Literature DB >> 23495888

Cervical rudimentary meningocele in adulthood.

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.

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Year:  2013        PMID: 23495888     DOI: 10.3171/2013.2.SPINE12603

Source DB:  PubMed          Journal:  J Neurosurg Spine        ISSN: 1547-5646


  2 in total

1.  Missed limited dorsal myeloschisis: an unfortunate cause for recurrent tethered cord syndrome.

Authors:  Sandip Chatterjee; K Santosh Mohan Rao
Journal:  Childs Nerv Syst       Date:  2015-06-07       Impact factor: 1.475

2.  True Cervicothoracic Meningocele: A Rare and Benign Condition.

Authors:  Bruno L Pessoa; Yara Lima; Marco Orsini
Journal:  Neurol Int       Date:  2015-12-31
  2 in total

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