ライフサイエンスコーパス: usual interstitial pneumonia

1 ing pneumonia, and 18 as subtypes other than usual interstitial pneumonia.

2 cterized by the histopathological pattern of usual interstitial pneumonia.

3 for confirmation of histological patterns of usual interstitial pneumonia.

4 -resolution CT images are not definitive for usual interstitial pneumonia.

5 pithelial areas of fibrosis in patients with usual interstitial pneumonia.

6 sisted of 238 patients with biopsy confirmed usual interstitial pneumonia.

7 d CT findings that were more compatible with usual interstitial pneumonia.

8 mples were identified by the expert panel as usual interstitial pneumonia, 23 as non-specific interst

9 met high-resolution CT criteria for possible usual interstitial pneumonia (94.0%, 86.7-98.0).

10 We retrospectively examined 80 patients with usual interstitial pneumonia and 29 patients with nonspe

11 Desaturation was common (44 of 83 usual interstitial pneumonia and 8 of 22 nonspecific int

12 As some patients with usual interstitial pneumonia and an underlying collagen

13 onary fibrosis and a histologic diagnosis of usual interstitial pneumonia and evaluated the prognosti

14 at regional sites familiar with patterns of usual interstitial pneumonia and management of idiopathi

15 d only minor gene expression changes between usual interstitial pneumonia and nonspecific interstitia

16 Usual interstitial pneumonia and nonspecific interstitia

17 dds prognostic information for patients with usual interstitial pneumonia and nonspecific interstitia

18 ed as usual interstitial pneumonia, possible usual interstitial pneumonia, and inconsistent with usua

19 raphy, the narrowed pathologic definition of usual interstitial pneumonia, and recognition of the pro

20 t of fibrosis, histopathological features of usual interstitial pneumonia, and reduced survival in pa

21 Exceptions were two patients classified with usual interstitial pneumonia at CT but with nonspecific

22 pathic interstitial pneumonia (IIP), such as usual interstitial pneumonia, can be impervious to moder

23 For patients with usual interstitial pneumonia, change in forced vital cap

24 rt of 36 patients with histologically proven usual interstitial pneumonia (CPI, p < 0.0005; FVC, p =

25 tients with the severest form of IIP, namely usual interstitial pneumonia, exhibited the greatest gen

26 5 and 63 after idiopathic pulmonary fibrosis/usual interstitial pneumonia fibroblast injection, patch

27 oxin (IL13-PE), the proliferation of primary usual interstitial pneumonia fibroblasts was inhibited t

28 nterstitial pneumonia, and inconsistent with usual interstitial pneumonia) for confirmation of histol

29 n of the prognostic importance of separating usual interstitial pneumonia from other idiopathic inter

30 develop a molecular test that distinguishes usual interstitial pneumonia from other interstitial lun

31 Although usual interstitial pneumonia generally responds poorly t

32 group; 52 deaths occurred in the idiopathic usual interstitial pneumonia group (log rank; p = 0.005)

33 in the collagen vascular disease-associated usual interstitial pneumonia group; 52 deaths occurred i

34 Patients with idiopathic usual interstitial pneumonia had a higher median profusi

35 ents who met high-resolution CT criteria for usual interstitial pneumonia had histologically confirme

36 ts with collagen vascular disease-associated usual interstitial pneumonia have fewer fibroblastic foc

37 (OLB, n = 1) patterns typical for idiopathic usual interstitial pneumonia (idiopathic UIP) were enter

38 Idiopathic pulmonary fibrosis (IPF)/usual interstitial pneumonia is a ravaging condition of

39 lopment of a genomic signature that predicts usual interstitial pneumonia is feasible.

40 A histologic feature of usual interstitial pneumonia is the presence of fibrobla

41 uding nonspecific interstitial pneumonia and usual interstitial pneumonia, making diagnosis extremely

42 Four major CT patterns were identified: usual interstitial pneumonia (n = 26), nonspecific inter

43 st would predict mortality for patients with usual interstitial pneumonia (n = 83) and nonspecific in

44 histologically confirmed as not or possible usual interstitial pneumonia (negative predictive value

45 urgical lung biopsies from 108 patients with usual interstitial pneumonia (nine with collagen vascula

46 entities: idiopathic pulmonary fibrosis with usual interstitial pneumonia, nonspecific interstitial p

47 sts grown from idiopathic pulmonary fibrosis/usual interstitial pneumonia, nonspecific interstitial p

48 thritis is associated with four CT patterns: usual interstitial pneumonia, nonspecific interstitial p

49 ic from collagen vascular disease-associated usual interstitial pneumonia (odds ratio 8.31; 95% confi

50 Patients with usual interstitial pneumonia or nonspecific interstitial

51 ncluding nonspecific interstitial pneumonia, usual interstitial pneumonia, organizing pneumonia, lymp

52 A usual interstitial pneumonia pattern is a hallmark of id

53 clinical setting, for patients with possible usual interstitial pneumonia pattern on high resolution

54 interstitial lung disease without a typical usual interstitial pneumonia pattern on high-resolution

55 ecure a definitive histological diagnosis of usual interstitial pneumonia pattern.

56 itial pneumonia had histologically confirmed usual interstitial pneumonia (positive predictive value

57 e value of high-resolution CT (classified as usual interstitial pneumonia, possible usual interstitia

58 can Thoracic Association guidelines (81.3%), usual interstitial pneumonia secondary to autoimmune con

59 Last, tissue slices from human lung with usual interstitial pneumonia submitted to mechanical for

60 is a more accurate prognostic determinant in usual interstitial pneumonia than an individual pulmonar

61 inconsistent high-resolution CT pattern for usual interstitial pneumonia that was histologically con

62 In patients with usual interstitial pneumonia, the presence of desaturati

63 having idiopathic pulmonary fibrosis of the usual interstitial pneumonia type (IPF/UIP) were reviewe

64 sified by two pulmonary histopathologists as usual interstitial pneumonia (UIP) (47%), NSIP (36%), or

65 d to the histopathologic distinction between usual interstitial pneumonia (UIP) and nonspecific inter

66 We prospectively studied 87 patients with usual interstitial pneumonia (UIP) confirmed by surgical

67 terans organizing pneumonia (BOOP) in 1, and usual interstitial pneumonia (UIP) in 1.

68 Patients with usual interstitial pneumonia (UIP) in all lobes were cat

69 variety of patterns suggestive of underlying usual interstitial pneumonia (UIP) or nonspecific inters

70 sis at surgical lung biopsy and to compare a usual interstitial pneumonia (UIP) pattern at CT with su

71 eview showed a heterogeneous group including usual interstitial pneumonia (UIP), desquamative interst

72 Idiopathic interstitial pneumonias comprise usual interstitial pneumonia (UIP), nonspecific intersti

73 primary fibroblast lines from patients with usual interstitial pneumonia (UIP), nonspecific intersti

74 s reticulation, without atypical features of usual interstitial pneumonia (UIP), on high-resolution c

75 Usual interstitial pneumonia (UIP), the pathologic corre

76 inical evaluation of patients with suspected usual interstitial pneumonia (UIP).

77 identified a population of fibroblasts from usual interstitial pneumonia (UIP)/idiopathic pulmonary

78 Patients with usual interstitial pneumonia were more likely to have a