Zavaletta VA, Bartholmai BJ, Robb RA: High resolution multidetector CT-aided tissue analysis and quantification of lung fibrosis. Acad Radiol 14(7):772–787, 2007 CentralZavaletta VA, Bartholmai BJ, Robb RA. High resolution multidetector CT-aided tissue analysis and quantification of lung ...
Although increasing used in the preclinical testing of new anti-fibrotic drugs, a thorough validation of micro-computed tomography (CT) in pulmonary fibrosis models has not been performed. Moreover, no attempts have been made so far to define density thresholds to discriminate between aeration levels...
No clinical study has compared lung or lobe volumes on computed tomography (CT) between the supine and standing positions in patients with idiopathic lung fibrosis (IPF). This study aimed to compare lung and lobe volumes between the supine and standing positions and evaluate the correlations betwee...
Application of lung biopsy in diagnosis of idiopathic pulmonary fibrosis HAN Qian, LUO Qun State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, the First Affiliated Hospital of Guangzhou Medical University, Guangdong...
PURPOSE: To compare a computed tomographic (CT)-based scoring system with nonimaging indexes of pulmonary status in patients with cystic fibrosis. MATERIALS AND METHODS: Pulmonary CT findings were assessed in 117 patients with cystic fibrosis, with cases classified according to three groups by age; ...
46Sarcoidosis: fibrosis with traction bronchiectasis. 47. Sarcoidosis: peribronchovascular fibrosis with traction bronchiectasis, mild honeycombing 48Sarcoidosis: traction bronchiectasis and cysts. 49. 50. Sarcoidosis: fibrosis with cysts 51. Sarcoidosis: traction bronchiectasis, cysts, emphysema, aspergilloma...
特发性间质性纤维化idiopathicpulmonaryfibrosis(IPF)的患者典型的伴蜂窝改变honeycombing和牵拉性支气管扩张的寻常型间质性肺炎.HRCT上分布极为重要多数病例小结节的分布可分成三类:淋巴周围型,小叶中央型和随机型.淋巴周围型分布Perilymphaticdistribution结节见于与胸膜面,小叶间隔和气管血管周围间质相关的部位,胸膜下几乎...
Evolution of CT findings in patients with cystic fibrosis. The aim of our study was to assess the evolution of pulmonary CT findings in cystic fibrosis patients. Serial CT examinations were performed in four differ... TH Helbich,G Heinz-Peer,D Fleischmann,... - 《Ajr American Journal of Roe...
Ultrasound B-lines in the evaluation of interstitial lung disease in patients with systemic sclerosis: cut-off point definition for the presence of significant pulmonary fibrosis. Medicine (Baltimore). 2018;97(18):e0566. Article Google Scholar Liu J, Wang Y, Fu W, Yang CS, Huang JJ. ...
Pulmonary fibrosis, characterized by excessive collagen deposition in the lungs, comprises a key and debilitating component of chronic lung diseases. Methods are lacking for the direct visualization of fibrillar collagen throughout the whole murine lung,