Gaeta M, Volta S, Barone M, Caruso R, Loria G, Pandolfo I, Minutoli A
Servizio di Diagnostica per Immagini, Ospedale Piemonte, USL 42, Messina.
Radiol Med. 1994 Apr;87(4):427-34.
Twenty-one CT examinations of 18 patients with a known bronchioloalveolar carcinoma in the lung were retrospectively reviewed to describe the CT features of bronchioloalveolar carcinomas. Surgical specimens were available in 13 cases in which CT-histologic correlation was also obtained. In 5 patients the diagnosis was made with cytology and confirmed with radiologic-clinical follow-up. Three patients were reexamined for relapses 6-20 months after the resection of a localized carcinoma. Carcinomas exhibited 3 radiologic patterns: a) solitary pulmonary nodule (11 cases), b) mass or pulmonary consolidation (3 cases) and c) multicentric or diffuse disease (7 cases). Solitary nodular bronchioloalveolar carcinomas were associated with irregular or spiculated margins in 9 of 11 patients. In some cases internal inhomogeneity due to bubble-like radiolucencies was demonstrated. At pathology, bubble-like radiolucencies correlated with air-containing cystic spaces lined by neoplastic epithelium or patent and dilated bronchi. Some nodules exhibited linear and serpentine internal radiolucencies. Pathology demonstrated them to be consistent with patent intratumoral bronchioles (air bronchiologram) and air-containing neoplastic glandular spaces, respectively. In two cases a perinodular ground-glass halo was demonstrated surrounding the nodule (CT halo sign), due to perinodular lepidic tumor growth. Massive or ground-glass opacity involving a pulmonary segment or a lobe was another CT pattern of bronchioloalveolar carcinoma. An air bronchogram was usually demonstrated within the lesion. In the mucinous type of bronchioloalveolar carcinoma, pulmonary consolidations had a low CT value because of the large amount of intratumoral mucus. The diffuse type of tumor presented as multiple pulmonary nodules or multiple pulmonary consolidations, or both. In two cases multiple nodules were associated with carcinomatous lymphangitis. In conclusion, bronchioloalveolar carcinoma should be considered in the differential diagnosis of solitary pulmonary nodules, multiple pulmonary nodules and chronic alveolar opacities. The diagnosis of a bronchioloalveolar carcinoma is of great value since surgery can help nearly 70% of the patients at this stage recover.
对18例已知肺细支气管肺泡癌患者的21次CT检查进行回顾性分析,以描述细支气管肺泡癌的CT特征。13例有手术标本,同时获得了CT与组织学的相关性。5例患者通过细胞学诊断,并经影像学 - 临床随访证实。3例患者在局限性癌切除术后6 - 20个月因复发接受复查。癌表现出3种影像学模式:a)孤立性肺结节(11例),b)肿块或肺实变(3例),c)多中心或弥漫性病变(7例)。11例孤立性结节状细支气管肺泡癌中,9例边缘不规则或有毛刺。部分病例显示因气泡样透亮区导致的内部不均匀性。病理检查时,气泡样透亮区与由肿瘤上皮衬里的含气囊性空间或开放和扩张的支气管相关。部分结节显示线性和蜿蜒状内部透亮区。病理显示它们分别与肿瘤内开放的细支气管(空气支气管造影)和含气的肿瘤性腺样空间一致。2例病例中结节周围显示有磨玻璃样晕(CT晕征),这是由于结节周围鳞屑样肿瘤生长所致。累及肺段或肺叶的大片状或磨玻璃样实变是细支气管肺泡癌的另一种CT模式。病变内通常可见空气支气管造影。在黏液型细支气管肺泡癌中,由于肿瘤内黏液量多,肺实变的CT值较低。弥漫型肿瘤表现为多发肺结节或多发肺实变,或两者皆有。2例病例中多发结节与癌性淋巴管炎相关。总之,在孤立性肺结节、多发肺结节和慢性肺泡性实变疾病的鉴别诊断中应考虑细支气管肺泡癌。细支气管肺泡癌的诊断具有重要价值,因为在此阶段手术可使近70%的患者康复。