Fig. 1From: Autoimmune pulmonary alveolar proteinosis developed during immunosuppressive treatment in polymyositis with interstitial lung disease: a case reportClinical course. The patient had no recurrence for fifteen years with immunosuppressive treatment after diagnosis with polymyositis and myositis-associated interstitial pneumonia. In 2019 she was admitted to our hospital complaining progressive dyspnea with increased KL-6.Back to article page