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...
Guardat en:
| Autors principals: | , , , |
|---|---|
| Format: | Artigo |
| Idioma: | serbi |
| Publicat: |
Association of Nurses Technicians and Midwives
2020-01-01
|
| Col·lecció: | Sestrinska reč |
| Matèries: | |
| Accés en línia: | https://scindeks-clanci.ceon.rs/data/pdf/0354-8422/2020/0354-84222080026J.pdf |
| Etiquetes: |
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|