Sudulagunta Sreenivasa Rao, Sodalagunta Mahesh Babu, Khorram Hadi, Sepehrar Mona, Gonivada Jayadevappa, Noroozpour Zahra, Prasad Nagendra
Columbia Asia Hospital, Bangalore, India.
K.S. Hegde Medical College, Mangalore, India.
Ger Med Sci. 2015 Nov 18;13:Doc22. doi: 10.3205/000226. eCollection 2015.
Neuromyelitis optica (NMO or Devic's syndrome) is a rare relapsing demyelinating disease of the central nervous system (CNS) that mainly affects the spinal cord and optic nerves and shares many clinical and radiological features with multiple sclerosis. The association of NMO with other autoimmune diseases was reported, but very few reports described association with autoimmune thyroid disease. Early differentiation between NMO and multiple sclerosis is very important as the natural course and treatment regimens differ significantly. We report a case of a 50-year-old woman who was admitted initially with vomiting, hiccups and paraesthesias but was not diagnosed with NMO and presented with a severe progression of the disease. The patient was also diagnosed to have autoimmune thyroiditis with lymphocytic infiltration of the thyroid which progressed from hyperthyroidism to hypothyroidism. NMO diagnosis was established with seropositivity for NMO-IgG and MRI showing longitudinally extensive spinal cord lesions (3 or more spinal segments). In spite of treatment, the response was poor due to lack of early diagnosis and aggressive immunosuppressant therapy.
视神经脊髓炎(NMO或德维克综合征)是一种罕见的中枢神经系统(CNS)复发性脱髓鞘疾病,主要影响脊髓和视神经,与多发性硬化症有许多临床和影像学特征。曾有NMO与其他自身免疫性疾病相关的报道,但很少有报道描述其与自身免疫性甲状腺疾病的关联。由于自然病程和治疗方案差异很大,NMO与多发性硬化症的早期鉴别非常重要。我们报告一例50岁女性患者,最初因呕吐、打嗝和感觉异常入院,但未被诊断为NMO,随后病情严重进展。该患者还被诊断患有自身免疫性甲状腺炎,甲状腺有淋巴细胞浸润,病情从甲状腺功能亢进发展为甲状腺功能减退。通过NMO-IgG血清阳性和MRI显示纵向广泛的脊髓病变(3个或更多脊髓节段)确诊为NMO。尽管进行了治疗,但由于缺乏早期诊断和积极的免疫抑制治疗,反应不佳。