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The Clinical Feature of Microscopic Polyangiitis and Granulomatosis with Polyangiitis Kazuki Kakimoto 1 , Mitsuyuki Murano 2 , Takuya Inoue 1 , Yosuke Abe 1 , Ken Kawakami 1 , Toshihiko Okada 1 , Sadaharu Nouda 1 , Yutaka Naka 1 , Azusa Hara 1 , Yujiro Henmi 1 , Naoko Murano 2 , Toshihisa Takeuchi 1 , Yutaro Egashira 3 , Kazuhide Higuchi 1 1The Second Department of Internal Medicine, Osaka Medical College, Takatsuki, Japan 2Murano Clinic, Osaka, Japan 3The Department of Pathology, Osaka Medical College, Takatsuki, Japan Keyword: 顕微鏡的多発血管炎 , 多発血管炎性肉芽腫症 , Wegener肉芽腫症 , ANCA関連血管炎 pp.1381-1387
Published Date 2015/10/25
DOI https://doi.org/10.11477/mf.1403200446
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 Microscopic polyangiitis and granulomatosis with polyangiitis are vasculitis syndromes that invade minute blood vessels. These diseases are part of AASV(ANCA-associated systemic vasculitides). Some patients with AASV suffer from gastrointestinal lesions. As a feature of gastrointestinal involvement, edematous mucosa, longitudinal ulcers, and erosions are observed on endoscopy. For the proper diagnosis of AASV, it is important to check for systemic disorders because of the poor diagnosis of gastrointestinal lesions by biopsy.


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電子版ISSN 1882-1219 印刷版ISSN 0536-2180 医学書院

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