Pulmonary Hyalinizing Granuloma Detected in a Family Member after Confirmation of Tuberculosis in His Father
スポンサーリンク
概要
- 論文の詳細を見る
Pulmonary hyalinizing granuloma (PHG) is an uncommon lung disease that usually presents as bilateral multiple nodules, and more rarely as a solitary nodule. An exaggerated immune response to antigenic stimuli resulting from infection or an autoimmune process has been suggested as the cause of PHG. Here, we describe a rare case of solitary PHG that was detected in a family member after tuberculosis had been confirmed in his father, without any background of infectious disease or autoimmune abnormality.
- Annals of Thoracic and Cardiovascular Surgery 編集委員会の論文
著者
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Miyamoto Yoshihiro
Department of Arthelosclerosis and Diabetes Melitus, National Cardiovacular Center Research Institut
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Imanishi Naoko
Department Of Thoracic Surgery National Hospital Organization Himeji Medical Center
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Nagai Shinjiro
Department Of Thoracic Surgery Graduate School Of Medicine Kyoto University
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Matsuoka Takahisa
Department Of Surgery I Yamaguchi University School Of Medicine
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Ueda Mitsuhiro
Department Of Agricultural Chemistry College Of Agriculture University Of Osaka Prefecture
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Matsuoka Katsunari
Department Of Thoracic Surgery Nho Himeji Medical Center
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Matsuoka Takahisa
Department of Thoracic Surgery, National Hospital Organization Himeji Medical Center, Hyogo, Japan
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Miyamoto Yoshihiro
Department of Thoracic Surgery, National Hospital Organization Himeji Medical Center, Hyogo, Japan
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