Multisystemic langerhans-cell histiocytosis with dominant lesions of the lung parenchyma

• Main Authors: Javorac Jovan (Author), Živanović Dejan (Author), Ilić Miroslav (Author), Milenković Ana (Author)
• Format: Book
• Published: Association of Nurses Technicians and Midwives, 2020-01-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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...