Intersticiální plicní procesy a granulomatózy asociované s běžným variabilním imunodeficitem
[Interstitial lung diseases and granulomatoses associated common variable immunodeficiency]
Language Czech Country Czech Republic Media print
Document type Journal Article, Review
PubMed
25813254
PII: 51593
- MeSH
- Agammaglobulinemia etiology MeSH
- Common Variable Immunodeficiency complications diagnosis epidemiology MeSH
- Bronchiectasis etiology MeSH
- Adult MeSH
- Lung Diseases, Interstitial etiology MeSH
- Humans MeSH
- Pneumonia etiology MeSH
- Prevalence MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
Common variable immunodeficiency disorder belongs to the most common primary human immunodeficiencies and it is characterized by primary defective immunoglobulin production. Hypogammaglobulinemia manifests in every age, usually in adult people. There is no gender predisposition. The prevalence is 1 : 25 000-1 : 50 000. The ethiopathogenesis of the majority of CVIDs is unknown. The main clinical respiratory symptoms include recurrent respiratory infects, especially bacterial etiology, sinusitis, bronchitis, pneumonia, leading to bronchiectasis and lung fibrosis. Interstitial lung fibrosis and granulomatosis often manifest at diagnosis of CVID and they are negative prognostic factors of the disease.