USUAL INTERSTITIAL PNEUMONIA - HISTOLOGIC CORRELATION WITH HIGH-RESOLUTION CT

被引:208
作者
NISHIMURA, K [1 ]
KITAICHI, M [1 ]
IZUMI, T [1 ]
NAGAI, S [1 ]
KANAOKA, M [1 ]
ITOH, H [1 ]
机构
[1] KYOTO UNIV HOSP, DEPT RADIOL & NUCL MED, KYOTO 606, JAPAN
关键词
COMPUTED TOMOGRAPHY (CT); HIGH-RESOLUTION; LUNG; CT; FIBROSIS; PNEUMONITIS; USUAL INTERSTITIAL;
D O I
10.1148/radiology.182.2.1732946
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
The authors reviewed 46 cases of idiopathic pulmonary fibrosis with usual interstitial pneumonia (UIP), correlating findings on high-resolution computed tomographic (HRCT) scans with findings in specimens obtained at open lung biopsy and autopsy. The following HRCT findings were observed: (a) an accumulation of small cystic spaces with thick walls, (b) air bronchiolograms within areas of intense lung attenuation, (c) rugged pleural surfaces, (d) irregularly thickened pulmonary vessels, (e) bronchial wall thickening, and (f) slightly increased lung attenuation. Macroscopic honeycombing correlating with small cystic spaces was demonstrated at HRCT and pathologic examination. Air bronchiolograms in the areas of intense lung attenuation (ie, microscopic honeycombing) corresponded to dilated bronchioles (> 1 mm in diameter) with fibrosis. Irregularly thickened vessels and bronchial walls and irregular pleural surfaces were the result of fibrosis in the periphery of the secondary pulmonary lobules. Areas of slightly increased lung attenuation seen on the HRCT scans correlated with patchy alveolar septal fibrosis or inflammation. The authors conclude that microscopic honeycombing and a perilobular distribution in UIP may be clearly identified with HRCT.
引用
收藏
页码:337 / 342
页数:6
相关论文
共 27 条
[1]   CT IN THE DIAGNOSIS OF INTERSTITIAL LUNG-DISEASE [J].
BERGIN, CJ ;
MULLER, NL .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1985, 145 (03) :505-510
[2]   CHRONIC LUNG-DISEASES - SPECIFIC DIAGNOSIS BY USING CT [J].
BERGIN, CJ ;
COBLENTZ, CL ;
CHILES, C ;
BELL, DY ;
CASTELLINO, RA .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1989, 152 (06) :1183-1188
[3]  
BERGIN CJ, 1986, AJR, V148, P8
[4]  
CARRINGTON CB, 1978, NEW ENGL J MED, V298, P801, DOI 10.1056/NEJM197804132981501
[5]   IDIOPATHIC PULMONARY FIBROSIS - CLINICAL, HISTOLOGIC, RADIOGRAPHIC, PHYSIOLOGIC, SCINTIGRAPHIC, CYTOLOGIC, AND BIOCHEMICAL ASPECTS [J].
CRYSTAL, RG ;
FULMER, JD ;
ROBERTS, WC ;
MOSS, ML ;
LINE, BR ;
REYNOLDS, HY .
ANNALS OF INTERNAL MEDICINE, 1976, 85 (06) :769-788
[6]  
Heitzman E. R, 1984, LUNG RADIOLOGICPATHO
[7]  
ITOH H, 1986, BIOMEDICAL IMAGING, P249
[8]  
KATZENSTEIN ALA, 1976, AM J PATHOL, V85, P210
[9]  
Kitaichi M, 1986, Clin Dermatol, V4, P108, DOI 10.1016/0738-081X(86)90039-8
[10]  
KITAICHI M, 1989, INTERSTITIAL PNEUMON, P189