Liu Tongxi, Gao Li, Xie Sheng, Sun Hongliang, Liu Min, Zhai Zhenguo
Department of Radiology, China-Japan Friendship Hospital, Beijing, 100029, China.
Department of Radiology, Peking University First Hospital, Beijing, 100034, China.
Clin Respir J. 2018 May;12(5):1974-1980. doi: 10.1111/crj.12766. Epub 2018 Feb 9.
Fibrosing mediastinitis (FM) is a rare disorder characterized by an excessive fibrotic reaction within the mediastinum, which can result in compression of mediastinal structures. To investigate the clinical and imaging characteristics of TB-associated FM, patients with evidence of TB infection were retrospectively evaluated in this study.
A total of 33 patients with clinically diagnosed FM and evidence of TB infection were selected from the database of two institutional medical centers. Medical records were reviewed to evaluate the clinical disease spectrum, responses to therapy and imaging characteristics.
TB-associated FM showed distinctive infiltrative pattern on chest CT, such as bilateral involvement and hilar predominance. The majority of patients presented with nonspecific respiratory symptoms due to the compression of mediastinal broncho-vascular structures. Echocardiography discovered pulmonary hypertension to various degrees in 60% of patients. Although only a part of patients responded to medical therapy, they seldom showed deterioration during the follow-up.
TB-associated FM shows some specific imaging characteristics, reflecting immune-mediated fibrotic reaction secondary to TB infection. The insidious progression to mediastinal fibrosis after TB infection poses a challenge to the early diagnosis and results in subsequent respiratory dysfunction and pulmonary hypertension.
纤维性纵隔炎(FM)是一种罕见的疾病,其特征为纵隔内出现过度纤维化反应,可导致纵隔结构受压。为了研究结核相关FM的临床和影像学特征,本研究对有结核感染证据的患者进行了回顾性评估。
从两个机构医疗中心的数据库中选取了33例临床诊断为FM且有结核感染证据的患者。查阅病历以评估临床疾病谱、治疗反应和影像学特征。
结核相关FM在胸部CT上表现出独特的浸润模式,如双侧受累和肺门为主。大多数患者因纵隔支气管血管结构受压而出现非特异性呼吸道症状。超声心动图发现60%的患者有不同程度的肺动脉高压。虽然只有部分患者对药物治疗有反应,但在随访期间很少出现病情恶化。
结核相关FM表现出一些特定的影像学特征,反映了结核感染继发的免疫介导纤维化反应。结核感染后隐匿进展为纵隔纤维化对早期诊断构成挑战,并导致随后的呼吸功能障碍和肺动脉高压。