Radiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Published online before print December 22, 2004, 10.1148/radiol.2342031497
This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
2342031497v1
234/2/535    most recent
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Habermann, C. R.
Right arrow Articles by Adam, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Habermann, C. R.
Right arrow Articles by Adam, G.
(Radiology 2005;234:535-541.)
© RSNA, 2004


Pediatric Imaging

MR Evaluation of Dural Ectasia in Marfan Syndrome: Reassessment of the Established Criteria in Children, Adolescents, and Young Adults1

Christian R. Habermann, MD, Florian Weiss, MD, Volker Schoder, MSc, Miriam C. Cramer, MD, Joern Kemper, MD, Oliver Wittkugel, MD and Gerhard Adam, MD

1 From the Department of Diagnostic and Interventional Radiology (C.R.H., F.W., M.C.C., J.K., G.A.), Institute for Medical Biometry and Epidemiology (V.S.), and Department of Neuroradiology (O.W.), University Hospital Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany. Received September 18, 2003; revision requested December 2; final revision received April 7, 2004; accepted May 26. Address correspondence to C.R.H. (e-mail: c.habermann@uke.uni-hamburg.de).

PURPOSE: To retrospectively evaluate known criteria for assessment of dural ectasia by using magnetic resonance (MR) imaging in children, adolescents, and young adults with and those without Marfan syndrome.

MATERIALS AND METHODS: Local ethics committee approval and informed consent were obtained. MR images of the lumbar spine in 28 patients with clinically proved Marfan syndrome (group A; 17 male, 11 female; age range, 4–21 years; mean, 12.1 years), seven patients with suspicion of Marfan syndrome (group B; six male, one female; age range, 6–18 years; mean, 10.4 years), and 55 patients without Marfan syndrome (group C; 26 male, 29 female; age range, 4–20 years; mean, 10.7 years) were evaluated retrospectively for dural ectasia criteria (scalloping, dural sac ratio, nerve root sleeve diameter, sagittal dural sac width at S1 greater than that at L4) and according to classifications by Ahn et al and Fattori et al. For statistical comparison of results, one-way analysis of variance with Scheffe post hoc comparisons was used, with an overall two-tailed significance at {alpha} = .05.

RESULTS: No significant differences in scalloping and nerve root sleeve diameter were shown between groups. A significant difference was measured for dural sac ratios at L5 and S1 (F test, P = .003 and P < .001 at L5 and S1, respectively; post hoc t test for groups A vs C, P = .004 and P < .001 at L5 and S1, respectively). Significant differences were also obtained between groups A and C for sagittal dural sac width at S1 greater than that at L4 according to the calculated mean difference (for both F test and post hoc t test, P < .001 and P = .003 at S1 and L4, respectively). The Ahn et al and Fattori et al classifications were of limited value.

CONCLUSION: The data suggest that only dural sac ratio at L5 and S1 and a sagittal dural sac width at S1 greater than that at L4 are statistically significant criteria for the assessment of dural ectasia in children, adolescents, and young adults.

© RSNA, 2004




This article has been cited by other articles:


Home page
PediatricsHome page
L. Faivre, A. Masurel-Paulet, G. Collod-Beroud, B. L. Callewaert, A. H. Child, C. Stheneur, C. Binquet, E. Gautier, B. Chevallier, F. Huet, et al.
Clinical and Molecular Study of 320 Children With Marfan Syndrome and Related Type I Fibrillinopathies in a Series of 1009 Probands With Pathogenic FBN1 Mutations
Pediatrics, January 1, 2009; 123(1): 391 - 398.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
I. Sanchez, L. Concepcion, J. J. Cortes, and C. Pack
Dural ectasia in Marfan syndrome
Neurology, October 21, 2008; 71(17): 1378 - 1378.
[Full Text] [PDF]


Home page
JBJSHome page
R. L. Ferguson
Medical and Congenital Comorbidities Associated with Spinal Deformities in the Immature Spine
J. Bone Joint Surg. Am., February 1, 2007; 89(suppl_1): 34 - 41.
[Full Text] [PDF]


Home page
radtechHome page
J. A. CHAFFINS
Marfan Syndrome
Radiol. Technol., January 1, 2007; 78(3): 222 - 236.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
RADIOLOGY RADIOGRAPHICS RSNA JOURNALS ONLINE
Copyright © 2005 by the Radiological Society of North America.