Kaarteenaho Riitta, Kinnula Vuokko L
Respiratory Research Unit, Department of Internal Medicine, Centre of Excellence in Research, and Clinical Research Center, Institute of Clinical Medicine, Oulu University Hospital, University of Oulu, P.O. Box 22, 90029 Oulu, Finland.
Pulm Med. 2011;2011:531302. doi: 10.1155/2011/531302. Epub 2010 Nov 2.
It has become obvious that several interstitial lung diseases, and even viral lung infections, can progress rapidly, and exhibit similar features in their lung morphology. The final histopathological feature, common in these lung disorders, is diffuse alveolar damage (DAD). The histopathology of DAD is considered to represent end stage phenomenon in acutely behaving interstitial pneumonias, such as acute interstitial pneumonia (AIP) and acute exacerbations of idiopathic pulmonary fibrosis (IPF). Acute worsening and DAD may occur also in patients with nonspecific interstitial pneumonias (NSIPs), and even in severe viral lung infections where there is DAD histopathology in the lung. A better understanding of the mechanisms underlying the DAD reaction is needed to clarify the treatment for these serious lung diseases. There is an urgent need for international efforts for studying DAD-associated lung diseases, since the prognosis of these patients has been and is still dismal.
显而易见,几种间质性肺疾病,甚至病毒性肺部感染,都可能迅速进展,并在肺部形态上呈现出相似特征。这些肺部疾病共有的最终组织病理学特征是弥漫性肺泡损伤(DAD)。DAD的组织病理学被认为代表了急性间质性肺炎(如急性间质性肺炎(AIP)和特发性肺纤维化(IPF)急性加重)的终末期现象。急性恶化和DAD也可能发生在非特异性间质性肺炎(NSIPs)患者中,甚至在肺部存在DAD组织病理学的严重病毒性肺部感染患者中。需要更好地理解DAD反应的潜在机制,以阐明这些严重肺部疾病的治疗方法。迫切需要国际社会共同努力研究与DAD相关的肺部疾病,因为这些患者的预后一直很差,而且现在仍然不容乐观。