Volume 30, Issue 1 pp. 43-45
Case Report

Immunoadsorption therapy for neuromyelitis optica spectrum disorders long after the acute phase

Masatake Kobayashi

Masatake Kobayashi

Department of Cardiology, Tokyo Medical University, Hachioji Medical Center, Tokyo, Japan

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Kazunori Nanri

Corresponding Author

Kazunori Nanri

Department of Neurology, Tokyo Medical University, Hachioji Medical Center, Tokyo, Japan

Correspondence to: Kazunori Nanri, Department of Neurology, Tokyo Medical University, Hachioji Medical Center, 1163 Tatemachi, Hachioji, Tokyo 193-0998, Japan. E-mail: [email protected].Search for more papers by this author
Takeshi Taguchi

Takeshi Taguchi

Department of Neurology, Tokyo Medical University, Hachioji Medical Center, Tokyo, Japan

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Tomoko Ishiko

Tomoko Ishiko

Department of Neurology, Tokyo Medical University, Hachioji Medical Center, Tokyo, Japan

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Masaharu Yoshida

Masaharu Yoshida

Department of Nephrology, Tokyo Medical University, Hachioji Medical Center, Tokyo, Japan

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Noriko Yoshikawa

Noriko Yoshikawa

Department of Nephrology, Tokyo Medical University, Hachioji Medical Center, Tokyo, Japan

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Kentaro Sugisaki

Kentaro Sugisaki

Department of Nephrology, Tokyo Medical University, Hachioji Medical Center, Tokyo, Japan

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Nobuyuki Tanaka

Nobuyuki Tanaka

Department of Neurology, Tokyo Medical University, Hachioji Medical Center, Tokyo, Japan

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First published: 06 May 2014
Citations: 19

Abstract

Neuromyelitis optica (NMO) is a severe inflammatory demyelinating disease with exacerbations involving recurrent or bilateral optic neuritis and longitudinally extensive transverse myelitis. Pulse steroid therapy is recommended as the initial, acute-phase treatment for NMO. If ineffective, treatment with plasma exchange (PE) should commence. However, no evidence exists to support the effectiveness of PE long after the acute phase. Immunoadsorption therapy (IA) eliminates pathogenic antibodies while sparing other plasma proteins. With IA, side effects of PE resulting from protein substitution can be avoided. However, whether IA is effective for NMO remains unclear. We describe a patient with anti-aquaporin-4-positive myelitis who responded to IA using a tryptophan polyvinyl alcohol gel column that was begun 52 days after disease onset following the acute phase. Even long after the acute phase when symptoms appear to be stable, IA may be effective and should not be excluded as a treatment choice. J. Clin. Apheresis 30:43–45, 2015. © 2014 Wiley Periodicals, Inc.

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