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Pediatric intervertebral disc calcification: A no touch lesion

Intervertebral disc calcification (IVDC), though rare, remains an important differential of pediatric spinal pain. A 7-year-old boy presented with sudden-onset severe neck pain and restricted movements. There was no definite history of trauma or infection. Imaging of the cervical spine showed calcif...

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Autores principales: Garg, Monika, Kumar, Sanyal, Satija, Bhawna, Gupta, Rajat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669470/
https://www.ncbi.nlm.nih.gov/pubmed/23741126
http://dx.doi.org/10.4103/0974-8237.110123
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author Garg, Monika
Kumar, Sanyal
Satija, Bhawna
Gupta, Rajat
author_facet Garg, Monika
Kumar, Sanyal
Satija, Bhawna
Gupta, Rajat
author_sort Garg, Monika
collection PubMed
description Intervertebral disc calcification (IVDC), though rare, remains an important differential of pediatric spinal pain. A 7-year-old boy presented with sudden-onset severe neck pain and restricted movements. There was no definite history of trauma or infection. Imaging of the cervical spine showed calcification of the intervertebral disc at C2–3 level, with significant posterior protrusion into the spinal canal causing compression of the cervical spinal cord. The child was kept on conservative management. The calcification and posterior protrusion showed near-complete resolution on 3-month follow-up. This case report emphasizes that childhood IVDC is a benign condition which commonly resolves spontaneously, without any surgical intervention and neurological sequelae.
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spelling pubmed-36694702013-06-05 Pediatric intervertebral disc calcification: A no touch lesion Garg, Monika Kumar, Sanyal Satija, Bhawna Gupta, Rajat J Craniovertebr Junction Spine Case Report Intervertebral disc calcification (IVDC), though rare, remains an important differential of pediatric spinal pain. A 7-year-old boy presented with sudden-onset severe neck pain and restricted movements. There was no definite history of trauma or infection. Imaging of the cervical spine showed calcification of the intervertebral disc at C2–3 level, with significant posterior protrusion into the spinal canal causing compression of the cervical spinal cord. The child was kept on conservative management. The calcification and posterior protrusion showed near-complete resolution on 3-month follow-up. This case report emphasizes that childhood IVDC is a benign condition which commonly resolves spontaneously, without any surgical intervention and neurological sequelae. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3669470/ /pubmed/23741126 http://dx.doi.org/10.4103/0974-8237.110123 Text en Copyright: © Journal of Craniovertebral Junction and Spine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Garg, Monika
Kumar, Sanyal
Satija, Bhawna
Gupta, Rajat
Pediatric intervertebral disc calcification: A no touch lesion
title Pediatric intervertebral disc calcification: A no touch lesion
title_full Pediatric intervertebral disc calcification: A no touch lesion
title_fullStr Pediatric intervertebral disc calcification: A no touch lesion
title_full_unstemmed Pediatric intervertebral disc calcification: A no touch lesion
title_short Pediatric intervertebral disc calcification: A no touch lesion
title_sort pediatric intervertebral disc calcification: a no touch lesion
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669470/
https://www.ncbi.nlm.nih.gov/pubmed/23741126
http://dx.doi.org/10.4103/0974-8237.110123
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