| Literature DB >> 10352417 |
W J Hader1, P Steinbok, K Poskitt, G Hendson.
Abstract
The authors present a patient with diastematomyelia and a spinal intramedullary teratoma, remote from the split cord malformation. A split cord malformation at the L2-L3 level was initially discovered during investigations for thoracic congenital scoliosis, and this was treated surgically. The teratoma, which was at the level of the scoliosis, went undiagnosed until neurological deterioration occurred many years later. Surgical removal of the teratoma resulted in return to normal function. The potential for coexisting congenital anomalies at separate levels of the spinal cord must be considered in radiological investigations of a developmental spinal lesion.Entities:
Mesh:
Year: 1999 PMID: 10352417 DOI: 10.1159/000028782
Source DB: PubMed Journal: Pediatr Neurosurg ISSN: 1016-2291 Impact factor: 1.162