Amyopathic dermatomyositis (ADM) is a clinical subtype of dermatomyositis, characterized by the absence of motor weakness and the presence of normal muscle enzyme levels. ADM is sometimes accompanied by interstitial pneumonia that shows a rapid progressive course associated with a poor prognosis. We describe a 70-year-old man who presented rapidly progressive interstitial pneumonia associated with clinically ADM (C-ADM); he was successfully treated with polymyxin B-immobilized fiber column (PMX) hemoperfusion. © 2008 The Japanese Society of Internal Medicine.
CITATION STYLE
Kakugawa, T., Mukae, H., Saito, M., Ishii, K., Ishimoto, H., Sakamoto, N., … Kohno, S. (2008). Rapidly progressive interstitial pneumonia associated with clinically amyopathic dermatomyositis successfully treated with polymyxin B-immobilized fiber column hemoperfusion. Internal Medicine, 47(8), 785–790. https://doi.org/10.2169/internalmedicine.47.0639
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