Spinal cord subependymoma mimicking syringomyelia in a child: a case report.
Masahiro OishiHironori FujisawaKatsuhiro TsuchiyaYoshio NakashimaPublished in: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery (2020)
Spinal cord subependymomas (SCSEs) in children are extremely rare, and no reports distinguishing SCSEs from syringomyelia have been published. We report a case of a 10-year-old boy who presented with torticollis, scoliosis, as well as pain that had begun in the posterior portion of the neck and progressed to the right shoulder and upper arm. Magnetic resonance imaging showed an intramedullary cyst-like lesion with the same signal intensity as that of cerebrospinal fluid. Idiopathic syringomyelia with scoliosis was first suspected, and a syrinx-subarachnoid space shunt was performed. After surgery, the lesion was slightly smaller; however, 2 years after surgery, it had re-grown, causing excruciating pain but no other symptoms. A second surgery was performed, and gross total resection was achieved. Pathological evaluation revealed SCSE. SCSE needs to be considered as a differential diagnosis for spinal centric cyst-like lesions in children.
Keyphrases
- spinal cord
- neuropathic pain
- magnetic resonance imaging
- chronic pain
- cerebrospinal fluid
- spinal cord injury
- young adults
- pain management
- minimally invasive
- mental health
- single cell
- coronary artery bypass
- acute coronary syndrome
- surgical site infection
- systematic review
- magnetic resonance
- emergency department
- depressive symptoms
- randomized controlled trial
- contrast enhanced
- adverse drug
- rotator cuff
- electronic health record