Paraneoplastic neuromyelitis optica spectrum disorder: A case report and review of the literature

被引:13
|
作者
Annus, Adam [1 ]
Bencsik, Krisztina [1 ]
Obal, Izabella [1 ]
Kincses, Zsigmond Tamas [1 ,2 ]
Tiszlavicz, Laszlo [3 ]
Hoeftberger, Romana [4 ]
Vecsei, Laszlo [1 ,5 ]
机构
[1] Univ Szeged, Fac Gen Med, Dept Neurol, Szeged, Hungary
[2] St Annes Univ Hosp Brno, Int Clin Res Ctr, Brno, Czech Republic
[3] Univ Szeged, Fac Gen Med, Dept Pathol, Szeged, Hungary
[4] Med Univ Vienna, Inst Neurol, Vienna, Austria
[5] MTA SZTE Neurosci Res Grp, Szeged, Hungary
关键词
Neuromyelitis optica; Aquaporin-4; Paraneoplastic; MULTIPLE-SCLEROSIS; AQUAPORIN-4; ANTIBODIES; EXPRESSION; PATTERN; CANCER; SERUM; IGG;
D O I
10.1016/j.jocn.2017.10.030
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Neuromyelitis optica spectrum disorders (NMOSD) are demyelinating, autoimmune diseases affecting the central nervous system. Typically, recurrent optic neuritis and longitudinal extensive transverse myelitis dominates the clinical picture. In most cases NMOSD are associated with autoantibodies targeting the water channel aquaporin-4 (AQP-4). NMOSD usually present in young adults. Clinical findings suggestive of NMOSD in elderly patients should raise the suspicion of a paraneoplastic etiology. To our knowledge, we report the first case of a 66 year-old female patient with paraneoplastic NMOSD that is associated with squamous cell lung carcinoma. Anti-AQP-4 was present in both the serum and cerebrospinal fluid of the patient. However, immunhistological staining of the malignant tissue did not show presence of AQP-4 on the surface of tumour cells. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7 / 10
页数:4
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