Literature DB >> 7931583

Terminal syringohydromyelia and occult spinal dysraphism.

B J Iskandar1, W J Oakes, C McLaughlin, A K Osumi, R D Tien.   

Abstract

Terminal syringohydromyelia is a cystic dilatation of the lower third of the spinal cord. The authors describe its incidence and characteristics, its frequent association with occult spinal dysraphism, and its clinical significance and need for surgical treatment. All 143 cases of occult spinal dysraphism treated at the Duke University Medical Center between 1972 and 1992 were reviewed. A terminal syrinx was found in 24 (27%) of the 90 cases that were evaluated by magnetic resonance (MR) imaging. In contrast three (6.2%) of 48 cases evaluated by myelography and postmyelographic computerized tomography had a syrinx documented. The relative radiographic severity of the different syringes was estimated by using measurements of the syrinx and spinal cord on the MR images, classifying the cysts into large and small. Large syringes were frequently symptomatic, commonly presenting with pain, motor and sensory deficits of the lower extremities, scoliosis, and bowel and bladder dysfunction. Terminal syringohydromyelia with occult spinal dysraphic lesions was most often associated with tethered spinal cord from a tight filum terminale in the presence of an anorectal anomaly (67% of cases), meningocele manqué (54%), and diastematomyelia (38%). An infrequent association was seen with other spinal cord anomalies. The results of surgical management of terminal syringohydromyelia were analyzed, highlighting the necessity and effectiveness of shunting the large cysts, especially in the setting of a progressive symptomatology. Of the 11 patients with shunts who underwent MR imaging, 10 showed either complete or significant resolution of the syrinx; all five patients who had presented with pain (mainly back pain) showed complete resolution of the pain after shunting; finally, one-third of patients with shunt placement had significant postoperative improvement in their neurological examination, whereas none worsened. It is stressed that terminal syringohydromyelia is an important pathological entity that should be considered in patients with occult spinal dysraphism, and treated surgically when clinically or radiographically significant.

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Year:  1994        PMID: 7931583     DOI: 10.3171/jns.1994.81.4.0513

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  15 in total

1.  The value of postoperative MR in tethered cord: a review of 140 cases.

Authors:  P David Halevi; Suhas Udayakumaran; Liat Ben-Sira; Shlomi Constantini
Journal:  Childs Nerv Syst       Date:  2011-09-29       Impact factor: 1.475

Review 2.  Holocord syringomyelia secondary to tethered spinal cord associated with anterior sacral meningocele and tailgut cyst: case report and review of literature.

Authors:  Joanna Kemp; Miguel A Guzman; Colleen M Fitzpatrick; Samer K Elbabaa
Journal:  Childs Nerv Syst       Date:  2014-02-22       Impact factor: 1.475

Review 3.  Meningocele manqué: a comprehensive review of this enigmatic finding in occult spinal dysraphism.

Authors:  Cameron Schmidt; Ellie Bryant; Joe Iwanaga; Rod J Oskouian; W Jerry Oakes; R Shane Tubbs
Journal:  Childs Nerv Syst       Date:  2017-06-15       Impact factor: 1.475

Review 4.  Syringomyelia and tethered cord in children.

Authors:  Vasilios Tsitouras; Spyros Sgouros
Journal:  Childs Nerv Syst       Date:  2013-09-07       Impact factor: 1.475

5.  Diastematomyelia in children: treatment outcome and natural history of associated syringomyelia.

Authors:  Y C Gan; S Sgouros; A R Walsh; A D Hockley
Journal:  Childs Nerv Syst       Date:  2006-10-07       Impact factor: 1.475

6.  Familial Chiari type I malformation with syringomyelia in two siblings: case report and review of the literature.

Authors:  Gaurav G Mavinkurve; Daniel Sciubba; Eric Amundson; George I Jallo
Journal:  Childs Nerv Syst       Date:  2005-04-09       Impact factor: 1.475

7.  Syringo-subarachnoidal shunting to correct unilateral leg deformity in a child with terminal syringomyelia: case report.

Authors:  Takeshi Aoyama; Masafumi Ohtaki; Izumi Koyanagi; Maiko Kawamura; Masahiko Chiba
Journal:  Childs Nerv Syst       Date:  2008-03-20       Impact factor: 1.475

Review 8.  Multiple coexistent dysraphic pathologies.

Authors:  Guirish A Solanki; James Evans; Andrew Copp; Dominic N P Thompson
Journal:  Childs Nerv Syst       Date:  2003-04-12       Impact factor: 1.475

9.  An international collaborative family-based whole-genome linkage scan for high-grade myopia.

Authors:  Yi-Ju Li; Jeremy A Guggenheim; Anuradha Bulusu; Ravikanth Metlapally; Diana Abbott; Francois Malecaze; Patrick Calvas; Thomas Rosenberg; Sandrine Paget; Rosalind C Creer; George Kirov; Michael J Owen; Bei Zhao; Tristan White; David A Mackey; Terri L Young
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-03-25       Impact factor: 4.799

10.  Asymptomatic lumbosacral lipomas--a natural history study.

Authors:  Victoria Wykes; Divyesh Desai; Dominic N P Thompson
Journal:  Childs Nerv Syst       Date:  2012-05-05       Impact factor: 1.475

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