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.
Similar content being viewed by others
Author information
Authors and Affiliations
Additional information
Electronic Publication
Rights 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
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/s00247-002-0788-2