| Literature DB >> 18421199 |
Tomoyuki Kakugawa1, Hiroshi Mukae, Masataka Saito, Koji Ishii, Hiroshi Ishimoto, Noriho Sakamoto, Takahiro Takazono, Yuichi Fukuda, Nobuharu Ooe, Shigeru Kohno.
Abstract
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.Entities:
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Year: 2008 PMID: 18421199 DOI: 10.2169/internalmedicine.47.0639
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271