Cross-Disciplinary Collaboration in Connective Tissue Disease-Related Lung Disease

被引:24
作者
Fischer, Aryeh [1 ]
Richeldi, Luca [2 ]
机构
[1] Natl Jewish Hlth, Div Rheumatol, Denver, CO 80206 USA
[2] Univ Southampton, Dept Clin & Expt Sci, Southampton, Hants, England
关键词
collagen vascular disease; interstitial lung disease; connective tissue disease; COLLAGEN VASCULAR-DISEASE; USUAL INTERSTITIAL PNEUMONIA; IDIOPATHIC PULMONARY-FIBROSIS; SYSTEMIC-SCLEROSIS; BRONCHOALVEOLAR LAVAGE; HISTOPATHOLOGIC PATTERN; SCLERODERMA; FEATURES; MANAGEMENT; DISORDERS;
D O I
10.1055/s-0034-1371530
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Lung disease is a common manifestation of connective tissue disease (CTD) and is associated with significant morbidity and mortality. The evaluation of lung disease, and interstitial lung disease (ILD) in particular, in patients with CTD is complex because of the heterogeneity of the CTDs, the varied types and degrees of severity of ILD encountered, and because ILD can be identified at any point in time in these patients. Cross-disciplinary, thorough evaluations are needed when CTD patients develop ILD or when evaluating ILD patients for the presence of occult CTD. Determining that ILD is associated with an established CTD requires the exclusion of alternative etiologies, and thorough assessments of the clinical features of both the CTD and ILD. The detection of occult CTD in patients with "idiopathic" ILD requires careful attention to the demographic profile, historical clues, subtle physical examination findings, specific autoantibody positivity, radiological and histopathological features, and can be optimized by a multidisciplinary approach that includes rheumatological collaboration. Not all patients with CTD-associated ILD require pharmacological therapy, and management decisions should consider pace and severity of the disease, intra- and extrathoracic features of activity and can be optimized by cross-disciplinary collaboration.
引用
收藏
页码:159 / 165
页数:7
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