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特发性胸膜肺实质弹力纤维增生症 被引量：2

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摘要 2004年Frankel等[1]首先提出特发性胸膜肺实质弹力纤维增生症（idiopathic pleuroparenchymal fibroelastosis,IPPFE）的概念。Frankel等[1]研究发现,5例IPPFE患者肺组织的病理改变不同于传统的特发性间质性肺炎,镜下表现以胸膜及其下肺实质内弹性纤维增生为特征;胸部影像学表现以两上肺为主的胸膜增厚;临床上以活动后气促为主要症状。其临床-影像-组织病理特点不能归类到现有的特发性间质性肺炎（idiopathic interstitial pneumonia,IIP）中,因此命名为IPPFE。回顾既往文献,早在1992年,日本学者Amitani等[2]曾提出过特发性肺上叶纤维化的概念,
作者 桂贤华 蔡后荣
机构地区 南京大学医学院附属鼓楼医院呼吸内科
出处 《中国呼吸与危重监护杂志》 CAS 2014年第6期624-627,共4页 Chinese Journal of Respiratory and Critical Care Medicine
关键词 特发性间质性肺炎 弹力纤维增生症 胸膜增厚 肺实质 FRANKEL 胸部影像学表现 pneumonia 组织病理特点
分类号 R561 [医药卫生—呼吸系统]
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参考文献23

  • 1Frankel SK, Cool CD, Lynch DA, et al. pleuroparenchymal fibroelastosis : description of clinicopathologic entity. Chest, 2004,126 : 2007 -2013.
  • 2Amitani R, Niimi A, Kuse F. Idiopathic pulmonary upper lobe fibrosis ( IPUF). Kokyu, 1992,11:693-699.
  • 3冯瑞娥.一种新的特发性间质性肺炎类型：特发性胸膜间质弹力纤维化[J].中华结核和呼吸杂志,2013,36(5):329-330. 被引量：8
  • 4Becker CD, Gil J, Padilla ML. Idiopathic pleuroparenchymal fibroelastosis:an unrecognized or misdiagnosed entity? Mod Pathol, 2008,21:784-787.
  • 5Kusagaya H, Nakamura Y, Kono M, et al. Idiopathic pleuroparenchymal fibroelastosis : consideration of clinicopathological entity in a series of Japanese patients. BMC Pulm Med,2012 ,12 :72.
  • 6Watanabe K, Nagata N, Kitasato Y, et al. Rapid decrease in forced vital capacity in patients with idiopathic pulmonary upper lobe fibrosis. Respir Investig,2012,50 : 88-97.
  • 7Piciucchi S,Tomassetti S, Casoni G, et al. High resolution CT and histological findings in idiopathic pleuroparenchymal fibroelastosis:features and differential diagnosis. Respir Res,2011,12 : 111.
  • 8yon der Thiisen JH, Hansell DM, Tominaga M, et al. Pleuroparenchymal fibmelastosis in patients with pulmonary disease secondary to hone marrow transplantation. Mod Pathol, 2011,24: 1633-1639.
  • 9Maehuca JS, Niazi M, Diaz-Fuentes G. Pleumparenehymal fibroelastosis presenting as a hypermetabolie lung nodule. J Bmnehology Interv Pulmonol,2011,18 :65-68.
  • 10An official American Thoracic Society/European Respiratory Society Statement: Update of the International Muhidisciplinary Classification of the Idiopathic Interstitial Pneumonias. Am J Respir Crit Care Meal,2013,188:733-748.

二级参考文献6

  • 1Frankel SK, Cool CD, Lynch DA, et al. Idiopathic pleuroparenchymal fibroelastosis : description of a novel clinicopathologic entity. Chest, 2004, 126:2007-2013.
  • 2Beeker CD, Gil J, Padilla ML. Idiopathic pleuroparenehymal fibroelastosis: an unrecognized or misdiagnosed entity'?.. Mod pathol, 2008, 21:784-787.
  • 3Piciueehi S, Tomassetti S, Casoni G, et at. High resolution CT and histological findings in idiopathic pleuroparenchymal fibroelastosis: features and differential diagnosis. Respir Res, 2011, 23:111.
  • 4vonder Thtisen JH, Hansell DM, Tominaga M, et al. Pleuroparenchymal fibroelastosis in patients with pulmortary disease secondary to bone marrow transplantation. Mod Pathol, 2011, 24: 1633 -1639.
  • 5Watanabe K, Nagata N, Kitasato Y, et al. Rapid decrease in forced vital capacity in patients with idiopathic puhnonary upper lobe fibrosis. Respir Investig, 2012, 50:88-97.
  • 6American Thoracic Society, European Respiratory Society. American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society ( ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors, June 2001 and by the ERS Executive Committee, June 2001. Am J Respir Crit Care Mcd, 2002, 165:277-304.

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中国呼吸与危重监护杂志
2014年 第6期

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