Pleuroparenchymal fibroelastosis as a manifestation of chronic lung rejection?

نویسندگان

  • Takako Hirota
  • Masaki Fujita
  • Takemasa Matsumoto
  • Takao Higuchi
  • Takeshi Shiraishi
  • Masato Minami
  • Meinoshin Okumura
  • Kazuki Nabeshima
  • Kentaro Watanabe
چکیده

Statement of Interest: Statements of interest for S. Birring and I. Pavord can be found at www.erj.ersjournals.com/site/misc/ statements.xhtml REFERENCES 1 Pavord ID, Chung KF. Management of chronic cough. Lancet 2008; 371: 1375–1384. 2 Morice AH, McGarvey L, Pavord ID. Recommendations for the management of cough in adults. Thorax 2006; 61: 1–24. 3 Birring SS, Fleming T, Matos S, et al. The Leicester Cough Monitor: preliminary validation of an automated cough detection system in chronic cough. Eur Respir J 2008; 31: 1013–1018. 4 Matos S, Birring SS, Pavord ID, et al. Detection of cough signals in continuous audio recordings using hidden Markov models. IEEE Trans Biomed Eng 2006; 53: 1078–1083. 5 Prudon B, Birring SS, Vara DD, et al. Cough and glottic-stop reflex sensitivity in health and disease. Chest 2005; 127: 550–557. 6 Birring SS, Matos S, Patel RB, et al. Cough frequency, cough sensitivity and health status in patients with chronic cough. Respir Med 2006; 100: 1105–1109. 7 Pavord ID, Pizzichini MM, Pizzichini E, et al. The use of induced sputum to investigate airway inflammation. Thorax 1997; 52: 498–501. 8 Birring SS, Prudon B, Carr AJ, et al. Development of a symptom specific health status measure for patients with chronic cough: Leicester Cough Questionnaire (LCQ). Thorax 2003; 58: 339–343. 9 Morice AH, Lowry R, Brown MJ, et al. Angiotensin-converting enzyme and the cough reflex. Lancet 1987; 2: 1116–1118.

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References 1 Frankel SK, Cool CD, Lynch DA, et al. Idiopathic pleuroparenchymal fibroelastosis: description of a novel clinicopathologic entity. Chest 2004; 126: 2007–2013. 2 Travis WD, Costabel U, Hansell DM, et al. An official American Thoracic Society/European Respiratory Society statement: update of the international multidisciplinary classification of the idiopathic interstitial pneumonias...

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Two cases of pleuroparenchymal fibroelastosis diagnosed with transbronchial lung biopsy

Idiopathic pleuroparenchymal fibroelastosis (PPFE) is a rare subset of idiopathic interstitial pneumonias (IIPs). Here we present two patients with PPFE in which the histology was confirmed with transbronchial lung biopsy (TBLB). The 25-year-old and 64-year-old men were both slender with a long history of pulmonary upper lobe fibrosis and a marked restrictive impairment. Although the imaging fi...

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Pleuroparenchymal fibroelastosis presenting with pneumothorax

A 47-year-old woman presented with spontaneous right side pneumothorax. Image studies showed consolidations and reticular opacities involving the pleural and subpleural regions of bilateral lungs. Wedge biopsy specimens of right upper, middle and lower lobes showed fibrosis of the visceral pleura and subpleural area in all three lobes, more significant in the upper lobe. Elastic Van Gieson stai...

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Pleuroparenchymal fibroelastosis: is it also an idiopathic entity?

Pleuroparenchymal fibroelastosis (PPFE) is a rare disease that has been recently included in the updated consensus on idiopathic interstitial pneumonias. It shares some clinical features with other chronic interstitial pneumonias (dyspnea, dry cough), and is radiologically characterized by pleural and subpleural parenchymal fibrosis and elastosis, mainly in the upper lobes. The main histologica...

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Pleuroparenchymal fibroelastosis from a consecutive database: a rare disease entity?

Pleuroparenchymal fibroelastosis (PPFE) is a rare condition characterised by predominantly upper lobe involvement with pleural fibrosis and subjacent parenchymal fibroelastosis [1, 2]. Idiopathic PPFE (IPPFE), which was included in the rare idiopathic interstitial pneumonias (IIPs) in the update of the international multidisciplinary classification of IIPs published in 2013 [3], was first descr...

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عنوان ژورنال:
  • The European respiratory journal

دوره 41 1  شماره 

صفحات  -

تاریخ انتشار 2013