Su Ruihua, Wen Yanhua, Liufu Yuling, Pan Xiaohuan, Guan Yubao
From the Department of Radiology, the Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou.
Department of Radiology, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
J Comput Assist Tomogr. 2023;47(3):418-423. doi: 10.1097/RCT.0000000000001439. Epub 2023 Mar 3.
Our study aimed to elucidate the computed tomography (CT) features and follow-up course of pulmonary nocardiosis patients to improve the understanding and diagnostic accuracy of this disease.
The chest CT findings and clinical data of patients diagnosed with pulmonary nocardiosis by culture or histopathological examination in our hospital between 2010 and 2019 were retrospectively analyzed.
A total of 34 cases of pulmonary nocardiosis were included in our study. Thirteen patients were on long-term immunosuppressant therapy, among whom 6 had disseminated nocardiosis. Among the immunocompetent patients, 16 had chronic lung diseases or a history of trauma. Multiple or solitary nodules represented the most common CT feature (n = 32, 94.12%), followed by ground-glass opacities (n = 26, 76.47%), patchy consolidations (n = 25, 73.53%), cavitations (n = 18, 52.94%), and masses (n = 11, 32.35%). There were 20 cases (61.76%) with mediastinal and hilar lymphadenopathy, 18 (52.94%) with pleural thickening, 15 (44.12%) with bronchiectasis, and 13 (38.24%) with pleural effusion. Significantly higher rates of cavitations were observed among immunosuppressed patients (85% vs 29%, P = 0.005). At follow-up, 28 patients (82.35%) clinically improved with treatment, while 5 (14.71%) had disease progression, and 1 (2.94%) died.
Chronic structural lung diseases and long-term immunosuppressant use were found as risk factors for pulmonary nocardiosis. While the CT manifestations were highly heterogeneous, clinical suspicion should be raised upon findings of coexisting nodules, patchy consolidations, and cavitations, particularly in the presence of extrapulmonary infections such as those of the brain and subcutaneous tissues. A significant incidence of cavitations may be observed among immunosuppressed patients.
本研究旨在阐明肺诺卡菌病患者的计算机断层扫描(CT)特征及随访过程,以提高对该病的认识和诊断准确性。
回顾性分析2010年至2019年期间在我院通过培养或组织病理学检查确诊为肺诺卡菌病患者的胸部CT表现及临床资料。
本研究共纳入34例肺诺卡菌病患者。13例患者接受长期免疫抑制治疗,其中6例发生播散性诺卡菌病。在免疫功能正常的患者中,16例有慢性肺部疾病或外伤史。多发或单发结节是最常见的CT表现(n = 32,94.12%),其次是磨玻璃影(n = 26,76.47%)、斑片状实变(n = 25,73.53%)、空洞形成(n = 18,52.94%)和肿块(n = 11,32.35%)。20例(61.76%)有纵隔和肺门淋巴结肿大,18例(52.94%)有胸膜增厚,15例(44.12%)有支气管扩张,13例(38.24%)有胸腔积液。免疫抑制患者的空洞形成率显著更高(85%对29%,P = 0.005)。随访时,28例患者(82.35%)经治疗后临床症状改善,5例(14.71%)病情进展,1例(2.94%)死亡。
慢性结构性肺部疾病和长期使用免疫抑制剂是肺诺卡菌病的危险因素。虽然CT表现高度异质性,但当发现存在结节、斑片状实变和空洞形成,特别是伴有脑和皮下组织等肺外感染时,应提高临床怀疑。免疫抑制患者中可能观察到较高的空洞形成发生率。