Paraneoplastic neuromyelitis optica spectrum disorder associated with malignant melanoma: A case report

被引：1

作者：

Morimoto, Toshiki ^{[1
,2
]}

Hayashida, Shotaro ^{[3
]}

Yamasaki, Kei ^{[2
]}

Sasahara, Yosuke ^{[1
,2
]}

Takaki, Tsutomu ^{[1
,2
]}

Yatera, Kazuhiro ^{[2
]}

机构：

[1] Kyushu Rosai Hosp, Dept Internal Med, Fukuoka, Japan

[2] Univ Occupat & Environm Hlth, Dept Resp Med, 1-1 Iseigaoka, Kitakyushu, Fukuoka 8078555, Japan

[3] Kyushu Rosai Hosp, Dept Neurol, Fukuoka, Japan

来源：

THORACIC CANCER | 2021年 / 12卷 / 11期

关键词：

anti‐ aquaporin‐ 4; antibody; malignant melanoma; neuromyelitis optica spectrum disorders; paraneoplastic neurological syndrome;

D O I：

10.1111/1759-7714.13965

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Neuromyelitis optica spectrum disorders (NMOSDs) are autoimmune demyelinating diseases involving the central nervous system, affecting the spinal cord and optic nerves. There are few reports of paraneoplastic NMOSD associated with malignant melanoma. Here, we report a rare case of anti-aquaporin 4 (AQP4) antibody-positive NMOSD associated with malignant melanoma. A 61-year-old Japanese woman was diagnosed with malignant melanoma and lung metastasis four years after a diagnosis of anti-AQP4 antibody-positive NMOSD. When diagnosing and treating patients with NMOSD, physicians should be aware of the development of malignancy for at least several years.

引用

页码：1775 / 1779

页数：5

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