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...
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| Hauptverfasser: | , , , |
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| Format: | Artigo |
| Sprache: | Serbisch |
| Veröffentlicht: |
Association of Nurses Technicians and Midwives
2020-01-01
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| Schriftenreihe: | Sestrinska reč |
| Schlagworte: | |
| Online-Zugang: | https://scindeks-clanci.ceon.rs/data/pdf/0354-8422/2020/0354-84222080026J.pdf |
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