An autopsy case of polyarteritis nodosa accompanied with multiple immune-specific autoantibodies and rhabdomyolysis

Author:

Takeuchi Masako1,Murakami Takenobu1,Noguchi Naoya2,Tajiri Yuki1,Kishi Masafumi1,Sakuwa Mayuko3,Kuwamoto Satoshi4,Adachi Tadashi5,Hanajima Ritsuko3

Affiliation:

1. Department of Neurology, Tottori Prefectural Kousei Hospital

2. Department of Gastroenterology, Tottori Prefectural Kousei Hospital

3. Division of Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University

4. Department of Pathology, Faculty of Medicine, Tottori University

5. Division of Neuropathology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University

Publisher

Societas Neurologica Japonica

Subject

Neurology (clinical)

Reference18 articles.

1. 1) 伊藤聡.結節性多発動脈炎の診断と治療.日本臨床 2018;76:208-212.

2. 2) Nakamura T, Tomoda K, Yamamura Y, et al. Polyarteritis nodosa limited to calf muscles: a case report and review of the literature. Clin Rheumatol 2003;22:149-153.

3. 3) 駒形嘉紀.結節性多発動脈炎.最新医学 2018;139:190-198.

4. 4) Iida H, Hanaoka H, Asari Y, et al. Rhabdomyolysis in a patient with polyarteritis nodosa. Intern Med 2018;57:101-106.

5. 5) 難病情報センター.結節性多発動脈炎[Internet].東京:厚生労働省;[cited 2021 Nov 16]. Available from: https://www.nanbyou.or.jp/entry/244

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