急性嗜酸性粒细胞肺炎导致特发性肺纤维化急性加重。

HCA healthcare journal of medicine Pub Date : 2025-02-01 eCollection Date: 2025-01-01 DOI:10.36518/2689-0216.1802
Duncan A McKinney, Noah R Kosnik, Shahzeib Syed, Gretchen Junko
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摘要

特发性肺纤维化(IPF)是一种进行性疾病,其特征是肺实质逐渐被纤维组织破坏和取代,并伴有慢性炎症。它通常被认为是一种典型的间质性肺疾病,在该家族中是最普遍的,也许也是最危险的。虽然这种疾病在一般人群中并不常见,但其患病率随着年龄的增长而增加,通常在65岁左右被诊断出来。这并不排除IPF在年轻个体中的发展,无论年龄大小,诊断后的平均生存期为2至5年。当代研究已经深入了解了肺实质改变如何导致对机会性感染的易感性增加。也有研究表明,引起炎症的肺部损伤,如肺炎,可能会加速IPF的进展。嗜酸性粒细胞肺炎是一系列肺部疾病,其中嗜酸性粒细胞介导的炎症导致呼吸系统损伤。早期识别和适当的干预对于将残余肺功能缺陷的风险降至最低至关重要,这种风险在具有单独肺危险因素的个体中会增加。虽然及时诊断和药物干预与改善预后相关,但IPF患者仍有恶化到需要肺移植的风险。对那些有风险的人进行早期筛查仍然是一个有趣的话题。尽管IPF普遍存在,但其发病机制仍然知之甚少,并且很少有可用的治疗方案。在这篇文章中,我们记录了一个独特的病例,以前未确诊的IPF在一个年轻人的急性嗜酸性粒细胞性肺炎和机会性生物,黑曲霉的参与下急剧恶化。病例部分将作为一个过渡,讨论每个主要的病理因素在发挥作用,支持最近的文献回顾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute Exacerbation of Idiopathic Pulmonary Fibrosis in the Setting of Acute Eosinophilic Pneumonia.

Description Idiopathic pulmonary fibrosis (IPF) is a progressive disease characterized by gradual destruction and replacement of pulmonary parenchyma with fibrous tissue, which occurs in conjunction with chronic inflammation. It is often considered a prototypical interstitial lung disease and is both the most prevalent and perhaps the most dangerous in that family. Although the disease is uncommon in the general population, its prevalence increases with age and is typically diagnosed around the age of 65. This does not preclude the development of IPF in younger individuals, and the mean survival is 2 to 5 years post-diagnosis regardless of age. Contemporary studies have provided insight into how altered pulmonary parenchyma results in increased susceptibility to opportunistic infections. It has also been demonstrated that pulmonary insults that cause inflammation, such as pneumonia, may accelerate the progression of IPF. Eosinophilic pneumonias are a collection of pulmonary diseases in which eosinophil-mediated inflammation results in respiratory compromise. Early recognition and appropriate intervention are imperative to minimize the risk of residual pulmonary function deficits, a risk that is increased in individuals with separate pulmonary risk factors. While prompt diagnosis and pharmacologic interventions are associated with improved outcomes, patients with IPF remain at risk of deterioration to the point of requiring lung transplantation. Early screening for those at risk continues to be a topic of interest. Despite the prevalence of IPF, its pathogenesis remains poorly understood and few management options are available. In this article, we document a unique case of previously undiagnosed IPF in a young individual that acutely worsened in the setting of acute eosinophilic pneumonia and the involvement of an opportunistic organism, Aspergillus niger. The case section will serve as a transition into a discussion of each of the major pathologic factors at play, supported by a review of recent literature.

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