Yeungnam Univ J Med.  2016 Dec;33(2):112-115. 10.12701/yujm.2016.33.2.112.

Lymphocytic interstitial pneumonia in a patient with Sjögren's syndrome

Affiliations
  • 1Division of Pulmonology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea. PMS70@yuhs.ac

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.

Keyword

Lymphocytic interstitial pneumonia; Sjögren's syndrome

MeSH Terms

Adrenal Cortex Hormones
Adult
Biopsy
Connective Tissue
Dyspnea
Female
Humans
Immune System
Immunosuppressive Agents
Lip
Lung Diseases, Interstitial*
Lymphocytes
Lymphoproliferative Disorders
Mouth
Plasma Cells
Steroids
Adrenal Cortex Hormones
Immunosuppressive Agents
Steroids
Full Text Links
  • YUJM
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr