Severe interstitial lung disease in a patient with anti-PL7 antisynthetase syndrome

Sebastián Molina-Ríos , Gerardo Quintana-López
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Abstract

Antisynthetase syndrome is a rare disease, with varying degrees of lung, muscle, joint, and skin involvement. Due to the introduction of new diagnostic tests, it is possible to detect the disease earlier and to determine the best treatment strategy. However, in our country the availability of these tests is limited. We present the case of a patient with antisynthetase syndrome associated with anti-PL7 antibodies in whom, thanks to the early identification of these antibodies, timely initiation of treatment for the disease was achieved.

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一名抗PL7抗异烟酸酶综合征患者的严重间质性肺病
抗合成代谢酶综合征是一种罕见疾病,患者的肺部、肌肉、关节和皮肤都会受到不同程度的影响。由于引入了新的诊断检测方法,人们可以更早地发现这种疾病,并确定最佳治疗策略。然而,在我国,这些检测方法的可用性非常有限。我们介绍了一例伴有抗PL7抗体的抗异烟酸酶综合征患者的病例,由于及早发现了这些抗体,该患者得以及时开始接受治疗。
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