晕征
医学
病理
放射科
淋巴瘤
肺炎
淋巴系统
肺
病态的
粘膜相关淋巴组织
马尔特淋巴瘤
计算机断层摄影术
内科学
作者
Wenhua Bi,Shuo Zhao,Chongchong Wu,Jie Gao,Suping Zhao,Shifeng Yang,Yan Deng,Pei Nie,Xinxin Yu,Hui Deng,Xuelei Zang,Xidong Ma,Jun Han,Idorenyin Polycarp Asuquo,Ximing Wang,Xinying Xue
摘要
Abstract Background Pulmonary mucosa‐associated lymphoid tissue lymphoma (MALToma) is the most frequent subset of primary pulmonary lymphoma. This study aimed to identify radiologic characteristics of pulmonary MALToma based on computed tomography (CT) observations and pathologic features, and further investigate its prognosis. Methods Sixty‐six patients (55.4 ± 10.9 years; 51.5% male) diagnosed as pulmonary MALToma by pathology were retrospectively enrolled. According to distributions and features of lesions shown on CT, patients were divided into three patterns, including single nodular/mass, multiple nodular/mass, and pneumonia‐like consolidative. Results Variety of the location and extent of the lymphomatous infiltration accounted for different characteristics demonstrated at CT. The pneumonia‐like consolidative pattern was the most frequent pattern observed in 42 patients (63.6%), followed by single nodular/mass (21.2%) and multiple nodular/mass (15.2%). CT features included air bronchogram (72.7%), well‐marginated halo sign (53.0%), coarse spiculate with different lengths (72.7%), angiogram sign (77.1% of 35 patients), peribronchovascular thickening (48.5%), irregular cavitation (16.7%) and pulmonary cyst (7.6%). The estimated 5‐year cumulative overall survival rate of pulmonary MALToma was 100.0%. Conclusions Pulmonary MALToma demonstrates several characteristics at CT. Identification of the significant pulmonary abnormalities of this indolent disease entity might be helpful for early diagnosis and optimal treatment.
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