研究最近の進歩

封入体筋炎の病態と頻度

鈴木　直輝^1）, 竪山　真規^1）, 割田　仁^1）, 井泉　瑠美子^1）, 西野　一三^2）, 青木正志^1）

^1）東北大学大学院医学系研究科神経内科〔〒980―8574 仙台市青葉区星陵町1―1〕
^2）国立精神・神経医療研究センター疾病研究第一部

Sporadic inclusion body myositis (sIBM) is an intractable and progressive skeletal muscle disease of unknown cause and without effective treatment. The etiology of sIBM is still unknown, however genetic factors, aging, life styles, environmental factors may be involved. sIBM is generally refractory to current therapy, such as steroid or immunosuppressants. To elucidate the pathomechanism of sIBM is the most important way to make therapeutic approach. In this review we estimated the prevalence of sIBM in Japan and discuss the pathomechanism of sIBM.
Full Text of this Article in Japanese PDF (242K)

(臨床神経, 51：964−966, 2011)
key words：封入体筋炎，発症率，筋病理，縁取り空胞，炎症細胞

（受付日：2011年5月19日）