病因不明的间质性肺炎的病理特点及分型。

M Kitaichi
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摘要

目前,有五种病因不明的间质性肺炎(IIP);爸爸,up, BOOP, DIP和LIP。表15总结了5种病因不明间质性肺炎(IIP)的临床病程、预后及类固醇激素治疗效果的特点。在前面提到的52例病因不明的间质性肺炎或IIP中,需要开肺活检进行诊断的病例中,大多数病例(81%)为IPF (UIP),其次是特发性BOOP(13%)。这些数据将有助于了解病因不明的间质性肺炎或IIP病例的临床结果和对类固醇激素治疗的治疗反应,因为特发性UIP进展缓慢,通常对类固醇无反应,而特发性BOOP通常对类固醇激素治疗有反应,甚至可能自发消退。IPF (UIP)的病例应该有革命性的治疗方式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pathologic features and the classification of interstitial pneumonia of unknown etiology.

Currently, five types of interstitial pneumonia of unknown etiology or IIP have been described; DAD, UIP, BOOP, DIP and LIP. A summary of the features of clinical course, prognosis and therapeutic effects to steroid hormone treatment of the five types of interstitial pneumonia of unknown etiology or IIP is given in Table 15). Among the previous mentioned 52 open lung biopsy cases of interstitial pneumonia of unknown etiology or IIP, for which an open lung biopsy was necessary for diagnosis, the majority of those cases (81%) was IPF (UIP) while idiopathic BOOP occurred as the second in frequency (13%). These data will help in understanding the clinical outcome and the therapeutic response to steroid hormone treatment in cases of interstitial pneumonia of unknown etiology or IIP, because idopathic UIP is slowly progressive and usually not responsive to steroid while idiopathic BOOP is usually responsive to steroid hormone treatment and may regress even spontaneously. Cases of IPF (UIP) should have revolutional modalities for therapy.

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