Recurring neuromyelitis without optic neuritis: a case report

被引:0
|
作者
Garcia-Rodriguez, Raquel [1 ]
Fernandez-Dominguez, Jessica [1 ]
Gomez-Illan, Rafael [2 ]
Lopez-Roger, Ricardo [2 ]
Mateos, Valentin [1 ]
机构
[1] Ctr Med Asturias, Serv Neurol, E-33193 Oviedo, Asturias, Spain
[2] Ctr Med Asturias, Serv Radiol, E-33193 Oviedo, Asturias, Spain
关键词
Anti-aquaporin-4; Demyelinating; Devic; Longitudinally extensive; Neuromyelitis optica; Recurrence; Transverse myelitis; DIFFERENTIAL-DIAGNOSIS; MYELITIS; SPECTRUM;
D O I
10.33588/rn.5502.2012120
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction. Neuromyelitis optica, or Devic's disease, is an inflammatory, demyelinating disease of the central nervous system that selectively affects the optic nerves and the spinal cord, with a high rate of relapses. Anti-aquaporin-4 (AQP4) antibodies are a highly specific marker for this condition. Case report. A 66-year-old female with longitudinally extensive dorsal transverse myelitis with complete remission following steroidal treatment and later acute relapse, with palsy in one limb. The differential diagnoses considered included a spinal tumour and arteriovenous malformation of the spinal cord. Being positive for AQP4 was the decisive factor in the final diagnosis. Conclusions. Early detection of anti-AQP4 antibodies together with appropriate immunotherapy can be the key to a better prognosis. An early diagnosis is essential to be able to start treatment at an early stage and thus prevent relapses and severe sequelae.
引用
收藏
页码:87 / 90
页数:4
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