医学
间质性肺病
结缔组织
结缔组织病
病理
特发性肺纤维化
疾病
肺
肺纤维化
重症监护医学
特发性间质性肺炎
纤维化
内科学
自身免疫性疾病
作者
Isabel Mira‐Avendano,Andy Abril,Charles D. Burger,Paul F. Dellaripa,Aryeh Fischer,Michael B. Gotway,Augustine S. Lee,Joyce Lee,Eric L. Matteson,Eunhee S. Yi,Jay H. Ryu
标识
DOI:10.1016/j.mayocp.2018.09.002
摘要
Lung involvement in connective tissue diseases is associated with substantial morbidity and mortality, most commonly in the form of interstitial lung disease, and can occur in any of these disorders. Patterns of interstitial lung disease in patients with connective tissue disease are similar to those seen in idiopathic interstitial pneumonias, such as idiopathic pulmonary fibrosis. It may be difficult to distinguish between the 2 ailments, particularly when interstitial lung disease presents before extrapulmonary manifestations of the underlying connective tissue disease. There are important clinical implications in achieving this distinction. Given the complexities inherent in the management of these patients, a multidisciplinary evaluation is needed to optimize the diagnostic process and management strategies. The aim of this article was to summarize an approach to diagnosis and management based on the opinion of experts on this topic.
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