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Neuromyelitis optica (NMO) and autoimmune thyroiditis

机译:视神经脊髓炎(NMO)和自身免疫性甲状腺炎

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Neuromyelitis optica (NMO or Devic's syndrome) is a rare demyelinating disease of the CNS that predominantly affects the spinal cord and optic nerves and shares many clinical and radiological features with multiple sclerosis (MS). The association of NMO with autoimmune thyroiditis has been reported very rarely. Early differentiation between NMO and MS is very important because they have different natural courses and treatment regimens. We report a case regarding a 53-year-old woman who was admitted initially with hiccups and paraesthesias, but was not evaluated during first two episodes and presented with severe progression of NMO. Patient was found to have autoimmune thyroiditis with lymphocytic infiltration of thyroid which progressed to hypothyroidism. NMO was diagnosed with seropositivity for NMO-IgG and longitudinally extensive spinal cord lesions (three or more spinal segments). Patient poorly responded to treatment due to the lack of early diagnosis and aggressive immunosuppressant therapy.
机译:视神经脊髓炎(NMO或Devic综合征)是一种罕见的中枢神经系统脱髓鞘疾病,主要影响脊髓和视神经,并具有多发性硬化症(MS),具有许多临床和放射学特征。 NMO与自身免疫性甲状腺炎的关联非常少见。 NMO和MS的早期区分非常重要,因为它们具有不同的自然疗程和治疗方案。我们报道了一例有关一名53岁女性的病例,该女性最初因打h和感觉异常而入院,但在前两次发作期间未进行评估,并呈现出严重的NMO进展。发现患者患有自身免疫性甲状腺炎,并有甲状腺淋巴细胞浸润,发展为甲状腺功能减退症。 NMO被诊断为NMO-IgG和纵向广泛的脊髓损伤(三个或更多个脊髓节段)具有血清阳性。由于缺乏早期诊断和积极的免疫抑制剂治疗,患者对治疗的反应较差。

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