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...
Saved in:
| Main Authors: | , , , |
|---|---|
| Format: | Book |
| Published: |
Association of Nurses Technicians and Midwives,
2020-01-01T00:00:00Z.
|
| Subjects: | |
| Online Access: | Connect to this object online. |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|