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Antisynthetase syndrome with stroke

机译:抗中风综合征

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Sir,Antisynthetase syndrome (ASS) is a rare autoimmune disease of unknown etiology. The hallmark of the disorder is the presence of serum autoantibodies, which recognize the aminoacyl-tRNA synthetases, a family of intracytoplasmic enzymes that play a role in protein synthesis.[1] The clinical characteristics of ASS include myositis; interstitial lung disease, and chronic articular involvement either alone or in combination. Involvement of various systems has been reported in ASS, neurological manifestations have not been reported previously.A 52-year-old female presented with acute onset right upper and lower limb weakness 8 hours after onset. She had history of polyarthritis and exertional dyspnea for which she was evaluated and diagnosed as interstitial lung disease and was on irregular treatment with steroids and immunosuppressants. She did not have history suggestive of photosensitivity, Raynaud's phenomenon or myalgia. General examination revealed "mechanic's hands" and respiratory system examination showed fine inspiratory crepitations. Neurological examination revealed conscious and mute patient with grade 3/5 power in right upper limb and grade 0/5 power in right lower limb with National Institute of Health Stroke Scale score of 17.
机译:主席先生,抗合成酶综合症(ASS)是一种病因不明的罕见自身免疫性疾病。该疾病的标志是存在血清自身抗体,该抗体可识别氨酰基-tRNA合成酶,这是一种在蛋白合成中起作用的胞质内酶家族。[1] ASS的临床特征包括肌炎。间质性肺疾病和慢性关节受累,无论是单独还是联合使用。 ASS报道了各种系统的参与,以前没有神经系统表现的报道。一名52岁的女性在发病后8小时出现右上肢和下肢无力的急性发作。她有多关节炎和劳累性呼吸困难的病史,据此评估并诊断为间质性肺病,并接受类固醇和免疫抑制剂的不规则治疗。她没有暗示光敏性,雷诺现象或肌痛的病史。常规检查显示“机械手”,呼吸系统检查显示细小吸气。神经系统检查显示,清醒和安静的患者右上肢3/5级,右下肢0/5级,美国国立卫生研究院卒中量表评分为17。

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