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Making the Diagnosis of Myositis: Lung Biopsy and Interpretation

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Managing Myositis
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Abstract

Myositis-associated lung disease occurs in up to 80% of myositis patients. It has to be distinguished from idiopathic or secondary lung diseases such as infection or aspiration. Histologically, myositis-associated interstitial lung disease shows either an acute lung injury pattern such as diffuse alveolar damage (clinically corresponding to sudden onset and rapidly progressing disease) or chronic fibrosing lung disease (clinically corresponding to insidious onset and slowly progressing disease). Histopathologic features are typically not pathognomonic and require multidisciplinary discussion to arrive at the best possible diagnosis. Acute lung injury patterns usually portend a worse prognosis than chronic lung disease. Diffuse fibrosing lung disease in myositis patients usually carries a better prognosis than idiopathic forms of the same histologic pattern.

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Schneider, F., Chen, P. (2020). Making the Diagnosis of Myositis: Lung Biopsy and Interpretation. In: Aggarwal, R., Oddis, C. (eds) Managing Myositis. Springer, Cham. https://doi.org/10.1007/978-3-030-15820-0_15

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