Temporal bone histiocytosis in children: a systematic review

Francesca Galluzzi1, Werner Garavello2

  • 1Department of Otorhinolaryngology, Fondazione IRCCS San Gerardo Dei Tintori, Monza, Italy.

Abstract

Insights

Temporal bone histiocytosis (TBH) in children presents with ear symptoms and osteolytic lesions. Management requires a multidisciplinary approach with long-term follow-up for potential recurrences and complications.

Area of Science:

  • Pediatric Otolaryngology
  • Pediatric Radiology
  • Pediatric Endocrinology

Background:

  • Temporal bone histiocytosis (TBH) is a rare condition affecting children.
  • Early diagnosis and treatment are crucial for managing this condition.

Purpose of the Study:

  • To analyze the diagnosis, treatment, and outcomes of temporal bone histiocytosis (TBH) in children.
  • To highlight the importance of a multidisciplinary approach and long-term follow-up.

Main Methods:

  • Systematic review adhering to PRISMA guidelines.
  • Literature search conducted on PubMed and Embase databases.
  • Risk of bias assessed using the MINOR Score.

Main Results:

  • Eight retrospective studies involving 84 children were analyzed.
  • Common symptoms include otorrhea, otalgia, and recurrent otitis; pituitary involvement with diabetes insipidus was noted.
  • CT scans showed osteolytic lesions; MRI aided in detecting intracranial lesions. Recurrence rate was 20.2%.

Conclusions:

  • Management of pediatric TBH necessitates a multidisciplinary strategy.
  • Otolaryngologists play a key role in early diagnosis and surgical intervention.
  • Long-term follow-up is essential for monitoring recurrences and otological complications.