Oppenheim C, Mamou-Mani T, Sayegh N, de Blic J, Scheinmann P, Lallemand D
Department of Pediatric Radiology, Hôpital des Enfants Malades, Paris, France.
AJR Am J Roentgenol. 1994 Jul;163(1):169-72. doi: 10.2214/ajr.163.1.8010206.
Pulmonary dysfunction is common in children who survive bronchopulmonary dysplasia. Chest radiographs are not satisfactory for the identification of the sequelae of bronchopulmonary dysplasia because, although they often show abnormalities, the abnormalities are usually minor and sometimes absent. We therefore assessed the value of CT for identifying the sequelae of bronchopulmonary dysplasia.
Twenty-three children (mean age, 4 years) who had survived neonatal bronchopulmonary dysplasia and had signs of chronic pulmonary dysfunction (recurrent episodes of coughing, wheezing, dyspnea, pneumonia, respiratory insufficiency) were examined with chest radiographs and high-resolution CT scans of the chest. Two reviewers qualitatively analyzed the chest radiographic and CT findings by describing the most consistently found lesions and their frequencies.
The chest radiographs showed hyperexpansion in 17, hyperlucent areas in 11, and linear opacities in 10 of the 23 children. Pleural thickening was not observed, and four children had normal findings on chest radiographs. All 23 CT scans showed abnormalities, including multifocal areas of hyperaeration, well-defined linear opacities, and triangular subpleural opacities with an external base and an internal apex. In 20 of 23 children, all three abnormalities were present. For the three other children, two of these three abnormalities were found. No bronchiectasis was observed in any of the cases.
Lesions in survivors of bronchopulmonary dysplasia with chronic pulmonary dysfunction are visualized better on CT scans than on chest radiographs. Importantly, CT findings of multifocal areas of hyperaeration, numerous linear opacities facing triangular subpleural opacities visible on several consecutive sections, and no bronchiectasis should suggest the presence of sequelae of bronchopulmonary dysplasia.
肺功能障碍在支气管肺发育不良存活儿童中很常见。胸部X线片对于支气管肺发育不良后遗症的识别并不令人满意,因为尽管它们常常显示异常,但这些异常通常较轻微,有时甚至不存在。因此,我们评估了CT在识别支气管肺发育不良后遗症方面的价值。
对23例(平均年龄4岁)存活的新生儿支气管肺发育不良且有慢性肺功能障碍体征(反复咳嗽、喘息、呼吸困难、肺炎、呼吸功能不全)的儿童进行了胸部X线片和胸部高分辨率CT扫描检查。两名阅片者通过描述最常见的病变及其频率对胸部X线片和CT表现进行了定性分析。
23例儿童中,胸部X线片显示17例有肺过度膨胀,11例有透亮区,10例有线状阴影。未观察到胸膜增厚,4例儿童胸部X线片表现正常。所有23例CT扫描均显示异常,包括多灶性肺气肿区域、边界清晰的线状阴影以及基底位于外侧、尖端位于内侧的三角形胸膜下阴影。23例儿童中有20例存在上述三种异常。另外3例儿童中,发现了这三种异常中的两种。所有病例均未观察到支气管扩张。
对于有慢性肺功能障碍的支气管肺发育不良存活者,CT扫描比胸部X线片能更好地显示病变。重要的是,CT表现为多灶性肺气肿区域、在连续多个层面可见众多朝向三角形胸膜下阴影的线状阴影且无支气管扩张,提示存在支气管肺发育不良后遗症。