idiopathic pulmonary fibrosis的意思|示意
[医]特发性肺纤维变性，特发性肺纤维化
idiopathic pulmonary fibrosis的用法详解
idiopathic pulmonary fibrosis的用法讲解
idiopathic pulmonary fibrosis是一种肺部疾病，通常被缩写为IPF。这种疾病是由于肺泡中的血管和支气管周围的纤维化组织增生导致的。虽然该病的主要原因未知，但医学界普遍认为它是身体自身免疫系统的一种反应。
idiopathic pulmonary fibrosis在英语中的用法非常普遍，尤其是在医学界和医学文献中。以下是一些常见的用法：
- Patients with idiopathic pulmonary fibrosis need careful monitoring and management.
- The prognosis for patients with idiopathic pulmonary fibrosis is generally poor.
- Recent advances in the treatment of idiopathic pulmonary fibrosis have shown promising results.
- Researchers continue to study the mechanisms behind idiopathic pulmonary fibrosis to improve treatment options.
总之，idiopathic pulmonary fibrosis是一种严重的肺部疾病，英语中的用法广泛。对于那些涉及医学或健康领域的人来说，了解这个术语的含义和用法是非常重要的。
idiopathic pulmonary fibrosis相关短语
1、 idiopathic pulmonary fibrosis IPF 特发性肺纤维化,特发性肺间质纤维化
2、 IPF Idiopathic pulmonary fibrosis 特发性肺纤维化
3、 Diffuse idiopathic pulmonary fibrosis 弥漫性特发性肺纤维化
4、 idiopathic pulmonary interstitial fibrosis 特发性肺间质纤维化,特发性间质性肺炎
5、 senile idiopathic pulmonary interstitial fibrosis 老年人特发性肺纤维化
6、 idiopathic pulmonary upper lobe fibrosis 特发性肺上叶纤维化
7、 idiopathic pulmonary interstital fibrosis 特发性肺间质纤维化
8、 idiopathic interstitial pulmonary fibrosis 特发性肺纤维化
idiopathic pulmonary fibrosis相关例句
These morphologic changes provide basis for formation of idiopathic pulmonary fibrosis.
上述形态学改变对特发性肺纤维化的形成提供了一些依据.
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Background Bloemycin ( BLM ) induced pulmonary fibrosis ( BPF ) is most widely used animal model for idiopathic pulmonary fibrosis.
博莱霉素 ( BLM ) 所致的肺纤维化 ( BPF ) 模型是最常用的研究特发性肺纤维化的动物模型.
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Objective To observe ultrastructural changes and study the pathogenesis of idiopathic pulmonary fibrosis.
目的观察特发性肺纤维化的超微结构变化并探讨其发病机理.
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Abstract: Objective To observe ultrastructural changes and study the pathogenesis of idiopathic pulmonary fibrosis.
文摘: 目的观察特发性肺纤维化的超微结构变化并探讨其发病机理.
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Idiopathic pulmonary fibrosis prognosis? Specific we look at.
特发性肺纤维化预后怎么样？具体的我们来看下。
Idiopathic pulmonary fibrosis ( IPF ) has a poor prognosis and a course that is unpredictable.
特 发性 肺纤维化预后不佳,其发展过程无法预知.
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Conclusions Mutations in the genes encoding telomerase components can appear as familial idiopathic pulmonary fibrosis.
结论:端粒酶组分的编码基因发生突变时,能以家庭性特发性肺纤维变性的形式出现.
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The most likely diagnosis is Idiopathic pulmonary fibrosis (IPF).
最可能的诊断是特发性肺纤维化（IPF）。