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Split notochord syndrome associated with dorsal neuroenteric fistula: A rare entity

Split notochord syndrome (SNS) is an extremely rare congenital malformation associated with anomalies of the vertebral column, gastrointestinal tract and central nervous system. Twenty cases of SNS associated with dorsal enteric fistula have been reported in literature till date. The present report...

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Autores principales: Srivastava, Punit, Gangopadhyay, A. N., Gupta, D. K., Sharma, S. P.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3087992/
https://www.ncbi.nlm.nih.gov/pubmed/21559161
http://dx.doi.org/10.4103/1817-1745.76112
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author Srivastava, Punit
Gangopadhyay, A. N.
Gupta, D. K.
Sharma, S. P.
author_facet Srivastava, Punit
Gangopadhyay, A. N.
Gupta, D. K.
Sharma, S. P.
author_sort Srivastava, Punit
collection PubMed
description Split notochord syndrome (SNS) is an extremely rare congenital malformation associated with anomalies of the vertebral column, gastrointestinal tract and central nervous system. Twenty cases of SNS associated with dorsal enteric fistula have been reported in literature till date. The present report describes a unique case of SNS associated with lumbosacral meningomyelocele, dorsal neuroenteric fistula and dorsal herniation of right kidney along with vessels. The neonate was well managed by excision of enteric fistula, closure of duramater of meningomyelocele and repair of posterior wall hernia after placement of kidney in renal fossa. This kind of entity is uncommon and not been reported earlier.
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spelling pubmed-30879922011-05-10 Split notochord syndrome associated with dorsal neuroenteric fistula: A rare entity Srivastava, Punit Gangopadhyay, A. N. Gupta, D. K. Sharma, S. P. J Pediatr Neurosci Case Report Split notochord syndrome (SNS) is an extremely rare congenital malformation associated with anomalies of the vertebral column, gastrointestinal tract and central nervous system. Twenty cases of SNS associated with dorsal enteric fistula have been reported in literature till date. The present report describes a unique case of SNS associated with lumbosacral meningomyelocele, dorsal neuroenteric fistula and dorsal herniation of right kidney along with vessels. The neonate was well managed by excision of enteric fistula, closure of duramater of meningomyelocele and repair of posterior wall hernia after placement of kidney in renal fossa. This kind of entity is uncommon and not been reported earlier. Medknow Publications 2010 /pmc/articles/PMC3087992/ /pubmed/21559161 http://dx.doi.org/10.4103/1817-1745.76112 Text en © Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Srivastava, Punit
Gangopadhyay, A. N.
Gupta, D. K.
Sharma, S. P.
Split notochord syndrome associated with dorsal neuroenteric fistula: A rare entity
title Split notochord syndrome associated with dorsal neuroenteric fistula: A rare entity
title_full Split notochord syndrome associated with dorsal neuroenteric fistula: A rare entity
title_fullStr Split notochord syndrome associated with dorsal neuroenteric fistula: A rare entity
title_full_unstemmed Split notochord syndrome associated with dorsal neuroenteric fistula: A rare entity
title_short Split notochord syndrome associated with dorsal neuroenteric fistula: A rare entity
title_sort split notochord syndrome associated with dorsal neuroenteric fistula: a rare entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3087992/
https://www.ncbi.nlm.nih.gov/pubmed/21559161
http://dx.doi.org/10.4103/1817-1745.76112
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