Titlebook: Idiopathic Pulmonary Fibrosis; Advances in Diagnost Hiroyuki Nakamura,Kazutetsu Aoshiba Book 2016 Springer Japan 2016 HRCT.IIP.IPF.KL-6.SP-

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Pathology of IPFh a peripheral lobular distribution. The natural history of UIP is unclear, but attempts have been made to elucidate it. The complication of acute and subacute worsening or exacerbation has been discussed as an important part of the natural history of UIP. The major differential diagnoses of UIP are

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Non-pharmacological Therapy for IPFtive treatments. The symptoms and complications of IPF such as dyspnea, exercise intolerance, and depression severely impair patients’ quality of life (QOL) and decrease social participation. Although evidence for the benefit of pulmonary rehabilitation (PR) in IPF is limited, it has recently been r

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Combined Pulmonary Fibrosis and Emphysema (CPFE)l and radiological features from both pulmonary fibrosis and emphysema. Tobacco smoking may be situated at a major cause and differentiate prognosis of CPFE associated with PH and lung cancer from that of pulmonary fibrosis or emphysema alone. Further studies are needed to ascertain the aetiology, m

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Common Pathways in IPF and Lung Cancercancer and IPF are often characterized by high comorbidity, and IPF is therefore considered to be a risk factor for the incidence of lung cancer. On the other hand, its high comorbidity recalls the existence of a common pathway in the pathogenesis and progression of both diseases. However, lung canc

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Acute Exacerbation of Interstitial Pneumonia After Pulmonary Resection for Lung Cancerecause these therapies including surgery may trigger acute exacerbation (AE) and are confounded by the progressive nature and poor prognoses of ILDs. We conducted a large (. = 1,763) retrospective multi-institutional study to identify the predictors of AE and to identify the predictors of long-term