Diffuse interstitial lung disease revealing anti-synthetase syndrome: about two cases

被引:0
作者
El Bouardi, Nizar [1 ,2 ]
Alaoui, Amina [1 ,2 ]
Haloua, Meriem [1 ,2 ]
Lamrani, Youssef [1 ,2 ]
Boubbou, Meryem [1 ,2 ]
Maaroufi, Mustapha [1 ,2 ]
Alami, Baderdine [1 ,2 ]
机构
[1] Ctr Hosp Univ Hassan II, Serv Radiol, Fes, Morocco
[2] Univ Sidi Mohamed Ben Abdellah, Fac Med & Pharm, Fes, Morocco
来源
PAN AFRICAN MEDICAL JOURNAL | 2019年 / 32卷
关键词
Antisynthetases syndrome; diffuse infiltrative lung disease; anti-Jo-1; prognosis; ANTISYNTHETASE SYNDROME; PULMONARY-HYPERTENSION; CLINICAL-FEATURES; POLYMYOSITIS; ANTIBODIES; PROGNOSIS; DERMATOMYOSITIS; INVOLVEMENT;
D O I
10.11604/pamj.2019.32.40.17903
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Anti-synthetase syndrome (ASS) is an inflammatory myopathy commonly associated with pulmonary involvement, especially parenchymal (diffuse infiltrative pneumonitis). Extrathoracic manifestations associated with pulmonary involvement can give an indication to the diagnosis: myalgias, polyarthralgias, Raynaud's syndrome, eiythematous palmar hyperkeratosis with fissures and fever. Given the suggestive clinical and radiological picture, the presence of aminoacyl-transfer RNA (tRNA) synthetase antibodies enables to confirm, in particular, Anti Jo-1 antibody activity. Pulmonary involvement is a major prognostic factor, hence the indication for intensive immunosuppressive therapy based on corticosteroids, immunosuppressive medications or the association among them. A better awareness about this disorder revealed by pulmonary manifestations could enable early and adequate management and to improve patient's prognosis.
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页数:9
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