Volume 12, Issue 1 pp. 63-65
CASE REPORT

Lenalidomide-associated progressive multifocal leukoencephalopathy

Kazutaka Nishimura

Corresponding Author

Kazutaka Nishimura

Department of Neurology, Matsudo City General Hospital, Matsudo, Japan

Correspondence

Kazutaka Nishimura, Department of Neurology, Matsudo City General Hospital, 993-1 Sendabori, Matsudo, Chiba 270-2296, Japan.

Email: [email protected]

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Yuta Iwai

Yuta Iwai

Department of Neurology, Matsudo City General Hospital, Matsudo, Japan

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Mariko Yabuki

Mariko Yabuki

Department of Neurosurgery, Matsudo City General Hospital, Matsudo, Japan

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Hiroe Fuse

Hiroe Fuse

Department of Hematology, Matsudo City General Hospital, Matsudo, Japan

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Kazuo Nakamichi

Kazuo Nakamichi

Department of Virology, National Institute of Infectious Diseases, Shinjuku-ku, Japan

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Kenta Takahashi

Kenta Takahashi

Department of Pathology, National Institute of Infectious Diseases, Shinjuku-ku, Japan

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Tadaki Suzuki

Tadaki Suzuki

Department of Pathology, National Institute of Infectious Diseases, Shinjuku-ku, Japan

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Masayuki Saijo

Masayuki Saijo

Department of Virology, National Institute of Infectious Diseases, Shinjuku-ku, Japan

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Takeshi Fukushima

Takeshi Fukushima

Department of Neurology, Matsudo City General Hospital, Matsudo, Japan

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Satoshi Kuwabara

Satoshi Kuwabara

Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan

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First published: 11 July 2020
Citations: 3

Abstract

Background

Lenalidomide, an analogue of thalidomide, is frequently used to treat multiple myeloma (MM). Progressive multifocal leukoencephalopathy (PML) is an infectious disease of the central nervous system caused by the reactivation of the JC polyomavirus. Only a few reports have described PML in patients receiving lenalidomide therapy.

Case presentation

A 76-year-old man with MM presented progressive visual and cognitive impairment during lenalidomide administration. Magnetic resonance imaging showed a lesion in the right parietal lobe. Brain biopsy confirmed the diagnosis of PML. Lenalidomide therapy was discontinued, and oral mefloquine was commenced. He was alive more than 1 year later with mild neurologic decline.

Conclusions

Although rare, lenalidomide-induced PML should be considered in myeloma patients treated with lenalidomide.

CONFLICT OF INTEREST

The authors declare no conflict of interest.

DISCLOSURE

Informed consent was obtained from the patient and his caregiver.

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