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Lymphocytic interstitial pneumonia in a patient with Sjögren's syndrome / 영남의대학술지
Article in En | WPRIM | ID: wpr-90947
Responsible library: WPRO
ABSTRACT
Lymphocytic interstitial pneumonia (LIP) is a rare benign lymphoproliferative disorder characterized by diffuse infiltration of the pulmonary parenchymal interstitium by polyclonal lymphocytes and plasma cells. LIP has been associated with a variety of clinical conditions; such as connective tissue disorders and other immune system abnormalities. Treatment usually involves administration of corticosteroids and other immunosuppressants. We report on a 38-year-old female patient who complained of shortness of breath, dry mouth, and dry eyes for more than 1 month, and was positive for Raynaud's phenomenon. Based on surgical biopsy, she was diagnosed as having LIP accompanied by Sjögren's syndrome. The patient was treated with high-dose steroids followed by maintenance therapy for approximately 2 years, and her condition improved.
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Full text: 1 Index: WPRIM Main subject: Plasma Cells / Steroids / Biopsy / Lymphocytes / Adrenal Cortex Hormones / Lung Diseases, Interstitial / Connective Tissue / Dyspnea / Immune System / Immunosuppressive Agents Limits: Adult / Female / Humans Language: En Journal: Yeungnam University Journal of Medicine Year: 2016 Type: Article
Full text: 1 Index: WPRIM Main subject: Plasma Cells / Steroids / Biopsy / Lymphocytes / Adrenal Cortex Hormones / Lung Diseases, Interstitial / Connective Tissue / Dyspnea / Immune System / Immunosuppressive Agents Limits: Adult / Female / Humans Language: En Journal: Yeungnam University Journal of Medicine Year: 2016 Type: Article