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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

  • Czech description

Classification

  • Type

    J<sub>SC</sub> - Article in a specialist periodical, which is included in the SCOPUS database

  • CEP classification

  • OECD FORD branch

    30203 - Respiratory systems

Result continuities

  • Project

  • 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

  • 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