Cicatricial organising pneumonia associated with fibrosing interstitial pneumonia - a clinicopathological study 2

• Material Type: 博士論文
• ISSN: 1365-2559
• Title: Cicatricial organising pneumonia associated with fibrosing interstitial pneumonia - a clinicopathological study
• Volume: 80 2
• Author/Editor: 財前, 圭晃
• Author Heading: 財前, 圭晃
• Publication, Distribution, etc.: John Wiley & Sons Ltd.
• Publication Date: 2022-03-18
• Publication Date (W3CDTF): 2022-03-18
• Alternative Title: 瘢痕化する器質化肺炎は線維化性間質性肺炎と相関する - 臨床病理学的検討
• Periodical title: Histopathology
• Degree grantor/type: Nagasaki University (長崎大学)
• Date Granted: 2022-03-18
• Date Granted (W3CDTF): 2022-03-18
• Dissertation Number: 甲医歯薬第1418号
• Degree Type: 博士(医学)
• Conferring No. (Dissertation): 甲医歯薬第1418号
• Text Language Code: jpn
• Subject Heading: cicatricial organising pneumonia; fibrosing organising pneumonia; idiopathic pulmonary fibrosis; interstitial pneumonia
• Target Audience: 一般
• Note (General): Aims: The recent recognition of cicatricial organising pneumonia (ciOP) indicates that the ciOP may resemble or simulate fibrotic interstitial pneumonia; however, there has been great uncertainty regarding the affected populations, pathogenesis, clinical relevance and characteristics. In this study, we compared the characteristics of fibrotic interstitial pneumonia with and without ciOP.Methods and results: We enrolled 121 patients from the consultation archive whose pathological findings were fibrotic interstitial pneumonia and for whom follow-up clinical data were available. We reviewed these cases histopathologically and classified them according to whether or not they showed ciOP. We compared the clinicopathological features between the two groups. CiOP, histopathologically characterised by deposition of dense collagenous fibres within the alveolar space without destruction of the lung structure, was found in 48 patients (39.7%). None of the cases with ciOP experienced acute exacerbation during 12 months’ follow-up. The group with ciOP had more severe diffusion impairment but this, together with restrictive ventilatory impairment, improved significantly compared to the group without ciOP.Conclusion: CiOP is a histopathological finding commonly found in fibrotic interstitial pneumonia. It does not relate to acute exacerbation or decrease in pulmonary function.; 長崎大学学位論文 学位記番号:博(医歯薬)甲第1418号 学位授与年月日:令和4年3月18日; Author: Yoshiaki Zaizen, Kazuhiro Tabata, Yasuhiko Yamano, Reoto Takei, Kensuke Kataoka, Akira Shiraki, Koichi Nishimura, Kazuto Furuyama, Andrey Bychkov, Tomoaki Hoshino, Takeshi Johkoh, Yasuhiro Kondoh & Junya Fukuoka; Citation: Histopathology, 80(2), pp. 279-290; 2022; identifier:Nagasaki University (長崎大学), 博士(医学) (2022-03-18); http://hdl.handle.net/10069/00041421
• DOI: info:doi/10.1111/his.14427; https://doi.org/info:doi/10.1111/his.14427
• Persistent ID (NDL): info:ndljp/pid/12356308; https://dl.ndl.go.jp/pid/12356308
• Collection: 障害者向け資料
• Collection (Materials For Handicapped People:1): テキストデータ
• Collection (particular): 国立国会図書館デジタルコレクション > デジタル化資料 > 博士論文; https://dl.ndl.go.jp/collections/A00014
• Acquisition Basis: 博士論文（自動収集）
• Date Accepted (W3CDTF): 2022-10-11T11:55:44+09:00
• Date Created (W3CDTF): 2022-05-31
• Format (IMT): PDF
• Access Restrictions: 国立国会図書館内限定公開
• Service for the Digitized Contents Transmission Service: 図書館・個人送信対象外
• Availability of remote photoduplication service: 可
• Related Material (URI): http://hdl.handle.net/10069/00041421
• Periodical Title (URI): http://hdl.handle.net/10069/00041575
• Data Provider (Database): 国立国会図書館 : 国立国会図書館デジタルコレクション; https://dl.ndl.go.jp