Lymphocytic interstitial pneumonia in a patient with mixed connective tissue disease – A case report

研究成果: Article

摘要

Lymphocytic interstitial pneumonia (LIP) is an uncommon interstitial lung disease that is characterized by an interstitial infiltrate of lymphoplasmacytic cells. While idiopathic LIP appears to be extremely rare, most reported cases of LIP have been associated with coexisting immune derangements, particularly autoimmune diseases such as Sjögren's syndrome. In this report, we describe the presentation of LIP in a patient with underlying mixed connective tissue disease.

原文English
頁(從 - 到)12-17
頁數6
期刊Respiratory Medicine Case Reports
25
DOIs
出版狀態Published - 2018 一月 1

指紋

Mixed Connective Tissue Disease
Interstitial Lung Diseases
Idiopathic Interstitial Pneumonias
Autoimmune Diseases

All Science Journal Classification (ASJC) codes

  • Pulmonary and Respiratory Medicine

引用此文

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abstract = "Lymphocytic interstitial pneumonia (LIP) is an uncommon interstitial lung disease that is characterized by an interstitial infiltrate of lymphoplasmacytic cells. While idiopathic LIP appears to be extremely rare, most reported cases of LIP have been associated with coexisting immune derangements, particularly autoimmune diseases such as Sj{\"o}gren's syndrome. In this report, we describe the presentation of LIP in a patient with underlying mixed connective tissue disease.",
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