Elisabeth Bendstrup

Diagnostic criteria and possible treatment of idiopathic pulmonary fibrosis

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

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Diagnostic criteria and possible treatment of idiopathic pulmonary fibrosis. / Prior, Thomas; Hilberg, Ole; Bendstrup, Elisabeth.

In: Ugeskrift for Læger , Vol. 176, No. 22, 26.05.2014.

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

Harvard

Prior, T, Hilberg, O & Bendstrup, E 2014, 'Diagnostic criteria and possible treatment of idiopathic pulmonary fibrosis', Ugeskrift for Læger , vol. 176, no. 22.

APA

Prior, T., Hilberg, O., & Bendstrup, E. (2014). Diagnostic criteria and possible treatment of idiopathic pulmonary fibrosis. Ugeskrift for Læger , 176(22).

CBE

Prior T, Hilberg O, Bendstrup E. 2014. Diagnostic criteria and possible treatment of idiopathic pulmonary fibrosis. Ugeskrift for Læger . 176(22).

MLA

Prior, Thomas, Ole Hilberg, and Elisabeth Bendstrup. "Diagnostic criteria and possible treatment of idiopathic pulmonary fibrosis". Ugeskrift for Læger . 2014. 176(22).

Vancouver

Prior T, Hilberg O, Bendstrup E. Diagnostic criteria and possible treatment of idiopathic pulmonary fibrosis. Ugeskrift for Læger . 2014 May 26;176(22).

Author

Prior, Thomas ; Hilberg, Ole ; Bendstrup, Elisabeth. / Diagnostic criteria and possible treatment of idiopathic pulmonary fibrosis. In: Ugeskrift for Læger . 2014 ; Vol. 176, No. 22.

Bibtex

@article{2b833cab18cf41c2922acb2236e4f877,
title = "Diagnostic criteria and possible treatment of idiopathic pulmonary fibrosis",
abstract = "Pleuroparenchymal fibroelastosis is an idiopathic interstitial pneumonia, recently recognized as a new entity by American Thoracic Society/European Respiratory Society. We present the first Danish cases of pleuroparenchymal fibroelastosis in two young sisters, who had complained of dyspnoea since childhood. Their lung function was reduced at referral (forced expiratory volume in 1st sec.: 36-43%, forced vital capacity: 34-41%, diffusing capacity for carbon monoxide: 35%). High resolution CT showed apical peripheral consolidation, pleural thickening, traction bronchiectasis and enlarged lymph nodes of both patients; compatible with pleuroparenchymal fibroelastosis. Due to low lung function, lung biopsies were not performed.",
author = "Thomas Prior and Ole Hilberg and Elisabeth Bendstrup",
year = "2014",
month = may,
day = "26",
language = "Dansk",
volume = "176",
journal = "Ugeskrift for L{\ae}ger ",
issn = "0041-5782",
publisher = "Den Almindelige Danske L{\ae}geforening",
number = "22",

}

RIS

TY - JOUR

T1 - Diagnostic criteria and possible treatment of idiopathic pulmonary fibrosis

AU - Prior, Thomas

AU - Hilberg, Ole

AU - Bendstrup, Elisabeth

PY - 2014/5/26

Y1 - 2014/5/26

N2 - Pleuroparenchymal fibroelastosis is an idiopathic interstitial pneumonia, recently recognized as a new entity by American Thoracic Society/European Respiratory Society. We present the first Danish cases of pleuroparenchymal fibroelastosis in two young sisters, who had complained of dyspnoea since childhood. Their lung function was reduced at referral (forced expiratory volume in 1st sec.: 36-43%, forced vital capacity: 34-41%, diffusing capacity for carbon monoxide: 35%). High resolution CT showed apical peripheral consolidation, pleural thickening, traction bronchiectasis and enlarged lymph nodes of both patients; compatible with pleuroparenchymal fibroelastosis. Due to low lung function, lung biopsies were not performed.

AB - Pleuroparenchymal fibroelastosis is an idiopathic interstitial pneumonia, recently recognized as a new entity by American Thoracic Society/European Respiratory Society. We present the first Danish cases of pleuroparenchymal fibroelastosis in two young sisters, who had complained of dyspnoea since childhood. Their lung function was reduced at referral (forced expiratory volume in 1st sec.: 36-43%, forced vital capacity: 34-41%, diffusing capacity for carbon monoxide: 35%). High resolution CT showed apical peripheral consolidation, pleural thickening, traction bronchiectasis and enlarged lymph nodes of both patients; compatible with pleuroparenchymal fibroelastosis. Due to low lung function, lung biopsies were not performed.

M3 - Tidsskriftartikel

C2 - 25352007

VL - 176

JO - Ugeskrift for Læger

JF - Ugeskrift for Læger

SN - 0041-5782

IS - 22

ER -