| Literature DB >> 29848524 |
Linda-Marie Ustaris1, Roberta Seidman2, Tejwant Bindra3, Ratna Basak4,5.
Abstract
A 4-year-old girl with no significant medical or family history presented with toe walking, leg pain, unsteady gait and frequent falls for 2 months. Examination revealed upper motor neuron signs in the lower extremities. Laboratory tests were normal including creatinephosphokinase and lactate dehydrogenase. Brain and lumbar spine MRI were normal. MRI cervical and thoracic spine showed a large intradural and extradural mass arising from the right C7 nerve root, widening of the neural canal with evidence of cord compression. She underwent C6-C7 laminectomy with excision of the tumour. Pathology revealed spindle cell tumour with extensive expression of S100 protein and CD56, with Ki-67 proliferation index of 1%-2% consistent with benign schwannoma. She made an excellent recovery following surgery and physiotherapy sessions. Review of literature shows rare reported case of schwannoma prior to the third decade of life. © BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.Entities:
Keywords: neurosurgery; paediatrics; pathology; spinal cord
Mesh:
Year: 2018 PMID: 29848524 PMCID: PMC5990059 DOI: 10.1136/bcr-2017-223589
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X