Department of Laboratory Medicine and Pathology, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.
Ann Neurol. 2010 Nov;68(5):757-61. doi: 10.1002/ana.22121.
We report 12 aquaporin-4 antibody-positive patients (12% of seropositive Mayo Clinic patients identified since 2005) whose initial presenting symptom of neuromyelitis optica was intractable vomiting. The initial evaluation in 75% was gastroenterologic. Vomiting lasted a median of 4 weeks (range, 2 days-80 weeks). Optic neuritis or transverse myelitis developed after vomiting onset in 11 patients (median interval, 11 weeks; range, 1-156). At last evaluation (median, 48 months after vomiting onset), 7 patients fulfilled neuromyelitis optica diagnostic criteria. Our clinical, pathologic and neuroimaging observations suggest the aquaporin-4-rich area postrema may be a first point of attack in neuromyelitis optica.
我们报告了 12 例水通道蛋白-4 抗体阳性患者(自 2005 年以来在梅奥诊所发现的血清阳性患者中的 12%),他们的视神经脊髓炎最初表现为难治性呕吐。75%的患者最初接受的是胃肠病学评估。呕吐持续时间中位数为 4 周(范围:2 天-80 周)。11 例患者(中位间隔 11 周;范围 1-156 周)在呕吐发作后出现视神经炎或横贯性脊髓炎。在最后一次评估(呕吐发作后中位数 48 个月)时,7 例患者符合视神经脊髓炎的诊断标准。我们的临床、病理和神经影像学观察提示,水通道蛋白-4 丰富的后极可能是视神经脊髓炎的第一攻击点。