Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan,
Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Respiration. 2019;97(4):319-328. doi: 10.1159/000494061. Epub 2018 Dec 6.
Idiopathic pleuroparenchymal fibroelastosis (IPPFE) is a rare interstitial pneumonia that is characterized by stiffness in both the upper lobes and pleura, which is evident on high resolution computed tomography (HRCT) of the chest. However, prognostic factors for IPPFE have not been identified yet.
We aimed to investigate the clinical prognostic factors affecting survival in patients with IPPFE.
Between April 2009 and September 2017, we enrolled 36 patients who were clinically diagnosed with IPPFE, using HRCT. These patients were classified as either short survival (dead within 12 months from the diagnosis of IPPFE) or long survival (survived for greater than 12 months) groups. We retrospectively analyzed the clinical characteristics, serum markers, pulmonary function test results, and HRCT findings.
Twelve patients were classified into the short survival and 24 were categorized into long survival categories. At the time of diagnosis, the incidence of coexistence of a usual interstitial pneumonia (UIP) pattern in the lower lobes on HRCT in the short survival was significantly higher than that in the long survival. Multivariate analysis revealed that a UIP pattern in the lower lobes on HRCT was the only independent variable for poor prognosis. The median survival time from diagnosis in patients with IPPFE was 24 months. Of these patients with IPPFE, the survival time with a UIP pattern was significantly shorter than in those without a UIP pattern.
Our findings suggest that a UIP pattern in the lower lobes at the time of diagnosis was an independent prognostic factor for IPPFE.
特发性胸膜肺弹力纤维增生症(IPPFE)是一种罕见的间质性肺炎,其特征是上叶和胸膜僵硬,胸部高分辨率计算机断层扫描(HRCT)可见。然而,IPPFE 的预后因素尚未确定。
我们旨在研究影响 IPPFE 患者生存的临床预后因素。
2009 年 4 月至 2017 年 9 月,我们纳入了 36 例经 HRCT 临床诊断为 IPPFE 的患者。这些患者分为短期存活(IPPFE 诊断后 12 个月内死亡)和长期存活(存活时间超过 12 个月)组。我们回顾性分析了临床特征、血清标志物、肺功能测试结果和 HRCT 发现。
12 例患者归入短期存活组,24 例归入长期存活组。在诊断时,短期存活组 HRCT 上存在下叶普通间质性肺炎(UIP)模式的发生率明显高于长期存活组。多变量分析显示,HRCT 上存在下叶 UIP 模式是预后不良的唯一独立变量。IPPFE 患者从诊断到中位生存时间为 24 个月。在这些 IPPFE 患者中,具有 UIP 模式的生存时间明显短于无 UIP 模式的生存时间。
我们的研究结果表明,诊断时存在下叶 UIP 模式是 IPPFE 的独立预后因素。