Vanishing Lung Syndrome in a Cystic Fibrosis Patient
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F17%3A10373780" target="_blank" >RIV/00216208:11130/17:10373780 - isvavai.cz</a>
Alternative codes found
RIV/00064203:_____/17:10373780
Result on the web
<a href="https://doi.org/10.1016/j.arbres.2017.01.015" target="_blank" >https://doi.org/10.1016/j.arbres.2017.01.015</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.arbres.2017.01.015" target="_blank" >10.1016/j.arbres.2017.01.015</a>
Alternative languages
Result language
angličtina
Original language name
Vanishing Lung Syndrome in a Cystic Fibrosis Patient
Original language description
Vanishing lung syndrome is a rare condition characterized by unilateral or bilateral asymmetric upper lobe involvement with the formation of multiple large bullae replacing normal pulmonary architecture and compressing surrounding parenchyma. In this paper, we report the case of a male cystic fibrosis (CF) patient with severe sinopulmonary disease, malnutrition, diabetes mellitus and asthenozoospermia. He was diagnosed with CF at 3 years of age due to malnutrition and recurrent respiratory infections. His sweat chloride concentration was 101 mmol/L and CFTR gene mutations were F508del and 2935del11. At the age of 30, he was evaluated for a lung transplant and chest imaging studies were performed. Previous chest X-rays had showed slowly progressing changes in the upper areas of both lung fields over the past 3 years. In patients with CF, the typical CT picture is bronchiectasis, bronchial wall thickening, mucus plugging, atelectasis, consolidation and air trapping.2 Emphysematous and bullous changes are not consistent with CF lung disease. Our patient was a never-smoker and had normal levels of serum α1-antitrypsin, with no symptoms of other diseases that may be complicated by vanishing lung syndrome or giant bullae (e.g. sarcoidosis, granulomatosis with polyangiitis or Marfan and Ehlers-Danlos syndromes).
Czech name
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Czech description
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Classification
Type
J<sub>SC</sub> - Article in a specialist periodical, which is included in the SCOPUS database
CEP classification
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OECD FORD branch
30203 - Respiratory systems
Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Archivos de Bronconeumología
ISSN
0300-2896
e-ISSN
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Volume of the periodical
53
Issue of the periodical within the volume
8
Country of publishing house
ES - SPAIN
Number of pages
1
Pages from-to
451
UT code for WoS article
000406648200011
EID of the result in the Scopus database
2-s2.0-85025432376