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Split cord malformation – A study of 300 cases at AIIMS 1990–2006

BACKGROUND: Split cord malformation (SCM) is a rare condition. With decreasing incidence of neural tube defect (NTD) in the West, the reports of SCM are getting lesser and lesser. However, in India, spinal dysraphism is still a major problem encountered by the neurosurgeons. OBJECTIVE: Our aim was t...

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Autor principal: Mahapatra, A. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3208912/
https://www.ncbi.nlm.nih.gov/pubmed/22069430
http://dx.doi.org/10.4103/1817-1745.85708
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author Mahapatra, A. K.
author_facet Mahapatra, A. K.
author_sort Mahapatra, A. K.
collection PubMed
description BACKGROUND: Split cord malformation (SCM) is a rare condition. With decreasing incidence of neural tube defect (NTD) in the West, the reports of SCM are getting lesser and lesser. However, in India, spinal dysraphism is still a major problem encountered by the neurosurgeons. OBJECTIVE: Our aim was to analyze 300 patients of SCM for their clinical features, radiological findings and outcome of surgery, which can throw light on the subject to others, who have less scope of finding these cases frequently. MATERIALS AND METHODS: Over a 16-year period, we encountered 300 cases of SCM at AIIMS. Over the same period, more than 1500 cases of NTD were managed. SCM was noticed in 20% of cases with NTD. Skin stigmata were noted in two-third of the cases, and scoliosis and foot deformity were observed in 50% and 48% cases, respectively. Motor and sensory deficits were observed in 80% and 70% cases, respectively. Commonest site affected was lumbar or dorsolumbar (55% and 23%, respectively). In 3% cases, it was cervical in location. Magnetic resonance imaging (MRI) scan revealed a large number of anomalies like lipoma, neuroenteric cyst, thick filum and dermoid or epidermoid cysts. All the patients were surgically treated. In type I, bony spurs were excised, and in type II, bands tethering the cord were released. Associated anomalies were managed in the same sitting. Patients were followed up from 3 months to 3 years. RESULTS: Overall improvement was noticed in 50% and stabilization in 44% cases and deterioration of neurological status was recorded in 6% cases. However, 50% of those who deteriorated improved to preop status prior to discharge, 7-10 days following surgery. CONCLUSIONS: SCM is rare and not many large series are available. We operated 300 cases and noticed a large number of associated anomalies and also multilevel and multisite splits. Improvement or stabilization was noted in 94% and deterioration in 6% cases. We recommended prophylactic surgery for our asymptomatic patients.
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spelling pubmed-32089122011-11-08 Split cord malformation – A study of 300 cases at AIIMS 1990–2006 Mahapatra, A. K. J Pediatr Neurosci Original Article BACKGROUND: Split cord malformation (SCM) is a rare condition. With decreasing incidence of neural tube defect (NTD) in the West, the reports of SCM are getting lesser and lesser. However, in India, spinal dysraphism is still a major problem encountered by the neurosurgeons. OBJECTIVE: Our aim was to analyze 300 patients of SCM for their clinical features, radiological findings and outcome of surgery, which can throw light on the subject to others, who have less scope of finding these cases frequently. MATERIALS AND METHODS: Over a 16-year period, we encountered 300 cases of SCM at AIIMS. Over the same period, more than 1500 cases of NTD were managed. SCM was noticed in 20% of cases with NTD. Skin stigmata were noted in two-third of the cases, and scoliosis and foot deformity were observed in 50% and 48% cases, respectively. Motor and sensory deficits were observed in 80% and 70% cases, respectively. Commonest site affected was lumbar or dorsolumbar (55% and 23%, respectively). In 3% cases, it was cervical in location. Magnetic resonance imaging (MRI) scan revealed a large number of anomalies like lipoma, neuroenteric cyst, thick filum and dermoid or epidermoid cysts. All the patients were surgically treated. In type I, bony spurs were excised, and in type II, bands tethering the cord were released. Associated anomalies were managed in the same sitting. Patients were followed up from 3 months to 3 years. RESULTS: Overall improvement was noticed in 50% and stabilization in 44% cases and deterioration of neurological status was recorded in 6% cases. However, 50% of those who deteriorated improved to preop status prior to discharge, 7-10 days following surgery. CONCLUSIONS: SCM is rare and not many large series are available. We operated 300 cases and noticed a large number of associated anomalies and also multilevel and multisite splits. Improvement or stabilization was noted in 94% and deterioration in 6% cases. We recommended prophylactic surgery for our asymptomatic patients. Medknow Publications 2011-10 /pmc/articles/PMC3208912/ /pubmed/22069430 http://dx.doi.org/10.4103/1817-1745.85708 Text en Copyright: © Journal of Pediatric Neurosciences 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 Original Article
Mahapatra, A. K.
Split cord malformation – A study of 300 cases at AIIMS 1990–2006
title Split cord malformation – A study of 300 cases at AIIMS 1990–2006
title_full Split cord malformation – A study of 300 cases at AIIMS 1990–2006
title_fullStr Split cord malformation – A study of 300 cases at AIIMS 1990–2006
title_full_unstemmed Split cord malformation – A study of 300 cases at AIIMS 1990–2006
title_short Split cord malformation – A study of 300 cases at AIIMS 1990–2006
title_sort split cord malformation – a study of 300 cases at aiims 1990–2006
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3208912/
https://www.ncbi.nlm.nih.gov/pubmed/22069430
http://dx.doi.org/10.4103/1817-1745.85708
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