Intracranial fibroxanthoma in an infant: a case report

In Hee Chung1, Young Seok Lee, Na-Hye Myong

  • 1Department of Radiology, Dankook University Hospital, Choongnam, Korea.

Insights

A rare infantile fibroxanthoma in a six-month-old mimicked a meningioma on imaging. This central nervous system tumor presented unique US, MRI, and PET/CT features.

Area of Science:

  • Pediatric Neurology
  • Neuro-oncology
  • Diagnostic Imaging

Background:

  • Primary central nervous system fibroxanthomas are exceptionally rare pediatric neoplasms.
  • Differentiating these tumors from more common intracranial lesions is diagnostically challenging.

Observation:

  • A six-month-old infant presented with a cranial dural mass.
  • Ultrasound revealed a well-circumscribed, echogenic mass.
  • CT showed isoattenuation, PET/CT indicated hypometabolism, and MRI demonstrated heterogeneous T2 hyperintensity with intense contrast enhancement.

Findings:

  • The imaging features on ultrasound (US), magnetic resonance imaging (MRI), and positron emission tomography/computed tomography (PET/CT) closely resembled those of a meningioma.
  • The tumor originated from the cranial dura mater.

Implications:

  • This case highlights the importance of considering rare diagnoses in pediatric neuro-oncology.
  • Accurate interpretation of multimodal imaging is crucial for differentiating infantile fibroxanthoma from meningioma.
  • Early and precise diagnosis impacts timely and appropriate therapeutic strategies.

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