Histiocytóza z Langerhansových buněk. Přehled příznaků, které přivádějí pacienty k lékařům všech medicínských odborností
[Langerhans cell histiocytosis (LCH). Overview of symptoms of LCH, which may lead the patients to any of these medical specialists]
Language Czech Country Czech Republic Media print
Document type Journal Article
PubMed
36208940
PII: 131860
- Keywords
- Langerhans cell histiocytosis,
- MeSH
- Adult MeSH
- Histiocytosis, Langerhans-Cell * diagnosis metabolism therapy MeSH
- Humans MeSH
- Lymph Nodes pathology MeSH
- Rare Diseases MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Publication type
- Journal Article MeSH
Langerhans cell histiocytosis (LCH) is a rare condition with incidence in adults 1-2/1 million, wherein Langerhans cells proliferate abnormally, adversely impacting organs including most frequently bones, skin, lungs, pituitary gland, lymph nodes, gums and other organs. The LCH course varies widely among patients from a self-limiting condition, to one that progresses. But LCH only very rarely culminates in death. To aim of this text is to review all possible symptoms and manifestations of this disease.