Management of interstitial lung disease in patients with autoimmune disease-related interstitial lung disease

被引：5

作者：

Dsouza, Kevin G. ^{[1
]}

Alexander, Amanda S. ^{[1
]}

Watts Jr, Jubal R. ^{[2
]}

Kulkarni, Tejaswini ^{[1
]}

机构：

[1] Univ Alabama Birmingham, Dept Med, 1900 Univ Blvd,THT 541-D, Birmingham, AL 35294 USA

[2] Univ Alabama Birmingham, Dept Radiol, Birmingham, AL USA

来源：

MULTIDISCIPLINARY RESPIRATORY MEDICINE | 2023年 / 18卷

关键词：

rheumatoid arthritis; dermatomyositis; polymyositis; pulmonary fibrosis; systemic scleroderma; DOUBLE-BLIND; RITUXIMAB; MORTALITY; CYCLOPHOSPHAMIDE; EFFICACY; TERM; PROGRESSION; EXPERIENCE; PREDICTORS; SURVIVAL;

D O I：

10.4081/mrm.2023.890

中图分类号：

R56 [呼吸系及胸部疾病];

学科分类号：

摘要：

Interstitial lung disease (ILD) is a common manifestation of systemic autoimmune diseases. A proportion of patients with autoimmune disease associated-ILDs develop progressive pulmonary fibrosis. Regular monitoring of patients with pulmonary fibrosis is recommended to enable prompt detection of progression and initiation or escalation of therapy if needed. However, there is no established algorithm for the treatment of autoimmune disease associated-ILDs. In this article, we present three case studies that demonstrate the challenges in the diag-nosis and management of patients with autoimmune disease associated-ILDs and the importance of taking a mul-tidisciplinary approach to their care.

引用

页数：10

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