自身免疫性甲状腺炎伴视神经脊髓炎(NMO)

Q1 Medicine GMS German Medical Science Pub Date : 2015-11-18 DOI:10.3205/000226
Sreenivasa Rao Sudulagunta, Mahesh Babu Sodalagunta, Hadi Khorram, Mona Sepehrar, Jayadevappa Gonivada, Zahra Noroozpour, N. Prasad
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引用次数: 4

摘要

视神经脊髓炎(NMO或Devic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,与多发性硬化症具有许多临床和放射学特征。NMO与其他自身免疫性疾病的关联有报道,但很少有报道描述与自身免疫性甲状腺疾病的关联。早期鉴别NMO和多发性硬化症是非常重要的,因为自然病程和治疗方案有很大的不同。我们报告一例50岁的女性,她最初因呕吐、打嗝和感觉异常而入院,但未被诊断为NMO,并表现出疾病的严重进展。患者还被诊断为自身免疫性甲状腺炎伴甲状腺淋巴细胞浸润,并由甲状腺功能亢进发展为甲状腺功能减退。NMO- igg血清阳性,MRI显示纵向广泛的脊髓病变(3个或更多脊柱节段),确定NMO诊断。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,反应很差。
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Autoimmune thyroiditis associated with neuromyelitis optica (NMO)
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.
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来源期刊
GMS German Medical Science
GMS German Medical Science Medicine-Medicine (all)
CiteScore
6.30
自引率
0.00%
发文量
10
审稿时长
11 weeks
期刊最新文献
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