间质性肺疾病（ILD）是以弥漫性肺实质、肺泡炎症和间质纤维化为病理基本病变，以活动性呼吸困难、X线胸片弥漫性浸润阴影、限制性通气障碍、弥散（DLCO）功能降低和低氧血症为临床表现的不同种类疾病群构成的临床-病理实体的总称。
...肺间质是指肺泡之间的结构，主要包括血管、淋巴管和结缔组织。间质性肺疾病(interstitial lung disease，ILD)是一组异源性疾病，病变发生在两肺肺间质，可累及肺泡上皮细胞、肺毛细血管、动脉和静脉。
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3.2 间质性肺疾病 间质性肺疾病(interstitial pulmonary disease, ILD)是一组异型疾病，早期诊断困难。近年来，应用检测血清SP-A浓度方法诊断间质性肺疾病进展显著。
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弥漫性间质性肺疾病 diffuse interstitial lung disease
也称为间质性肺疾病 interstia lung disease ; ILD
许多间质性肺疾病 interstertial lung disease
其他间质性肺疾病 Other interstitial pulmonary diseases
弥散性肺间质疾病 diffuse intersticial lung disease
肺间质性疾病 interstitial lung disease ; ILD
弥漫性肺间质疾病 diffuse interstitial lung disease ; interstitial lung disease ; diffuse parenchymal lung disease ; DILD
间质性肺部疾病 interstitial lung disease ; ILD
弥漫性肺间质性疾病 interstitial lung disease ; ILD ; Diffuse interstitial lung diseases
Rationale:Idiopathic pulmonary fibrosis (IPF), which is the most common idiopathic interstitial lung disease, has the worse prognosis, with a median survival of only 3 to 4 years.
研究背景与目的:特发性肺纤维化(IPF)是特发性间质性肺疾病最常见的类型,其预后差,生存中位时间仅为3至4年。
参考来源 - HMGB1在肺纤维化中作用的研究·2,447,543篇论文数据，部分数据来源于NoteExpress
间质性肺疾病已观察到异常的患者易瑞沙。
Interstitial lung disease has been observed in patients with abnormal suggested that it should.
肺纤维化是一种由多种因素引起的间质性肺疾病。
AimPulmonary fibrosis is a pulmonary interstitial disease, which is induced by many factors.
如果间质性肺疾病得到证实，易瑞沙应该停止，病人适当处理。
If interstitial lung disease is confirmed, it is suggested that it should stop, the patient should be appropriate treatment.
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