Jantz Michael A, Antony Veena B
Division of Pulmonary and Critical Care Medicine, University of Florida, 1600 SW Archer Road, Room M352, PO Box 100225, Gainesville, FL 32610-0225, USA.
Clin Chest Med. 2006 Jun;27(2):181-91. doi: 10.1016/j.ccm.2005.12.003.
Pleural fibrosis can result from a variety of inflammatory processes. The response of the pleural mesothelial cell to injury and the ability to maintain its integrity are crucial in determining whether normal healing or pleural fibrosis occurs. The pleural mesothelial cell, various cytokines, and disordered fibrin turnover are involved in the pathogenesis of pleural fibrosis. The roles of these mediators in producing pleural fibrosis are examined. This article reviews the most common clinical conditions associated with the development of pleural fibrosis. Fibrothorax and trapped lung are two unique and uncommon consequences of pleural fibrosis. The management of pleural fibrosis, including fibrothorax and trapped lung, is discussed.
胸膜纤维化可由多种炎症过程引起。胸膜间皮细胞对损伤的反应及其维持完整性的能力在决定是正常愈合还是发生胸膜纤维化方面至关重要。胸膜间皮细胞、各种细胞因子以及纤维蛋白周转紊乱都参与了胸膜纤维化的发病机制。本文探讨了这些介质在产生胸膜纤维化中的作用。本文综述了与胸膜纤维化发展相关的最常见临床情况。纤维胸和肺被陷是胸膜纤维化的两种独特且不常见的后果。本文还讨论了胸膜纤维化(包括纤维胸和肺被陷)的治疗。