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

1 served in SSc-ILD, whereas IPF is defined by usual interstitial pneumonia.

2 (95% CI 54-96) for underlying biopsy-proven usual interstitial pneumonia.

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

4 cterized by the histopathological pattern of usual interstitial pneumonia.

5 for confirmation of histological patterns of usual interstitial pneumonia.

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

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

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

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

10 fibrosis, asks the question: is it all about usual interstitial pneumonia?

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

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

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

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

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

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

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

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

19 Usual interstitial pneumonia and nonspecific interstitia

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

21 al interstitial pneumonia, indeterminate for usual interstitial pneumonia, and alternative diagnosis;

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

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

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

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

26 Usual interstitial pneumonia by HRCT (P < 0.0002) and ba

27 ressive Pulmonary Fibrosis, Thin-Section CT, Usual Interstitial Pneumonia (C) RSNA, 2024.

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

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

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

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

32 5 and 63 after idiopathic pulmonary fibrosis/usual interstitial pneumonia fibroblast injection, patch

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

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

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

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

37 Although usual interstitial pneumonia generally responds poorly t

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

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

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

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

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

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

44 The classifier identified usual interstitial pneumonia in transbronchial lung biop

45 and SLB for patterns of definite or probable usual interstitial pneumonia, indeterminate for usual in

46 and the exploration of PF phenotypes beyond usual interstitial pneumonia/IPF.

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

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

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

50 The histological pattern, known as usual interstitial pneumonia, is the archetype of progre

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

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

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

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

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

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

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

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

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

60 se patients who had possible or inconsistent usual interstitial pneumonia on HRCT, the classifier sho

61 Patients with usual interstitial pneumonia or nonspecific interstitial

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

63 ncluded patients with ILD with a nondefinite usual interstitial pneumonia pattern (on high-resolution

64 A usual interstitial pneumonia pattern is a hallmark of id

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

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

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

68 acyte, San Francisco, CA, USA) to identify a usual interstitial pneumonia pattern.

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

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

71 by severity into affected (all criteria for usual interstitial pneumonia present) and less affected

72 less affected (some but not all criteria for usual interstitial pneumonia present).

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

74 A molecular usual interstitial pneumonia signature can be identified

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

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

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

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

79 lmonary fibrosis (IPF) requires a pattern of usual interstitial pneumonia to be present on high-resol

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

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

82 diagnosis of the histopathologic pattern of usual interstitial pneumonia (UIP) and clinical IPF.

83 mages were quantified, and guideline-defined usual interstitial pneumonia (UIP) and fibrotic hypersen

84 and angiogenesis markers between histologic usual interstitial pneumonia (UIP) and non-UIP were asse

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

86 nosis, particularly when typical features of usual interstitial pneumonia (UIP) are identified.

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

88 e high-resolution chest scan (HRCT), and the usual interstitial pneumonia (UIP) histologic pattern.

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

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

91 rize specific features of TBLC predictive of usual interstitial pneumonia (UIP) in corresponding SLB

92 The usual interstitial pneumonia (UIP) incidence was higher

93 ic interstitial lung diseases that share the usual interstitial pneumonia (UIP) injury pattern.

94 Rationale: Usual interstitial pneumonia (UIP) is the defining morph

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

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

97 s were scored for the extent of fibrosis and usual interstitial pneumonia (UIP) pattern.

98 /ALAT diagnostic guidelines for IPF based on usual interstitial pneumonia (UIP) patterns, the pooled

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

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

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

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

103 Usual interstitial pneumonia (UIP), the pathologic corre

104 ained and validated in the identification of usual interstitial pneumonia (UIP)-like features on HRCT

105 ng features that overlap with IPF, including usual interstitial pneumonia (UIP)-pattern disease chara

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

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

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