病例系列:两名患者的间歇性肺病与IPF模式呈现自发性肺胸部-临床过程
Amit Toshniwal1, Babaji Ghewade1, Alushika Jain1
1Datta Meghe Institute of Medical Sciences, Wardha, India.
Frontiers in medicine
|October 31, 2025
概括
间歇性肺病 (ILD) 可能导致罕见的并发症,如肺胸炎,肺中炎和皮下肺. 这一案例系列强调了急需在ILD患者中迅速识别和管理这些严重疾病的关键需求.
科学领域:
- 肺部病理学 肺部病理学
- 内部医学 内部医学
- 放射学 放射学是一门学科.
背景情况:
- 间歇性肺部疾病 (ILD) 是一组纤维化的肺部疾病.
- 肺胸炎是已知的纤维性ILD的并发症.
- 肺胸,肺中和皮下肺的三位一体在ILD中异常罕见.
研究的目的:
- 介绍一个两名ILD患者的病例系列,他们经历了自发性肺胸.
- 要突出在纤维性ILD中罕见的肺胸部,肺中和皮下肺气同时发生的情况.
- 强调识别和管理这些并发症的重要性.
主要方法:
- 案例系列方法.
- 对两名被诊断患有异常性肺纤维化 (IPF) - ILD.模式的患者进行了审查.
- 对成像发现和临床结果的分析.
主要成果:
- 一名患者出现了自发性肺胸部,肺中和皮下肺,因呼吸衰竭而死亡.
- 第二个患有可能常见间歇性肺炎 (UIP) - ILD模式的患者成功地保守地控制了自发性肺胸部.
- 本系列是第一个报告纤维性ILD中皮下肺气,肺中和肺胸三重体的系列.
结论:
- 肺胸,肺中和皮下肺同时发生是一种罕见但严重的纤维性ILD并发症.
- 及时识别和多学科管理对于高风险的ILD患者至关重要.
- 这一案例系列有助于了解罕见的ILD并发症.
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