Skip to main content

Advertisement

Log in

Neuromuscular hamartoma: imaging features of a rare paediatric craniofacial tumour

  • Case Report
  • Published:
Pediatric Radiology Aims and scope Submit manuscript

Abstract.

Neuromuscular hamartoma (also referred to as neuromuscular choristoma or benign triton tumour) has not previously been described in the radiological literature. It is a rare benign lesion composed of mature elements of striated muscle and neural tissue. We report a case of neuromuscular hamartoma involving the skull base, nasopharynx, orbit and maxilla in a 2.5-year-old child who presented with facial swelling. The CT and MRI appearances of this unusual soft-tissue tumour are emphasized, together with a discussion of the pathological findings, differential diagnosis and review of the literature.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Electronic Publication

Rights and permissions

Reprints and permissions

About this article

Cite this article

Oeppen, R.S., Harden, S.P. & Argent, J.D. Neuromuscular hamartoma: imaging features of a rare paediatric craniofacial tumour. Ped Radiol 33, 50–52 (2003). https://doi.org/10.1007/s00247-002-0788-2

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00247-002-0788-2

Navigation