ライフサイエンスコーパス: interstitial pneumonia

1 squamative interstitial pneumonia, and acute interstitial pneumonia.

2 58 consecutive cases of suspected idiopathic interstitial pneumonia.

3 ether to establish a diagnosis of idiopathic interstitial pneumonia.

4 ost commonly encountered fibrotic idiopathic interstitial pneumonia.

5 l pneumonia and 29 patients with nonspecific interstitial pneumonia.

6 .08) compared with patients with nonspecific interstitial pneumonia.

7 usual interstitial pneumonia and nonspecific interstitial pneumonia.

8 seline features for patients with idiopathic interstitial pneumonia.

9 as associated with induced MIC expression in interstitial pneumonia.

10 of 238 patients with biopsy confirmed usual interstitial pneumonia.

11 indings that were more compatible with usual interstitial pneumonia.

12 so with hepatitis, conjunctivitis, and viral interstitial pneumonia.

13 ding SIV-induced encephalitis and lentivirus interstitial pneumonia.

14 ological and physiological manifestations of interstitial pneumonia.

15 ry fibrosis (IPF) is a progressive and fatal interstitial pneumonia.

16 of graft-versus-host disease (GVHD) and the interstitial pneumonia.

17 ad parotid gland enlargement and lymphocytic interstitial pneumonia.

18 eumonia, and 18 as subtypes other than usual interstitial pneumonia.

19 ed by the histopathological pattern of usual interstitial pneumonia.

20 nfirmation of histological patterns of usual interstitial pneumonia.

21 itial pneumonia and management of idiopathic interstitial pneumonia.

22 ution CT images are not definitive for usual interstitial pneumonia.

23 set of respiratory distress caused by severe interstitial pneumonia.

24 monary fibrosis (IPF) is a fatal progressive interstitial pneumonia.

25 ial areas of fibrosis in patients with usual interstitial pneumonia.

26 features, including severe skin disease and interstitial pneumonia.

27 usual interstitial pneumonia and nonspecific interstitial pneumonia.

28 evelopment of several subtypes of idiopathic interstitial pneumonia.

29 < 0.001) than for other subgroups of chronic interstitial pneumonias.

30 ed to treat acute exacerbation of idiopathic interstitial pneumonias.

31 sociated with sporadic and familial fibrotic interstitial pneumonias.

32 l interstitial pneumonia, 23 as non-specific interstitial pneumonia, 16 as hypersensitivity pneumonit

33 were identified by the expert panel as usual interstitial pneumonia, 23 as non-specific interstitial

34 requency of 34% among subjects with familial interstitial pneumonia, 38% among subjects with idiopath

35 in the lung among 83 subjects with familial interstitial pneumonia, 492 subjects with idiopathic pul

36 conditions (11.5%), or fibrosing nonspecific interstitial pneumonia (7.2%).

37 gh-resolution CT criteria for possible usual interstitial pneumonia (94.0%, 86.7-98.0).

38 interstitial pneumonia (UIP) or nonspecific interstitial pneumonia, a review of the histopathologic

39 ively established, it seems that nonspecific interstitial pneumonia accounts for a large proportion o

40 del infection is required for development of interstitial pneumonia after allogeneic BMT.

41 rolling the development of P. carinii-driven interstitial pneumonia after either syngeneic or allogen

42 ryptogenic organizing pneumonia (COP), acute interstitial pneumonia (AIP), and lymphoid interstitial

43 nterstitial pneumonia/fibrosis (NSIP), acute interstitial pneumonia (AIP), bronchiolitis, bronchiolit

44 families with 2 or more cases of idiopathic interstitial pneumonia among first-degree family members

45 ts in the paclitaxel plus gemcitabine group (interstitial pneumonia, anaphylaxis, and severe neutrope

46 nt protein C (L188Q SFTPC) found in familial interstitial pneumonia and (ii) intratracheal treatment

47 rospectively examined 80 patients with usual interstitial pneumonia and 29 patients with nonspecific

48 Desaturation was common (44 of 83 usual interstitial pneumonia and 8 of 22 nonspecific interstit

49 I, 3.8 to 113.7), respectively, for familial interstitial pneumonia and 9.0 (95% CI, 6.2 to 13.1) and

50 scan, we detected linkage between idiopathic interstitial pneumonia and a 3.4-Mb region of chromosome

51 As some patients with usual interstitial pneumonia and an underlying collagen vascul

52 fibrosis and a histologic diagnosis of usual interstitial pneumonia and evaluated the prognostic sign

53 the SLB group, mostly idiopathic nonspecific interstitial pneumonia and hypersensitivity pneumonitis,

54 romoter of MUC5B is associated with familial interstitial pneumonia and idiopathic pulmonary fibrosis

55 n mice with chronic hyperglycemia results in interstitial pneumonia and increased susceptibility to i

56 Affected pigs exhibited severe interstitial pneumonia and lymphoid depletion.

57 gional sites familiar with patterns of usual interstitial pneumonia and management of idiopathic inte

58 Usual interstitial pneumonia and nonspecific interstitial pneu

59 ognostic information for patients with usual interstitial pneumonia and nonspecific interstitial pneu

60 minor gene expression changes between usual interstitial pneumonia and nonspecific interstitial pneu

61 ts into the early pathogenesis of idiopathic interstitial pneumonia and provide an ongoing opportunit

62 pared with fibroblast lines from nonspecific interstitial pneumonia and respiratory bronchiolitis/int

63 stitial lung diseases, including nonspecific interstitial pneumonia and usual interstitial pneumonia,

64 omplex lung diseases, notably the idiopathic interstitial pneumonias and small airways diseases, owes

65 hocytic interstitial pneumonia, desquamative interstitial pneumonia, and acute interstitial pneumonia

66 th usual interstitial pneumonia, nonspecific interstitial pneumonia, and chronic hypersensitivity pne

67 om infected CCL3(-/-) mice suffered a milder interstitial pneumonia, and fewer immune cells were reco

68 usual interstitial pneumonia, possible usual interstitial pneumonia, and inconsistent with usual inte

69 the narrowed pathologic definition of usual interstitial pneumonia, and recognition of the prognosti

70 ibrosis, histopathological features of usual interstitial pneumonia, and reduced survival in patients

71 al interstitial pneumonia (UIP), nonspecific interstitial pneumonia, and respiratory bronchiolitis-in

72 iopsy had histologic findings of nonspecific interstitial pneumonia, and the seventh had bronchioliti

73 o diagnose, especially, in the case in which interstitial pneumonia appears in the course of gold the

74 ly to corticosteroid therapy, other forms of interstitial pneumonia are often steroid responsive and

75 Idiopathic interstitial pneumonias are a diverse group of lung dise

76 ogic analysis; one patient, with nonspecific interstitial pneumonia at CT but desquamative interstiti

77 gic analysis; and one patient, with lymphoid interstitial pneumonia at CT but nonspecific interstitia

78 ions were two patients classified with usual interstitial pneumonia at CT but with nonspecific inters

79 interstitial pneumonia at CT but nonspecific interstitial pneumonia at pathologic analysis.

80 nterstitial pneumonia at CT but desquamative interstitial pneumonia at pathologic analysis; and one p

81 stitial pneumonia at CT but with nonspecific interstitial pneumonia at pathologic analysis; one patie

82 s: usual interstitial pneumonia, nonspecific interstitial pneumonia, bronchiolitis, and organizing pn

83 Both patients had associated nonspecific interstitial pneumonia but no signs of malignancy.

84 mice in response to P carinii does not cause interstitial pneumonia, but irradiation of the host befo

85 hat resolved to multifocal lymphohistiocytic interstitial pneumonia by 28 days.

86 This interstitial pneumonia can be caused by the accumulation

87 This interstitial pneumonia can occur in infected mice after

88 interstitial pneumonia (IIP), such as usual interstitial pneumonia, can be impervious to modern ster

89 The interstitial pneumonia caused by allogeneic BMT and P ca

90 -however, it did not stop the development of interstitial pneumonia caused by the infiltration of hos

91 For patients with usual interstitial pneumonia, change in forced vital capacity

92 accinated or received empty vector developed interstitial pneumonia characterized by a marked alveoli

93 prolonged and exacerbated P. carinii-driven interstitial pneumonia characterized by eosinophilia and

94 terstitial pneumonia and 8 of 22 nonspecific interstitial pneumonia; chi square, p = 0.39).

95 Idiopathic interstitial pneumonias comprise usual interstitial pneu

96 36 patients with histologically proven usual interstitial pneumonia (CPI, p < 0.0005; FVC, p = 0.002;

97 more extensive in patients with nonspecific interstitial pneumonia CT pattern (P =.028).

98 Usual interstitial pneumonia and nonspecific interstitial pneumonia CT patterns overlapped; GGO was m

99 isks of graft-versus-host disease (GVHD) and interstitial pneumonia decreased over time, but the risk

100 pneumonia, organizing pneumonia, lymphocytic interstitial pneumonia, desquamative interstitial pneumo

101 ulmonary fibrosis or idiopathic non-specific interstitial pneumonia diagnosed within the preceding 6

102 l interstitial pneumonia (UIP), desquamative interstitial pneumonia (DIP), nonspecific interstitial p

103 interstitial pneumonia (NSIP), desquamative interstitial pneumonia (DIP), respiratory bronchiolitis-

104 nia (UIP) (47%), NSIP (36%), or desquamative interstitial pneumonia (DIP)/respiratory bronchiolitis-a

105 ma-/- splenocytes which was characterized by interstitial pneumonia, eosinophilia, and multinucleated

106 with the severest form of IIP, namely usual interstitial pneumonia, exhibited the greatest gene and

107 63 after idiopathic pulmonary fibrosis/usual interstitial pneumonia fibroblast injection, patchy inte

108 Adoptively transferred nonspecific interstitial pneumonia fibroblasts caused a more diffuse

109 IL13-PE), the proliferation of primary usual interstitial pneumonia fibroblasts was inhibited to a mu

110 ve interstitial pneumonia (DIP), nonspecific interstitial pneumonia/fibrosis (NSIP), acute interstiti

111 Fibrotic idiopathic interstitial pneumonias (fIIP) are a group of fatal lung

112 such as Birt-Hogg-Dube syndrome, lymphocytic interstitial pneumonia, follicular bronchiolitis, and li

113 itial pneumonia, and inconsistent with usual interstitial pneumonia) for confirmation of histological

114 he prognostic importance of separating usual interstitial pneumonia from other idiopathic interstitia

115 op a molecular test that distinguishes usual interstitial pneumonia from other interstitial lung dise

116 Although usual interstitial pneumonia generally responds poorly to cort

117 ; 52 deaths occurred in the idiopathic usual interstitial pneumonia group (log rank; p = 0.005).

118 e collagen vascular disease-associated usual interstitial pneumonia group; 52 deaths occurred in the

119 Patients with idiopathic usual interstitial pneumonia had a higher median profusion of

120 ho met high-resolution CT criteria for usual interstitial pneumonia had histologically confirmed usua

121 h collagen vascular disease-associated usual interstitial pneumonia have fewer fibroblastic foci and

122 ncy virus-infected children with lymphocytic interstitial pneumonia have human immunodeficiency virus

123 n = 1) patterns typical for idiopathic usual interstitial pneumonia (idiopathic UIP) were entered int

124 Idiopathic interstitial pneumonia (IIP) and its familial variants a

125 lmonary fibrotic diseases such as idiopathic interstitial pneumonia (IIP), but it is not presently cl

126 Severe forms of idiopathic interstitial pneumonia (IIP), such as usual interstitial

127 ant in categorizing patients with idiopathic interstitial pneumonia (IIP).

128 Idiopathic interstitial pneumonias (IIPs) are a collection of pulmo

129 The idiopathic interstitial pneumonias (IIPs) are a seemingly disconnec

130 ciety (ATS/ERS) classification of idiopathic interstitial pneumonias (IIPs) defined seven specific en

131 Idiopathic interstitial pneumonias (IIPs) have a progressive and of

132 , white individuals with fibrotic idiopathic interstitial pneumonias (IIPs; n = 1,616) and controls (

133 ndrome virus (PRRSV), which induces an acute interstitial pneumonia in pigs.

134 tations in the proSP-C sequence with chronic interstitial pneumonias in children and adults.

135 ients with other types of idiopathic chronic interstitial pneumonias including NSIP.

136 ymphocytes and plasma cells in RA-associated interstitial pneumonia (IP) in comparison with idiopathi

137 spiratory tract infection (URTI; n=3) or RSV interstitial pneumonia (IP; n=12), all of whom also rece

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

139 t of a genomic signature that predicts usual interstitial pneumonia is feasible.

140 The diagnosis of idiopathic interstitial pneumonia is made by means of correlation o

141 Nonspecific interstitial pneumonia is now better defined.

142 diopathic pulmonary fibrosis and nonspecific interstitial pneumonia is recognized to be heterogeneous

143 A histologic feature of usual interstitial pneumonia is the presence of fibroblastic f

144 milar to that associated with the idiopathic interstitial pneumonias is not known.

145 s (IPF), a chronic and progressive fibrosing interstitial pneumonia, is a fatal lung disease with a m

146 Analyses of the microscopic-interstitial-pneumonia-lesion scores (0 to 6) revealed t

147 of children with AIDS-associated lymphocytic interstitial pneumonia (LIP) are unknown, we studied the

148 e interstitial pneumonia (AIP), and lymphoid interstitial pneumonia (LIP).

149 nonspecific interstitial pneumonia and usual interstitial pneumonia, making diagnosis extremely diffi

150 stic infections, suggesting that lymphocytic interstitial pneumonia may reflect an effective antivira

151 [range, 38-93 years]), 244 with nonspecific interstitial pneumonia (men, 79; women, 165; median age,

152 s with acute lung injury (n = 7) and chronic interstitial pneumonia (n = 14) were stained for detecti

153 interstitial pneumonia (n = 26), nonspecific interstitial pneumonia (n = 19), bronchiolitis (n = 11),

154 erstitial pneumonia (n = 83) and nonspecific interstitial pneumonia (n = 22).

155 our major CT patterns were identified: usual interstitial pneumonia (n = 26), nonspecific interstitia

156 ld predict mortality for patients with usual interstitial pneumonia (n = 83) and nonspecific intersti

157 logically confirmed as not or possible usual interstitial pneumonia (negative predictive value 18.3%,

158 l lung biopsies from 108 patients with usual interstitial pneumonia (nine with collagen vascular dise

159 s is associated with four CT patterns: usual interstitial pneumonia, nonspecific interstitial pneumon

160 es: idiopathic pulmonary fibrosis with usual interstitial pneumonia, nonspecific interstitial pneumon

161 own from idiopathic pulmonary fibrosis/usual interstitial pneumonia, nonspecific interstitial pneumon

162 Surgical lung biopsies disclosed nonspecific interstitial pneumonia (NSIP) in 18 of 22 patients (81.8

163 Patients with nonspecific interstitial pneumonia (NSIP) in all lobes were categori

164 al interstitial pneumonia (UIP), nonspecific interstitial pneumonia (NSIP), desquamative interstitial

165 interstitial pneumonia (UIP) and nonspecific interstitial pneumonia (NSIP), the most commonly encount

166 topathologic patterns, including nonspecific interstitial pneumonia (NSIP).

167 0.73 [0.68-0.78]); moderate for non-specific interstitial pneumonia (NSIP; kappaw=0.42 [0.37-0.49]);

168 demonstrating several subtypes of idiopathic interstitial pneumonia occurring within the same familie

169 m collagen vascular disease-associated usual interstitial pneumonia (odds ratio 8.31; 95% confidence

170 In chronic interstitial pneumonia, only rare type II pneumocytes (<

171 Patients with usual interstitial pneumonia or nonspecific interstitial pneum

172 Interstitial pneumonias or lymphoid organ lesions, simil

173 among first-degree family members (familial interstitial pneumonia, or FIP), and identified 111 fami

174 is/usual interstitial pneumonia, nonspecific interstitial pneumonia, or histologically normal biopsie

175 ng nonspecific interstitial pneumonia, usual interstitial pneumonia, organizing pneumonia, lymphocyti

176 .001), and 27 of 244 (11.1%) had nonspecific interstitial pneumonia (P < .001).

177 controls (allelic association with familial interstitial pneumonia, P=1.2x10(-15); allelic associati

178 A usual interstitial pneumonia pattern is a hallmark of idiopath

179 al setting, for patients with possible usual interstitial pneumonia pattern on high resolution CT, su

180 stitial lung disease without a typical usual interstitial pneumonia pattern on high-resolution comput

181 a definitive histological diagnosis of usual interstitial pneumonia pattern.

182 interstitial pneumonia from other idiopathic interstitial pneumonia patterns have profoundly changed

183 pneumonia had histologically confirmed usual interstitial pneumonia (positive predictive value 97.3%,

184 e of high-resolution CT (classified as usual interstitial pneumonia, possible usual interstitial pneu

185 phocyte depletion of mesenteric lymph nodes, interstitial pneumonia, psoriatic skin lesions, and neur

186 with biopsies from patients with nonspecific interstitial pneumonia, respiratory bronchiolitis-inters

187 oracic Association guidelines (81.3%), usual interstitial pneumonia secondary to autoimmune condition

188 st, tissue slices from human lung with usual interstitial pneumonia submitted to mechanical force sho

189 ore accurate prognostic determinant in usual interstitial pneumonia than an individual pulmonary func

190 ation developed a more protracted and severe interstitial pneumonia than that of normal mice given P

191 sistent high-resolution CT pattern for usual interstitial pneumonia that was histologically confirmed

192 In patients with usual interstitial pneumonia, the presence of desaturation was

193 rus-infected individuals develop lymphocytic interstitial pneumonia, the roles of host and viral fact

194 d-resistant acute exacerbation of idiopathic interstitial pneumonias treated with blood purification

195 g idiopathic pulmonary fibrosis of the usual interstitial pneumonia type (IPF/UIP) were reviewed.

196 In chronic interstitial pneumonia, type II pneumocytes proliferate

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

198 he histopathologic distinction between usual interstitial pneumonia (UIP) and nonspecific interstitia

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

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

201 Patients with usual interstitial pneumonia (UIP) in all lobes were categoriz

202 y of patterns suggestive of underlying usual interstitial pneumonia (UIP) or nonspecific interstitial

203 surgical lung biopsy and to compare a usual interstitial pneumonia (UIP) pattern at CT with survival

204 showed a heterogeneous group including usual interstitial pneumonia (UIP), desquamative interstitial

205 ry fibroblast lines from patients with usual interstitial pneumonia (UIP), nonspecific interstitial p

206 athic interstitial pneumonias comprise usual interstitial pneumonia (UIP), nonspecific interstitial p

207 culation, without atypical features of usual interstitial pneumonia (UIP), on high-resolution compute

208 Usual interstitial pneumonia (UIP), the pathologic correlate o

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

210 ified a population of fibroblasts from usual interstitial pneumonia (UIP)/idiopathic pulmonary fibros

211 in rheumatic diseases, including nonspecific interstitial pneumonia, usual interstitial pneumonia, or

212 conditions, including nonspecific pneumonia, interstitial pneumonia, viral pneumonia, consolidation,

213 Patients with usual interstitial pneumonia were more likely to have a statis

214 usual interstitial pneumonia or nonspecific interstitial pneumonia who desaturated had a significant

215 s characterized by a moderate self-resolving interstitial pneumonia with bronchiolitis of 21 days in

216 at first presented itself radiologically as interstitial pneumonia with pleural effusion and clinica

217 MERS-CoV caused a multifocal, mild to marked interstitial pneumonia, with virus replication occurring