Taipei Medical University

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Chung CL
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------>journal_name=Clin Med
------>paper_name=Secondary pulmonary lymphoma: a case report.
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------>pmid=19637801
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------>fullAbstract=A 61-year-old woman was referred to our hospital because of an abnormal chest X-ray shadow. She was diagnosed as having primary Sjogren~s syndrome based on sicca syndrome, polyclonal hyper-gamma-globulinemia, and positive results for anti-Ro/SS-A and anti-La/SS-B antibodies. Her chest CT scan revealed bilateral ground-glass shadows and septal thickning in the lower lung field (Fig. 2a). Biopsy specimens obtained by video-assisted thoracoscopy (VATS) showed a dense interstitial lymphoid infiltrate, including lymphocytes and plasma cells, predominantly in the alveolar septae (Fig. 3, a-c). Malignant lymphoma was excluded on the basis of immunohistopathological studies (Fig. 4). A diagnosis of lymphoid interstitial pneumonia was made according to the 2002 American Thoracic Society/European Respiratory Society international multidisciplinary consensus classification (International Classification). After administration of prednisolone and azathioprin, the ground-glass shadows on the chest CT rapidly improved (Fig. 2b). The clinico-radiologic-pathologic diagnosis based on the VATS procedure and the International Classification is appropriate and effective for treating collagen vascular disease-associated interstitial lung disease.
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------>authors2=Shao KM
------>authors3=Perng RP
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------>authors=Chung CL
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------>updateTitle=[A rare case of primary Sjogren~s syndrome complicated by secondary lymphoid interstitial pneumonia]
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------>publish_year=1995
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A B C D E F G H I J K L M N O P Q R S T U V W X Y Z