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Intern Med ; 57(6): 849-853, 2018 Mar 15.
Article in English | MEDLINE | ID: mdl-29225267

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.


Subject(s)
Adenocarcinoma/therapy , Dermatomyositis/therapy , Drug Therapy/methods , Immunotherapy/methods , Lung Diseases, Interstitial/therapy , Lung Neoplasms/therapy , Lung/pathology , Adenocarcinoma/diagnostic imaging , Adenocarcinoma of Lung , Comorbidity , Dermatomyositis/diagnostic imaging , Female , Humans , Lung Diseases, Interstitial/diagnostic imaging , Lung Neoplasms/diagnostic imaging , Male , Middle Aged , Treatment Outcome
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