Pure Relapsing Short Myelitis

医学 脊髓炎 多发性硬化 扩大残疾状况量表 脊髓 病变 麦当劳标准 视神经脊髓炎 内科学 外科 胃肠病学
作者
Zélia Poullet,Julie Pique,Adil Maarouf,Clemence Boutiere,Audrey Rico,Sarah Demortiere,Pierre Durozard,Caroline Papeix,E. Maillart,Nicolas Collongues,Xavier Ayrignac,Helene Zephir,Romain Deschamps,Jonathan Ciron,Jean Pelletier,Romain Marignier,Bertrand Audoin
出处
期刊:Neuroimmunology and Neuroinflammation [Ovid Technologies (Wolters Kluwer)]
卷期号:9 (4): e1167-e1167
标识
DOI:10.1212/nxi.0000000000001167
摘要

Background and Objectives Pure relapsing short myelitis with clinical and paraclinical features suggesting multiple sclerosis (MS) has been described recently. Here, we evaluated the existence of this potential new form of MS by retrospectively searching for similar cases in the databases of the French tertiary MS centers. Methods Patients were included based on the present criteria: at least 2 short (<3 vertebral segments) myelitis episodes; minimum follow-up of 3 years; no MS-like brain lesion during all the follow-up; tested negative for both anti–myelin oligodendrocyte glycoprotein and anti–aquaporin 4 antibodies in serum; presence of oligoclonal bands in CSF; and comprehensive workup to exclude alternative diagnoses. Results Eighteen patients fulfilled all criteria. The sex ratio (females/males) was 5/1; the median (range) age at first relapse was 35.5 (25–54) years, the disease duration was 80.5 (50–308) months, and the annualized relapse rate was 0.36 (0.1–0.5). The median (range) number of relapses per patient was 2 (2–5), and the median (range) Expanded Disability Status Scale score at last follow-up was 1 (0–7.5). In CSF, the median (range) protein level was 0.34 g/L (0.18–0.77), and the median (range) number of mononuclear cells was 3 (0–28). Spinal cord MRI demonstrated a median (range) number of 2 (1–5) lesions per examination and 3 [1–7] on the last examination. Fifty-five percent of lesions involved the cervical levels. Secondary progressive evolution occurred in 3 of 18 (17%) patients. Discussion Pure spinal MS could be a rare entity in the MS disease spectrum. However, the existence of a distinct entity in the inflammatory CNS disorders cannot be excluded.

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