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伴纤维化的非特异性间质性肺炎:高分辨率CT及病理表现

Nonspecific interstitial pneumonia with fibrosis: high-resolution CT and pathologic findings.

作者信息

Kim T S, Lee K S, Chung M P, Han J, Park J S, Hwang J H, Kwon O J, Rhee C H

机构信息

Department of Radiology, College of Medicine, Samsung Medical Center, Sungkyunkwan University, Seoul, Korea.

出版信息

AJR Am J Roentgenol. 1998 Dec;171(6):1645-50. doi: 10.2214/ajr.171.6.9843306.

DOI:10.2214/ajr.171.6.9843306
PMID:9843306
Abstract

OBJECTIVE

The purpose of our study was to describe high-resolution CT findings of nonspecific interstitial pneumonia with fibrosis and to compare findings seen on CT with pathologic findings.

MATERIALS AND METHODS

High-resolution CT findings of biopsy-proven non-specific interstitial pneumonia with fibrosis from 23 consecutive patients (one man and 22 women) were analyzed retrospectively by two chest radiologists. CT findings were compared with pathologic findings.

RESULTS

The predominant high-resolution CT finding, seen in all patients, was bilateral patchy areas of ground-glass opacity with (35%) or without (65%) areas of consolidation. Irregular linear opacities (87%), thickening of bronchovascular bundles (65%), and bronchial dilatation (52%) were also frequently seen. Honeycombing was not seen in any patient. All parenchymal abnormalities showed subpleural predominance. Areas of ground-glass opacity with or without irregular linear opacity or bronchial dilatation on CT corresponded pathologically to areas of interstitial thickening caused by varying degrees of interstitial inflammation and fibrosis showing temporal uniformity. Areas of consolidation, seen at five biopsy sites, represented the areas of bronchiolitis obliterans organizing pneumonia, foamy cell collections in alveolar spaces, or microscopic honeycombing with mucin stasis.

CONCLUSION

On high-resolution CT, nonspecific interstitial pneumonia with fibrosis is most commonly revealed as patchy subpleural areas of ground-glass opacity mixed with irregular linear opacity or bronchial dilatation. These areas represent interstitial thickening caused by varying degrees of interstitial inflammation, fibrosis, or both.

摘要

目的

我们研究的目的是描述纤维化性非特异性间质性肺炎的高分辨率CT表现,并将CT表现与病理结果进行比较。

材料与方法

两名胸部放射科医生对23例经活检证实的纤维化性非特异性间质性肺炎患者(1名男性和22名女性)的高分辨率CT表现进行回顾性分析。将CT表现与病理结果进行比较。

结果

所有患者中最主要的高分辨率CT表现为双侧斑片状磨玻璃影,伴有(35%)或不伴有(65%)实变区。不规则线状影(87%)、支气管血管束增粗(65%)和支气管扩张(52%)也较为常见。所有患者均未见蜂窝状改变。所有实质异常均以胸膜下为主。CT上有或无不规则线状影或支气管扩张的磨玻璃影区域,病理上对应于不同程度的间质性炎症和纤维化导致的间质增厚区域,表现为时间上的一致性。在五个活检部位见到的实变区,代表闭塞性细支气管炎机化性肺炎、肺泡腔内泡沫细胞聚集或伴有黏液淤滞的显微镜下蜂窝状改变区域。

结论

在高分辨率CT上,纤维化性非特异性间质性肺炎最常见的表现为胸膜下斑片状磨玻璃影,伴有不规则线状影或支气管扩张。这些区域代表由不同程度的间质性炎症、纤维化或两者共同导致的间质增厚。

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