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Idiopathic pulmonary fibrosis clinical features and diagnosis

机译:特发性肺纤维化的临床特点和诊断

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Idiopathic pulmonary' fibrosis (IPF) is one of many conditions that are grouped together under the term "interstitial lung diseases". Despite considerable heterogeneity in the cause, presentation, treatment options and outcomes of these conditions, the interstitial lung diseases are grouped together because of similarities in clinical and radiological presentation (see Box 1, p221). The complex and historically inconsistent terminology, multitude and relative rarity of individual subtypes of interstitial lung disease contribute to confusion in their diagnosis and description.
机译:特发性肺纤维化(IPF)是在“间质性肺疾病”一词中归类在一起的许多疾病之一。尽管在这些病因,表现,治疗选择和结果方面存在很大的异质性,但由于临床和放射学表现的相似性,间质性肺疾病仍被归类在一起(见专栏1,第221页)。间质性肺病各亚型的术语复杂,历史上不一致,种类繁多和相对稀少,导致其诊断和描述混乱。

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