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非特异性间质性肺炎和特发性肺纤维化:疾病模式和分布随时间的变化

Nonspecific interstitial pneumonia and idiopathic pulmonary fibrosis: changes in pattern and distribution of disease over time.

作者信息

Silva C Isabela S, Müller Nestor L, Hansell David M, Lee Kyung S, Nicholson Andrew G, Wells Athol U

机构信息

Department of Radiology, Vancouver General Hospital, University of British Columbia, 3350-950 W 10th Ave, Vancouver, BC, Canada V5Z 4E3.

出版信息

Radiology. 2008 Apr;247(1):251-9. doi: 10.1148/radiol.2471070369. Epub 2008 Feb 12.

DOI:10.1148/radiol.2471070369
PMID:18270375
Abstract

PURPOSE

To retrospectively assess the change in disease pattern of nonspecific interstitial pneumonia (NSIP) and idiopathic pulmonary fibrosis (IPF) findings seen at thin-section computed tomography (CT) at long-term follow-up and to compare the same with initial findings at CT.

MATERIALS AND METHODS

The study included 48 patients (28 men, 20 women; mean age, 57.5 years) with biopsy-proved NSIP (n = 23) or IPF (n = 25) who underwent CT at initial diagnosis and at follow-up 34-155 months later. The CT scans were randomized and reviewed by two independent thoracic radiologists for pattern and distribution of ground-glass opacity (GGO), reticulation, traction bronchiectasis and bronchiolectasis, and honeycombing. Statistical analysis was performed by using nonparametric methods and univariate logistic regression.

RESULTS

Follow-up CT in patients with NSIP showed marked decrease in the extent of GGO, increase in reticulation, and a greater likelihood of peripheral distribution (all P < .05). At presentation, the CT findings were interpreted as suggestive of NSIP in 18 of 23 patients with NSIP and indeterminate or suggestive of IPF in five. In five (28%) of 18 patients with initial findings suggestive of NSIP, the follow-up CT scans were interpreted as more suggestive of IPF. No CT features seen at presentation allowed distinction between patients with NSIP that maintained an NSIP pattern at follow-up and those that progressed to an IPF pattern.

CONCLUSION

At follow-up CT, 28% of patients with initial CT findings suggestive of NSIP progressed to findings suggestive of IPF. Similar initial CT findings for NSIP may have different imaging outcomes.

摘要

目的

回顾性评估非特异性间质性肺炎(NSIP)和特发性肺纤维化(IPF)在薄层计算机断层扫描(CT)上的疾病模式变化,并将其与CT初始表现进行比较。

材料与方法

本研究纳入48例患者(28例男性,20例女性;平均年龄57.5岁),经活检证实为NSIP(n = 23)或IPF(n = 25),这些患者在初始诊断时及34 - 155个月后的随访时均接受了CT检查。CT扫描结果随机分组,由两名独立的胸放射科医生进行评估,观察磨玻璃影(GGO)、网状影、牵拉性支气管扩张和细支气管扩张以及蜂窝状影的模式和分布。采用非参数方法和单因素逻辑回归进行统计分析。

结果

NSIP患者的随访CT显示GGO范围明显减小,网状影增加,且外周分布的可能性更大(均P <.05)。初诊时,23例NSIP患者中有18例的CT表现提示为NSIP,5例为不确定或提示为IPF。在18例初诊表现提示为NSIP的患者中,有5例(28%)的随访CT扫描结果更提示为IPF。初诊时所见的CT特征无法区分随访时维持NSIP模式的NSIP患者和进展为IPF模式的患者。

结论

在随访CT中,28%初诊CT表现提示为NSIP的患者进展为提示IPF的表现。NSIP相似的初始CT表现可能有不同的影像学结果。

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