Vybrané závažné „hematologické“ syndromy u dospělých pacientů v intenzivní péči
[Selected severe „haematological“ syndromes in adult intensive care patients]
Language Czech Country Czech Republic Media print
Document type Review, Journal Article
PubMed
36575067
DOI
10.36290/vnl.2022.107
PII: 133157
- Keywords
- HLH, Lens-Associated Uveitis, antiphospholipid syndrome, anti‑glomerular basement membrane (anti‑GBM) antibodies, caplacizumab, catastrophic antiphospholipid syndrome, cytokine storm syndrome, diffuse alveolar haemorrhage, eculizumab, eculizumab, etoposide, haemolytic‑uremic syndrome, hemophagocytic lymphohistiocytosis, hemophagocytic syndrome, immunosuppressive therapy, macrophage activation syndrome, plasma exchange, ravulizumab, recombinant factor VIIa, rituximab, thrombosis, thrombotic microangiopathies, thrombotic microangiopathy, thrombotic thrombocytopenic purpura, vasculitis,
- MeSH
- Antiphospholipid Syndrome * complications diagnosis therapy MeSH
- Adult MeSH
- Humans MeSH
- Lymphohistiocytosis, Hemophagocytic * MeSH
- Thrombotic Microangiopathies * diagnosis MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
Haemophagocytic syndrome, diffuse alveolar haemorrhage, catastrophic antiphospholipid syndrome and various types of thrombotic microangiopathies are rare conditions with significant morbidity and mortality. A common feature is late diagnosis, which can affect the success of treatment. The aim of this review article is to summarize the basic diagnostic and therapeutic steps of the present subpopulation of critically ill patients.
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