Multisystemic langerhans-cell histiocytosis with dominant lesions of the lung parenchyma
Langerhans cell histiocytosis (LCH) is a rare disease of unknown aetiology characterized by abnormal monoclonal proliferation of CD1a+/ CD207+ myeloid dendritic cells (Langerhans cells) in various organs, including bones, skin, lymph nodes, liver, lungs, central nervous system (CNS). Pulmonary Lange...
Na minha lista:
| Principais autores: | , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | sérvio |
| Publicado em: |
Association of Nurses Technicians and Midwives
2020-01-01
|
| coleção: | Sestrinska reč |
| Assuntos: | |
| Acesso em linha: | https://scindeks-clanci.ceon.rs/data/pdf/0354-8422/2020/0354-84222080026J.pdf |
| Tags: |
Sem tags, seja o primeiro a adicionar uma tag!
|