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对特发性肺纤维化急性加重的新认识 被引量:11

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摘要 特发性肺纤维化(idiopathic pulmonary fibrosis,IPF)是一种原因不明、病变局限于肺部的特殊类型慢性纤维化性间质性肺炎,外科肺活检病理结果显示为普通型间质性肺炎(usual interstitial pneumonia,UIP)的组织改变。通常IPF进展缓慢,但部分患者在病程中可能出现难以预测、暴发性并且常是致命性的快速恶化,患者突然出现临床症状加重和低氧血症,胸部影像学检查显示有新的阴影,但没有感染或心力衰竭等征象,这种现象被称为IPF急性加重或称为IPF的加速期。1990年有研究者首先报道,IPF急性加重的病理改变为在UIP基础上叠加了弥漫性肺损伤(diffuse alveolar damage,DAD),以后有研究者对其临床病程作了详细描述。
作者 张德平 侯杰
出处 《中华结核和呼吸杂志》 CAS CSCD 北大核心 2007年第4期298-300,共3页 Chinese Journal of Tuberculosis and Respiratory Diseases
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参考文献18

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二级参考文献13

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共引文献11

同被引文献143

  • 1于娜,刘知陶,姜莉,康健.特发性肺纤维化急性加重1例并文献复习[J].中国实用内科杂志,2006,26(7):986-988. 被引量:12
  • 2康健,朱元珏.特发性间质性肺炎临床研究的新动向[J].中华结核和呼吸杂志,2007,30(4):241-242. 被引量:5
  • 3Kondoh Y,Taniguchi H, Kawabata Y,et al. Acute exacerbation in idiopathic pulmonary fibrosis. Analysis of clinical and pathologic findings in three cases. Chest, 1993,103 :1808-1812.
  • 4Parambil JG, Myers JL, Ryu JH. Histopathologic features and outcome of patients with acute exacerbation of idiopathic pulmonary fibrosis undergoing surgical lung biopsy. Chest, 2005,128 : 3310- 3315.
  • 5Park IN, Kim DS, Shim TS, et al. Acute exacerbation of interstitial pneumonia other than idiopathic pulmonary fibrosis. Chest ,2007,132:214-220.
  • 6Kim DS, Park JH, Park BK, et al. Acute exacerbation of idiopathic pulmonary fibrosis: frequency and clinical features. Eur Respir J ,2006,27 : 143-150.
  • 7Ambrosini V, Cancellieri A, Chilosi M, et al. Acute exacerbation of idiopathic pulmonary fibrosis : report of a series. Eur Respir J, 2003,22 : 821-826.
  • 8Collard HR, Moore BB, Flaherty KR, et al. Acute exacerbations of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med, 2007,176 : 636-643.
  • 9Parambil JG, Myers JL, Ryu JH. Diffuse alveolar damageuncommon manifestation of pulmonary involvement in patients with connective tissue diseases, Chest, 2006,130:553-558.
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引证文献11

二级引证文献43

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