抗合成酶综合征与结核分枝杆菌感染有关,表现为急性呼吸衰竭

A. B. Mansour, S. Ben Saad, S. Yaâlaoui, H. Bellali, H. Daghfous, F. Tritar
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引用次数: 0

摘要

抗合成酶综合征(ASS)以肌炎、肺间质性疾病、雷诺现象、发热和机械性手为特征。诊断是通过检测一种针对抗氨基酰基转移rna合成酶(ARS)的抗体来证实的。最常见的抗ars抗体是抗jo - 1。机会性感染是自身免疫性疾病患者死亡的常见原因。免疫抑制治疗进一步增加了感染的风险。我们报告一个罕见的病例68岁的男子诊断为抗合成酶综合征与肺结核感染,揭示了急性呼吸衰竭。这种罕见的结缔组织疾病和肺结核合并急性呼吸衰竭的诊断是困难的,在一个以前无症状的病人。早期诊断和免疫抑制治疗与抗结核治疗相关的早开始预防疾病进展并产生良好的结果。
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Antisynthetase Syndrome associated with mycobacterium tuberculosis infection, presenting as an acute respiratory failure
Antisynthetase syndrome (ASS) is characterized by myositis, interstitial lung disease, Raynaud’s phenomenon, fever and mechanics hands. Diagnosis is confirmed with the detection of an antibody directed against anti–aminoacyl–transfer–RNA synthetases (ARS). The most common anti–ARS antibody is anti–Jo–1. Opportunistic infections are common causes of mortality in patients with autoimmune diseases. Immunosuppressive treatment further contributes to the risk of infection. We report a rare case of a 68 year–old man diagnosed with antisynthetase syndrome associated to a pulmonary tuberculosis infection, revealed with an acute respiratory failure. The diagnosis of this rare combination of a connective tissue disease and tuberculosis revealed with an acute respiratory failure is difficult in a previously asymptomatic patient. Early diagnosis and immunosuppressive therapy associated to antituberculosis treatment started precociously prevented the disease progression and resulted in a good outcome.
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