Abstract
We herein report the rare case of co-occurring dermatomyositis (DM), interstitial pneumonia (IP), and lung cancer in a 59-year-old man. Computed tomography (CT) and positron emission tomography-CT showed the presence of a left lung tumor with IP, which was diagnosed as lung adenocarcinoma by a CT-guided tumor biopsy. We diagnosed DM based on the presence of myalgia, Gottron’s papules, and anti-aminoacyl-tRNA synthetase antibody positivity in the patient. Co-occurrence of the above-mentioned three diseases is rare, and acute exacerbation of IP is a major cause of death in such cases. These patients can be treated with immunosuppressive therapy followed by chemotherapy.
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Daido, W., Yamasaki, M., Morio, Y., Funaishi, K., Ishiyama, S., Deguchi, N., … Hattori, N. (2018). A rare combination of dermatomyositis, interstitial pneumonia, and lung cancer in a patient treated with immunosuppressive therapy and chemotherapy. Internal Medicine, 57(6), 849–853. https://doi.org/10.2169/internalmedicine.9642-17
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