Pathology of IPF
Fig. 7.1 Histology of UIP. (a) Panoramic view. Patchy involvement and perilobular dense fibrosis with structural remodeling. Bar: 1 cm. Hematoxylin-eosin staining (HE). (b, c) Fibroblastic focus on dense fibrosis (arrow)….
RESPIRATORY
Acute Exacerbation of Interstitial Pneumonia After Pulmonary Resection for Lung Cancer
Fig. 15.1 A typical case of acute exacerbation after pulmonary resection for lung cancer. (a) A solid mass of adenocarcinoma in the middle lobe. (b) Basal slice of the CT…
Common Pathways in IPF and Lung Cancer
MicroRNA Tumorigenesis IPF development Related molecules miR-21 ↑ ↑ TPM1, PDCD4, PTEN,TGFβ, NFIB, mapsin, Spry-2, MARCKS MMPs, RECK, SMAD2, SMAD7, FGF2 Let-7 ↓ ↓ TGFβ, HMGA2, SMAD3, RAS, CDC25A miR-155…
Pharmacotherapy of IPF (Corticosteroids, Immunosuppressants, Etc.)
Treatment Recommended Strength of recommendation Quality of evidence Pharmacologic therapies Corticosteroid monotherapy No Strong ⊕○○○ Colchicine No Strong ⊕○○○ Cyclosporine A No Strong ⊕○○○ Corticosteroid + immunomodulatory No Strong ⊕○○○ Corticosteroid + azathioprine + acetylcysteine Majority…
Combined Pulmonary Fibrosis and Emphysema (CPFE)
Study Number of patients with CPFE/with IIPs Prevalence (%) Akira et al. [8] 15/80 18.8 Choi et al. [9] 66/254 26.0 Copley et al. [10] 76/212 35.8 Doherty et al….
Non-pharmacological Therapy for IPF
Fig. 11.1 Oxygen time courses in pulmonary capillary when diffusion is normal and abnormal (e.g., because of thickening of the blood–gas barrier by disease) (Reprinted with permission of Wolters Kluwer…
Specific Serum Markers of IPF
Fig. 5.1 Structures of SP-A and SP-D. Monomeric and oligomeric structures of SP-A and SP-D. Monomeric structures can be conceptually divided into four major structural domains: a short N-terminal segment…
Acute Exacerbation of IPF
Fig. 3.1 Clinical disease courses in patients with IPF. The typical natural history of IPF is the slow progression of the disease with a median survival period of approximately 3 years…
Pharmacotherapy of Acute Exacerbation of IPF (Corticosteroids, Immunosuppressants, and Direct Hemoperfusion with Polymyxin)
© Springer Japan 2016Hiroyuki Nakamura and Kazutetsu Aoshiba (eds.)Idiopathic Pulmonary Fibrosis10.1007/978-4-431-55582-7_12 12. Pharmacotherapy of Acute Exacerbation of IPF (Corticosteroids, Immunosuppressants, and Direct Hemoperfusion with Polymyxin) Are High-Dose Steroid Therapy, Other Immunosuppressant Therapy, and PMX Therapy…
Definition of IPF
Fig. 1.1 Diagnostic algorithm for idiopathic pulmonary fibrosis (IPF). Patients with suspected IPF should be carefully evaluated for identifiable causes of interstitial lung disease (ILD). In the absence of an…
