Oh Si-Hyuck, Yoon Kyeong-Wook, Kim Young-Jin, Lee Sang-Koo
Department of Neurosurgery, Dankook University College of Medicine, Cheonan, Korea.
J Korean Neurosurg Soc. 2013 May;53(5):316-9. doi: 10.3340/jkns.2013.53.5.316. Epub 2013 May 31.
Neuromyelitis optica (NMO) is considered to be a rarer autoimmune disease than multiple sclerosis. It is very difficult to make a diagnosis of MNO for doctors who are not familiar with its clinical features and diagnostic criteria. We report a case of a young female patient who had been suffering motor weakness and radiating pain in both upper extremities. Cervical MRI showed tumorous lesion in spinal cord and performed surgery to remove lesion. We could not find a tumor mass in operation field and final diagnosis was NMO. NMO must be included in the differential diagnosis of lesions to rescue the patient from invasive surgical interventions. More specific diagnostic tools may be necessary for early diagnosis and proper treatment.
视神经脊髓炎(NMO)被认为是一种比多发性硬化症更罕见的自身免疫性疾病。对于不熟悉其临床特征和诊断标准的医生来说,诊断NMO非常困难。我们报告一例年轻女性患者,她双上肢出现肌无力和放射性疼痛。颈椎磁共振成像(MRI)显示脊髓有肿瘤样病变,并进行了手术切除病变。我们在手术视野中未发现肿瘤块,最终诊断为NMO。在病变的鉴别诊断中必须考虑NMO,以避免患者接受侵入性手术干预。早期诊断和恰当治疗可能需要更具特异性的诊断工具。