Literature DB >> 1407429

Split cord malformation: Part II: Clinical syndrome.

D Pang1.   

Abstract

Thirty-nine patients with split cord malformations (SCM) were studied in detail with respect to their clinical, radiographic, and surgical findings as well as their outcome data. Eight patients were adults and 31 patients were children. According to the classification endorsed by Part I of the SCM study, 19 patients had Type I SCM (6 adults and 13 children), 18 patients had Type II SCM (2 adults and 16 children), and 2 patients had composite SCM with both lesion types situated in tandem. Six SCMs were cervical, 2 were thoracic, and 31 were in the lumbar region. All 8 adults had pain and progressive sensorimotor deficits at diagnosis. Only 16 of the 31 children had symptoms, and among these, 14 had progressive sensorimotor deficits, but only 6 had pain. The difference in the clinical picture between adults and children is similar to that described in the tethered cord syndrome, except for left-right functional discrepancy, which was prominent in 8 children with SCM but rarely seen in tethered cord syndrome due to other causes. Cutaneous manifestations of either occult or open dysraphic states were present in all but 3 patients; hypertrichosis was by far the best predictor of an underlying SCM, being found in 56% in the series. Neurological deterioration in SCM was independent of the lesion type: the Type I:Type II ratio for symptomatic progression was 13:11. It was also independent of the location of the lesion: 67% of patients with cervical SCMs had symptomatic progression versus 64% of patients with thoracolumbar lesions. High-resolution, thin cut, axial computed tomographic myelography using bone algorithms was more sensitive than magnetic resonance imaging in defining the anatomical details of the SCM. Radiographic classifications of the SCM, using the nature of the median septum and the number of dural tubes as criteria, was always possible without ambiguity. However, whereas every Type I bone septum was identified preoperatively, only 5 Type II fibrous septa were revealed by preoperative imaging, even though a fibrous septum and/or other fibroneurovascular bands were found tethering the hemicords in every Type II case at surgery. Complete imaging studies also showed that all lumbar SCMs had low-lying coni and at least one additional tethering lesion besides the split cords, whereas only 1 of 7 cervical and high thoracic SCMs had a low conus and a second tethering lesion. The surgical goal for SCM was release of the tethered hemicords by eliminating the bone spurs, dural sleeves, fibrous septa, or any fibroneurovascular bands (myelomeningoceles manqué) that might be transfixing the split cord. Type I cases were technically more difficult and had a slightly higher surgical morbidity than Type II cases, especially if an oblique bone septum had asymmetrically divided the cord into one larger hemicord and one smaller, hence, very delicate, hemicord.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1992        PMID: 1407429     DOI: 10.1227/00006123-199209000-00011

Source DB:  PubMed          Journal:  Neurosurgery        ISSN: 0148-396X            Impact factor:   4.654


  64 in total

1.  Composite type of split cord malformations.

Authors:  Yusuf Erşahin
Journal:  Childs Nerv Syst       Date:  2002-01-18       Impact factor: 1.475

Review 2.  Split spinal cord malformations: report of 22 cases and review of the literature.

Authors:  Edgardo Schijman
Journal:  Childs Nerv Syst       Date:  2003-02-05       Impact factor: 1.475

Review 3.  Sonographic spinal imaging of normal anatomy, pathology and magnetic growing rods in children.

Authors:  Arthur B Meyers; Tushar Chandra; Monica Epelman
Journal:  Pediatr Radiol       Date:  2017-08-04

Review 4.  Congenital spine anomalies: the closed spinal dysraphisms.

Authors:  Erin Simon Schwartz; Andrea Rossi
Journal:  Pediatr Radiol       Date:  2015-09-07

5.  Hemimyeloschisis associated with hydrocephalus.

Authors:  Yusuf Izci
Journal:  Childs Nerv Syst       Date:  2015-11-25       Impact factor: 1.475

6.  An unusual sequelae of an infected persistent dermal sinus tract.

Authors:  R Shane Tubbs; Philip K Frykman; Carroll M Harmon; W Jerry Oakes; John C Wellons
Journal:  Childs Nerv Syst       Date:  2006-08-30       Impact factor: 1.475

7.  An unusual case of split cord malformation.

Authors:  J Moriya; S Kakeda; Y Korogi; Y Soejima; E Urasaki; A Yokota
Journal:  AJNR Am J Neuroradiol       Date:  2006-08       Impact factor: 3.825

8.  A case of split cord malformation associated with myeloschisis.

Authors:  Katsuhiko Akiyama; Kenichi Nishiyama; Junichi Yoshimura; Hiroshi Mori; Yukihiko Fujii
Journal:  Childs Nerv Syst       Date:  2006-10-07       Impact factor: 1.475

9.  Comparative study of complex spina bifida and split cord malformation.

Authors:  Raj Kumar; S N Singh; K K Bansal; Vinita Singh
Journal:  Indian J Pediatr       Date:  2005-02       Impact factor: 1.967

10.  Prenatal diagnosis of diastematomyelia.

Authors:  Pascale Sonigo-Cohen; Pierre Schmit; Michel Zerah; Latifa Chat; Isabelle Simon; Marie Cécile Aubry; Marie Gonzales; Alain Pierre-Kahn; Francis Brunelle
Journal:  Childs Nerv Syst       Date:  2003-07-04       Impact factor: 1.475

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