Hartman T E, Primack S L, Kang E Y, Swensen S J, Hansell D M, McGuinness G, Müller N L
Department of Diagnostic Radiology, Mayo Clinic, Rochester, MN 55905, USA.
Chest. 1996 Aug;110(2):378-82. doi: 10.1378/chest.110.2.378.
To determine the outcome of areas of ground-glass attenuation and assess disease progression on serial high-resolution CT (HRCT) scans of patients with biopsy specimen-proved usual interstitial pneumonia (UIP) and desquamative interstitial pneumonia (DIP).
Twelve patients with biopsy specimen-proved UIP and 11 patients with biopsy specimen-proved DIP who had initial and follow-up HRCT scans (median interval, 10 months) were reviewed. Eleven patients with UIP and 11 with DIP received treatment between the initial and follow-up CT scans. The scans were evaluated for the presence and extent of ground-glass attenuation, irregular linear opacities and honeycombing, and overall extent of parenchymal involvement.
On initial CT scans, all 12 patients with UIP had areas of ground-glass attenuation (mean +/- SD extent, 30 +/- 16%) and irregular lines (mean +/- SD extent, 17 +/- 7%) and 10 patients had honeycombing (mean +/- SD extent, 10 +/- 6%). All 11 patients with DIP had areas of ground-glass attenuation on initial HRCT scans (mean +/- SD extent, 51 +/- 26%), 5 patients had irregular linear opacities (mean +/- SD extent, 5 +/- 5%), and 1 patient had honeycombing. Nine of the 12 patients with UIP showed increase in the extent of ground-glass attenuation (n = 6) or progression to irregular lines (n = 2) or honeycombing (n = 4) on follow-up as compared with only 2 patients with DIP who showed progression to irregular lines (n = 1) or honeycombing (n = 1) (p < 0.01 chi 2 test).
In patients with UIP, areas of ground-glass attenuation usually increase in extent or progress to fibrosis despite treatment. Areas of ground-glass attenuation in most patients with DIP remain stable or improve with treatment.
通过对经活检证实为普通型间质性肺炎(UIP)和脱屑性间质性肺炎(DIP)患者的系列高分辨率CT(HRCT)扫描,确定磨玻璃影区域的转归并评估疾病进展情况。
回顾性分析12例经活检证实为UIP的患者以及11例经活检证实为DIP的患者,这些患者均有初始及随访HRCT扫描(中位间隔时间为10个月)。11例UIP患者和11例DIP患者在初始CT扫描和随访CT扫描之间接受了治疗。对扫描结果进行评估,观察磨玻璃影、不规则线状影和蜂窝状影的存在及范围,以及实质受累的总体范围。
在初始CT扫描时,所有12例UIP患者均有磨玻璃影区域(平均±标准差范围为30±16%)和不规则线状影(平均±标准差范围为17±7%),10例患者有蜂窝状影(平均±标准差范围为10±6%)。所有11例DIP患者在初始HRCT扫描时均有磨玻璃影区域(平均±标准差范围为51±26%),5例患者有不规则线状影(平均±标准差范围为5±5%),1例患者有蜂窝状影。与仅2例DIP患者出现进展至不规则线状影(1例)或蜂窝状影(1例)相比,12例UIP患者中有9例在随访时磨玻璃影区域范围增大(6例)或进展为不规则线状影(2例)或蜂窝状影(4例)(χ²检验,p<0.01)。
在UIP患者中,尽管接受了治疗,磨玻璃影区域通常范围会增大或进展为纤维化。大多数DIP患者的磨玻璃影区域保持稳定或经治疗后改善。