Langerhans cell histiocytosis of bone in children: a long-term retrospective study

J Pediatr Orthop B. 2012 Sep;21(5):457-62. doi: 10.1097/BPB.0b013e32835367c0.

Abstract

Langerhans cell histiocytosis is rare and frequently involves the bone. We retrospectively reviewed the orthopaedic aspects (symptoms, localizations, treatments) and the long-term outcome [disease status, overall survival (OS), event-free survival (EFS)] of 121 patients (June 1968-December 2009). The main symptom was local pain. The orthopaedic treatment was mainly conservative. The most frequent localization was osseous monofocal (62% of monosystemic diseases). Monosystemic and osseous monofocal localizations, treatment after 1991 (OS, P=0.007; EFS, P=0.03) and age older than 2 years (OS, P=0.003; EFS, P=0.001) were prognostic factors that were positively associated with survival. Oncologic treatment has improved over time, translating into better survival. A biopsy is often mandatory.

MeSH terms

  • Adolescent
  • Bone Diseases / diagnosis*
  • Bone Diseases / mortality
  • Bone Diseases / therapy
  • Child
  • Child, Preschool
  • Combined Modality Therapy
  • Female
  • Histiocytosis, Langerhans-Cell / diagnosis*
  • Histiocytosis, Langerhans-Cell / mortality
  • Histiocytosis, Langerhans-Cell / therapy
  • Humans
  • Infant
  • Infant, Newborn
  • Italy / epidemiology
  • Male
  • Pain
  • Prognosis
  • Retrospective Studies
  • Survival Rate
  • Treatment Outcome