Long-term outcome, clinical course and treatment approaches of paediatric langerhans cell histiocytosis: A greek reference centre report.
Vasiliki TzotzolaLoizos PetrikkosVassilios PapadakisGeorgia MitropoulouCharikleia KelaidiEfthymios DimitriadisSophia PolychronopoulouPublished in: Acta paediatrica (Oslo, Norway : 1992) (2021)
LCH survival rates significantly increased in our cohort over time. Reactivation occurred in 18.2% patients, but no late neurodegeneration was found. The prognostic value of single system disease status vs. multisystem LCH was confirmed.