| Literature DB >> 23495888 |
Hao Wang1, Wenhua Yu, Zuyong Zhang, Yongmin Lu, Xiao Li.
Abstract
Almost all cases of cervical spinal dysraphism published to date have involved cystic lesions and were treated in very early childhood. The authors describe a unique case of a 21-year-old woman who harbored a solid cervical rudimentary meningocele. On preoperative CT and MR images, a cutaneous solid mass was shown to be connected to intraspinal contents by a stalk traversing the C-3 lamina defect. The authors resected the cutaneous mass and released the tethering neural band from the vertical axis of the spinal cord without causing injury. Pathological examination demonstrated a dense collagenous tissue containing clusters of meningocytes and psammoma bodies in the cutaneous mass. This rare entity, a spinal dysraphism with a benign natural history, may contribute to the current classification of cervical spinal dysraphism.Entities:
Mesh:
Year: 2013 PMID: 23495888 DOI: 10.3171/2013.2.SPINE12603
Source DB: PubMed Journal: J Neurosurg Spine ISSN: 1547-5646