结节病患者高分辨率计算机断层扫描的纤维化改变。

Marek Pasławski, Witold Krupski, Janusz Złomaniec
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引用次数: 0

摘要

本研究的目的是在结节病患者的高分辨率计算机断层扫描中呈现典型的纤维化变化。材料包括18例结节病患者,其中进行了HRCT检查。扫描从肺尖到横膈膜水平,在充分吸气时,患者仰卧位。记录并分析HRCT表现的存在和特征。进行额外的呼气扫描以诊断空气潴留,如果胸膜下密度在后部,依赖肺部区域,则在俯卧位患者中进行额外的扫描。5例患者在融合结节病变区发现纤维化改变。纤维化区可见支气管扩张、实质带和纤维化团块。6例患者以网状病变为主。增厚的小叶间隔在疾病缓解期间没有消退,提示存在不可逆的网状纤维化改变。严重纤维化导致肺实质破坏,伴大面积肺蜂窝。在活动性病变区纤维化改变伴牵引性支气管扩张伴合并结节改变和实变。活动性可逆性改变消退后,5例患者出现密集纤维化伴大支气管扩张,形成网状网状的蜂窝状改变。在三个病例中,最强烈的纤维化和生产性(肉芽肿)变化局限于下肺叶,模拟特发性肺纤维化。结节病的典型HRCT表现是众所周知的。但大多数结节、磨玻璃混浊、支气管血管周围增厚或肺门腺病变是可逆的。大约25%的患者出现不可逆的纤维化改变。在早期阶段,它们在x线平片上甚至在正常的CT切片上都是微妙和不可见的。因此,HRCT对结节病患者的纤维化变化和监测疾病的进展是必要的。因此,了解纤维化的HRCT征象至关重要。
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Fibrotic changes in high-resolution computed tomography in patients with sarcoidosis.

The aim of the study is presenting the typical findings of fibrotic changes in high-resolution computed tomography in patients with sarcoidosis. Material comprises a group of 18 patients with sarcoidosis, in whom HRCT examination was performed. The scanning was performed from lung apices to the level of diaphragm, at full inspiration with patients in supine position. The presence and character of HRCT findings were noted and analyzed. Additional expiratory scans were performed to diagnose air-trapping, and in case of subpleural densities in posterior, dependent lung areas additional scans were obtaining in prone patients positions. Fibrotic changes were found in the area of confluent nodular lesions in five patients. In these fibrotic areas the bronchiectasis, as well as parenchymal bands and fibrotic masses were seen. In six patients the reticular pattern was the predominant pathology. Thickened lobular septa did not resolve during the remission of the diseases, suggesting the presence of irreversible, reticular fibrotic changes. Intensive fibrosis led towards destruction of the lung parenchyma, with honeycombing involving large lung areas. In the areas of active disease fibrotic changes with traction bronchiectasis were accompanied by the confluent nodular changes and presence of consolidation. After resolving of active reversible changes the intensive fibrosis with large bronchiectasis forming the honeycombing pattern with reticular changes were seen in five patients. In three cases the most intensive changes both fibrotic and productive (granuloma) changes were localized in the lower lobe, mimicking the idiopathic pulmonary fibrosis. The classical HRCT findings in sarcoidosis are well known. But most of them, nodules, ground glass opacities, peribronchovascular thickening or hilar adenopathy are reversible. The irreversible fibrotic changes develop in about 25% of patients. In the early stage they are subtle and invisible on plain radiographs or even on normal CT sections. So the HRCT is necessary to reveal fibrotic changes in patients with sarcoidosis and to monitor the progression of the diseases. Therefore, the good knowledge of HRCT signs of fibrosis is essential.

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