WordNet
- myositis characterized by weakness of limb and neck muscles and much muscle pain and swelling accompanied by skin rash affecting cheeks and eyelids and neck and chest and limbs; progression and severity vary among individuals
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- 1. 成人における皮膚筋炎および多発性筋炎の臨床症状 clinical manifestations of dermatomyositis and polymyositis in adults
- 2. 皮膚筋炎の初期マネージメント initial management of cutaneous dermatomyositis
- 3. 皮膚筋炎および多発性筋炎における間質性肺疾患：臨床症状および診断 interstitial lung disease in dermatomyositis and polymyositis clinical manifestations and diagnosis
- 4. 皮膚筋炎および多発性筋炎における間質性肺疾患：治療 interstitial lung disease in dermatomyositis and polymyositis treatment
- 5. 成人における皮膚筋炎および多発性筋炎の診断および鑑別診断 diagnosis and differential diagnosis of dermatomyositis and polymyositis in adults
English Journal
- HRCT features of interstitial lung disease in dermatomyositis with anti-CADM-140 antibody.
- Tanizawa K, Handa T, Nakashima R, Kubo T, Hosono Y, Watanabe K, Aihara K, Oga T, Chin K, Nagai S, Mimori T, Mishima M.SourceDepartment of Respiratory Medicine, Graduate School of Medicine, Kyoto University, 54 Shogoin Kawaharacho, Sakyo-ku, Kyoto 606-8507, Japan.
- Respiratory medicine.Respir Med.2011 May 30. [Epub ahead of print]
- BACKGROUND: Anti-CADM-140 antibody (anti-CADM-140), also referred to as anti-melanoma differentiation-associated gene 5 (MDA5) antibody, is a myositis-specific antibody identified in the sera of patients with clinically amyopathic dermatomyositis (C-ADM) and is associated with a worse prognosis in d
- PMID 21632230
- Longterm Survival and Associated Risk Factors in Patients with Adult-onset Idiopathic Inflammatory Myopathies and Amyopathic Dermatomyositis: Experience in a Single Institute in Japan.
- Yamasaki Y, Yamada H, Ohkubo M, Yamasaki M, Azuma K, Ogawa H, Mizushima M, Ozaki S.SourceFrom the Division of Rheumatology and Allergology, Department of Internal Medicine, St. Marianna University, School of Medicine, Kawasaki, Japan.
- The Journal of rheumatology.J Rheumatol.2011 May 15. [Epub ahead of print]
- OBJECTIVE: To analyze clinical characteristics, survival, causes of death, and risk factors associated with mortality in patients with adult-onset idiopathic inflammatory myopathies (IIM) in Japan.METHODS: We retrospectively investigated 197 patients diagnosed with adult-onset IIM at our hospital fr
- PMID 21572147
Japanese Journal
- 症例 縦隔気腫,皮膚潰瘍を併発し死の転帰をとった間質性肺炎合併Clinically Amyopathic Dermatomyositisの1例
- 内海 大介,松浦 浩徳,林 宏明 [他]
- 西日本皮膚科 72(6), 569-576, 2010-12
- NAID 40017432656
- 多発性筋炎・皮膚筋炎 (特集 膠原病--その入り口から慢性期まで) -- (各論--診断と治療の実際)
- 三森 明夫
- 診断と治療 98(10), 1627-1631, 2010-10
- NAID 40017345170
Related Links
- A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Amyopathic dermatomyositis ... Medscape Reference provides information on this ...
- Amyopathic dermatomyositis (ADM) is a rare condition characterized by skin lesions suggestive of dermatomyositis (DM) without detectable muscle abnormalities af ... Systemic glucocorticoid therapy was given (500-mg solumedrol ...
- 綜 説 多発筋炎・皮膚筋炎 ～難治性病態とその治療戦略～ 下 島 恭 弘 信州大学医学部脳神経内科，リウマチ・膠原病内科 Polymyositis and Dermatomyositis Therapeutic Strategy for Refractory Cases Yasuhiro SHIMOJIMA Department ...
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★リンクテーブル★
| リンク元 | 「無筋炎型皮膚筋炎」「ADM」 |
「無筋炎型皮膚筋炎」
- 英
- amyopathic dermatomyositis
- 同
- ADM、dermatomyositis sine myositis。無筋症型皮膚筋炎、非ミオパチー性皮膚筋炎