CONNECTIVE TISSUE DISEASE ASSOCIATED INTERSTITIAL PNEUMONIA: A CHALLENGE FOR BOTH RHEUMATOLOGISTS AND PULMONOLOGISTS

被引：0
|
作者：
Geerts, Sarah [1 ]
Wuyts, Wim [2 ]
De langhe, Ellen [3 ]
Lenaerts, Jan [3 ]
Yserbyt, Jonas [2 ]
机构：
[1] Katholieke Univ Leuven, Dept Gen Practice, Leuven, Belgium
[2] Univ Hosp Leuven, Dept Pneumol, Leuven, Belgium
[3] Univ Hosp Leuven, Dept Rheumatol, Leuven, Belgium
来源：
SARCOIDOSIS VASCULITIS AND DIFFUSE LUNG DISEASES | 2017年 / 34卷 / 04期
关键词：
connective tissue disease; interstitial lung disease; collagen vascular disease; pulmonary fibrosis; diagnosis; evaluation; treatment; IDIOPATHIC PULMONARY-FIBROSIS; RESOLUTION COMPUTED-TOMOGRAPHY; LUNG-DISEASE; SYSTEMIC-SCLEROSIS; BRONCHOALVEOLAR LAVAGE; SAFETY; PIRFENIDONE; NINTEDANIB; EFFICACY; POLYMYOSITIS;
D O I：
暂无
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) can be either idiopathic, the result of exposure or may be associated with extrapulmonary diseases. Among the latter, connective tissue diseases (CTDs) make up the largest part. The identification, follow-up and treatment of CTD-associated ILD (CTD-ILD) are a challenge for every physician as ILD can occur before, during and after the diagnosis of CTD. Early detection of pulmonary involvement is an essential task for the treating rheumatologist and recognition of the underlying CTD can pose a challenge for the treating pulmonologist. Multidisciplinary engagement towards the patient is therefore indispensable for optimal clinical care.
引用
收藏
页码：326 / 335
页数：10
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