Solitary, extracutaneous, skull-based juvenile xanthogranuloma

Pediatr Blood Cancer. 2010 Aug;55(2):380-2. doi: 10.1002/pbc.22534.

Abstract

We report a case of an 18-month-old female who presented an occipital bone lesion with progressive growth. Imaging studies showed a left extradural, skull-based tumor partially occupying the posterior fossa. Histopathological and immunohistochemical studies confirmed a juvenile xanthogranuloma (JXG). Partial surgical resection, chemotherapy, and conformational radiotherapy were used. Exclusive extracutaneous JXG with an intracranial, vertebral, or skull-based localization is extremely rare.

Publication types

  • Case Reports

MeSH terms

  • Bone Neoplasms / diagnosis*
  • Bone Neoplasms / pathology
  • Bone Neoplasms / therapy
  • Combined Modality Therapy
  • Diagnostic Imaging
  • Female
  • Humans
  • Infant
  • Skull Base
  • Treatment Outcome
  • Xanthogranuloma, Juvenile / diagnosis*
  • Xanthogranuloma, Juvenile / pathology
  • Xanthogranuloma, Juvenile / therapy