Multicentric parenchymal xanthogranuloma in a child: case report and review of the literature

Neurosurgery. 2002 Dec;51(6):1493-8; discussion 1498.

Abstract

Objective and importance: Xanthogranulomas of the central nervous system are rare, and asymptomatic lesions are often identified in autopsies. We report the first case of a multicentric, cystic, intraparenchymal xanthogranuloma, involving both the supra- and infratentorial compartments, in a 16-month-old girl.

Clinical presentation: The clinical presentation consisted of a focal motor seizure in an otherwise healthy infant.

Intervention: Gross total removal of the infratentorial lesion was accomplished via a midline suboccipital craniotomy.

Conclusion: Intracranial xanthogranulomas are rare, and limited experience with the diagnosis of these lesions has been reported. Although most cases are asymptomatic, this case involves a symptomatic, multicentric, intraparenchymal xanthoma in a pediatric patient. Our review of the literature provides further insights regarding the clinical, radiological, and pathological behavior of these lesions and examines the available treatment strategies.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Craniotomy
  • Cysts / diagnosis
  • Cysts / pathology
  • Cysts / surgery
  • Female
  • Humans
  • Infant
  • Xanthogranuloma, Juvenile / diagnosis*
  • Xanthogranuloma, Juvenile / pathology
  • Xanthogranuloma, Juvenile / surgery