Cozzi Diletta, Bargagli Elena, Calabrò Alessandro Giuseppe, Torricelli Elena, Giannelli Federico, Cavigli Edoardo, Miele Vittorio
Department of Radiology, Careggi University Hospital, L.go Giovanni Alessandro Brambilla, 3, 50134, Florence, Italy.
Section of Respiratory Medicine, Department of Clinical and Experimental Biomedical Sciences, AOUC, Florence, Italy.
Radiol Med. 2018 Mar;123(3):174-184. doi: 10.1007/s11547-017-0830-y. Epub 2017 Nov 9.
To present our experience of cases of pulmonary sarcoidosis with atypical HRCT patterns found during 2016 focusing on the differential diagnosis to contribute to the difficult role of the radiologist in the disease identification and to help the clinicians to reach the diagnosis.
The HRCT examinations of 47 patients with sarcoidosis were studied retrospectively. All patients had a histopathological confirm of the disease. 29 (61.7%) show a typical pulmonary pattern and 18 (38.3%) an atypical pattern. The latter were evaluated by three experienced radiologists dedicated to thoracic disease to radiologically define the predominant pattern of presentation.
In the 18 patients (38.3%) with atypical sarcoidosis, the following parenchymal patterns were observed: four patients (22.2%) had interstitial fibrotic alterations, three patients (16.6%) with reticular pattern with inter-intralobular septal thickening, two patients (11.1%) with small-airway involvement with mosaic oligoemia, two patients (11.1%) with pleural involvement (pneumothorax and pleural plaques), one patient (5.5%) with fibrocystic changes, 1 (5.5%) with halo-sign, 1 (5.5%) with diffuse bilateral ground-glass opacities, and 1 (5.5%) with isolated lung mass; in addition, three patients (16.6%) with atypical lymph node pattern were also found.
The atypical pulmonary alterations found in CT examination can be confused with other lung diseases and they are always a challenge even for the most experienced radiologist. In our experience, cases with atypical pulmonary sarcoidosis patterns evaluated in the study are consistent with similar cases described in the literature, both in lymph node and atypical parenchymal involvement. All the atypical characteristics of the work should alert the radiologist to consider sarcoidosis among the possible differential diagnoses, always correlating the results of the computed tomography examination with appropriate clinical-laboratory evaluations.
介绍我们在2016年期间发现的具有非典型高分辨率计算机断层扫描(HRCT)表现的肺结节病病例的经验,重点在于鉴别诊断,以协助放射科医生在疾病识别中发挥困难的作用,并帮助临床医生做出诊断。
回顾性研究47例结节病患者的HRCT检查。所有患者均经组织病理学确诊。29例(61.7%)表现为典型的肺部影像,18例(38.3%)表现为非典型影像。后者由三位专注于胸部疾病的经验丰富的放射科医生进行评估,以从影像学上确定主要的表现形式。
在18例(38.3%)非典型结节病患者中,观察到以下肺实质影像表现:4例(22.2%)有间质纤维化改变,3例(16.6%)为伴有小叶间隔增厚的网状影像,2例(11.1%)有小气道受累伴马赛克样低灌注,2例(11.1%)有胸膜受累(气胸和胸膜斑),1例(5.5%)有纤维囊性改变,1例(5.5%)有晕征,1例(5.5%)有弥漫性双侧磨玻璃影,1例(5.5%)有孤立性肺肿块;此外,还发现3例(16.6%)有非典型淋巴结影像。
CT检查中发现的非典型肺部改变可能与其他肺部疾病混淆,即使对经验最丰富的放射科医生来说也是一项挑战。根据我们的经验,本研究中评估的非典型肺结节病病例在淋巴结和非典型肺实质受累方面与文献中描述的类似病例一致。所有这些非典型特征应提醒放射科医生在可能的鉴别诊断中考虑结节病,始终将计算机断层扫描检查结果与适当的临床实验室评估结果相关联。