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Children with congenital cystic adenomatoid malformation of the lung CT diagnosis

机译:小儿先天性囊性腺瘤样畸形的肺部CT诊断

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摘要

In this study, we aim to investigate the imaging appearances of congenital cystic adenomatoid malformation (CCAM) of the lung, and to enhance the understanding of this disease. A total of 11 cases with CCAM of the lung were confirmed by surgery and pathology. Preoperative chest computed tomography (CT) scan was performed in all patients, and high resolution CT scan was performed in lesion areas of 7 cases. Our results showed that there were 3 cases involving left and right lung, 5 cases involving right lung and 3 cases involving left lung. CT scan showed 6 cases with single or multiple air-filled cavities (> 2 cm in diameter) and 5 cases with multiple honeycomb-like cysts (< 1 cm in diameter). The cysts of CCAM contained air in 9 cases and a small amount of liquid in 2 cases. The complications of CCAM included different degree of emphysema in 7 patients, mediastinal hernia in 5 cases and congenital pulmonary sequestration in 1 case. All lesions have certain space-occupying effect. In conclusion, CT manifestation of CCAM of lung has certain characteristics and can provide reliable information for diagnosis of the disease.
机译:在这项研究中,我们旨在调查先天性肺囊性腺瘤样畸形(CCAM)的影像学表现,并增强对这种疾病的了解。通过手术和病理证实总共11例肺部CCAM。所有患者均进行术前胸部计算机断层扫描(CT)扫描,并在7例病变区域进行了高分辨率CT扫描。我们的结果显示,有3例涉及左右肺,5例涉及右肺,3例涉及左肺。 CT扫描显示6例有单个或多个充气腔(直径> 2厘米)和5例多个蜂窝状囊肿(直径<1厘米)。 CCAM的囊肿包含空气9例和少量液体2例。 CCAM的并发症包括不同程度的肺气肿7例,纵隔疝5例和先天性肺隔离症1例。所有病变均具有一定的占位作用。综上所述,肺部CCAM的CT表现具有一定的特征,可以为疾病的诊断提供可靠的信息。

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