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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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發(fā)表于 2025-3-21 17:18:18 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Idiopathic Pulmonary Fibrosis
副標(biāo)題Advances in Diagnost
編輯Hiroyuki Nakamura,Kazutetsu Aoshiba
視頻videohttp://file.papertrans.cn/462/461072/461072.mp4
概述Introducing new developments such as serum makers that are highly specific to IPF, the establishment of systematic diagnosis imaging and antifibrotic agent.Each chapter addresses key issues under disc
圖書封面Titlebook: Idiopathic Pulmonary Fibrosis; Advances in Diagnost Hiroyuki Nakamura,Kazutetsu Aoshiba Book 2016 Springer Japan 2016 HRCT.IIP.IPF.KL-6.SP-
描述From epidemiology and pathogenesis to disease management, this book reviews our current understanding of and provides up-to-date information of Idiopathic Pulmonary Fibrosis (IPF). A subtype of Idiopathic Interstitial Pneumonias (IIP), IPF is one of the most elusive and intractable respiratory disease to date and its triggering factors remain unclear. However, new developments such as serum markers that are highly specific to IPF (i.e. KL-6, SP-A, and SP-D), the establishment of systematic diagnostic imaging (HRCT) and accumulated reports of treatment using an antifibrotic agent (pirfenidone) are slowly improving our understanding of the disease. Edited by an established authority in the field and written by experts, this book will be valuable to not only to beginning learners but also to physicians, instructors and researchers whose work involves IIPs. With each chapter exploring critical questions, with unresolved issues and future prospects, the book offers a valuable resource for understanding issues such as the newly proposed entity of interstitial pneumonia with emphysema (combined pulmonary fibrosis and emphysema: CPFE) and the mechanism of how so many IIP sufferers develop
出版日期Book 2016
關(guān)鍵詞HRCT; IIP; IPF; KL-6; SP-A; SP-D
版次1
doihttps://doi.org/10.1007/978-4-431-55582-7
isbn_softcover978-4-431-56281-8
isbn_ebook978-4-431-55582-7
copyrightSpringer Japan 2016
The information of publication is updating

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發(fā)表于 2025-3-21 20:33:21 | 只看該作者
Combined Pulmonary Fibrosis and Emphysema (CPFE)orbidity, mortality and management of CPFE. The establishments of definition, classification and staging of CPFE, including delineation of boundaries between IPF and CPFE, also are required. Better understanding of CPFE will be able to develop future therapeutic strategies.
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發(fā)表于 2025-3-22 04:00:20 | 只看該作者
High-Resolution Computed Tomography of Honeycombing and IPF/UIPneycombing) is a key finding in the diagnosis of IPF/UIP, but experienced radiologists sometimes disagree in judging honeycomb lung at HRCT. Early diagnosis of IPF/UIP requires establishment of diagnostic criteria other than honeycombing and investigation of HRCT findings that correspond with temporal and spatial heterogeneity.
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Pharmacotherapy of Acute Exacerbation of IPF (Corticosteroids, Immunosuppressants, and Direct Hemopef the efficacy of these treatment methods, and no AE-IPF treatment method of high evidence level is included in the guidelines available at present. It would be desirable to facilitate clarification of the pathophysiology of AE-IPF and to carry out RCTs with the cooperation of multiple facilities.
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urface by cationic polyelectrolyte and depends on the SDS concentration and prehistory of the first adsorbed layer. The desorption study showed that in all cases the partial desorption of SDS took place, the value of this desorption depended on the structure of the first adsorbed layer and SDS conce
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