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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]

. 2022 Summer ; 68 (E-2) : 11-21.

Language Czech Country Czech Republic Media print

Document type Journal Article

Links

PubMed 36208940
PII: 131860

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.

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