You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 55 No. 4, April 1998 TABLE OF CONTENTS
  Archives
  •  Online Features
  Original Contribution
 This Article
 •Full text
 •PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Citing articles on ISI (34)
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Topic Collections
 •Radiologic Imaging
 •Genetic Disorders
 •Neuromuscular diseases
 •Magnetic Resonance Imaging
 •Alert me on articles by topic

Magnetic Resonance Imaging Lesion Analysis in Neurofibromatosis Type 1

Francis J. DiMario, Jr, MD; Gale Ramsby, MD

Arch Neurol. 1998;55:500-505.

Objective  To define the evolution of identified high-signal brain parenchymal lesions on magnetic resonance imaging (MRI) studies in patients with neurofibromatosis type 1 (NF-1).

Design  A cohort of patients with NF-1 who underwent MRI were identified prospectively and their imaging studies analyzed.

Patients  All referred patients with NF-1 (as defined by National Institutes of Health consensus criteria), who had undergone imaging with MRI were eligible. Of 123 patients with NF-1 whose conditions were evaluated, 30 patients had undergone 59 MRIs. There were 22 males and 8 females, aged 1 to 53 years with mean age of 12.5 years. Two groups of patients were identified, those with brain lesions (WBL) and those with no brain lesions. All initial and subsequently obtained MRIs from the WBL group were analyzed and tallied for number, size, and location of lesions over serial studies.

Results  Of the 19 patients with WBL, lesions were in hemispheres in 19 patients, and in the brainstem and the cerebellum in 10 patients each, respectively. Lesions were located in the cerebellum and globus pallidus most often (87 of 129 lesions). Of the patients with WBL having serial studies, a total of 97 lesions equaling 197 units (mean, 2.03 units per lesion) were identified at initial study. Follow-up evaluation (interval, 0.5-4.5 years; mean, 2.3 years), showed a decrease in both total number of lesions (68 [-29%]) and size (132 units; mean, 1.86 units per lesion [-33%]). Importantly, brainstem lesions increased in both number (+36%) and size (+6.4%) over the same intervals in 7 of 13 patients with WBL studied serially, whereas hemispheric and cerebellar lesions were more evanescent.

Conclusions  High-signal T2 lesions on MRI in patients with NF-1 evolve over time. The evolution of the NF-1 lesion is region specific and may relate to preferential region-specific effects of the NF-1 gene product.


From the Department of Pediatrics, Division of Neurology (Dr DiMario) and Department of Radiology (Dr Ramsby), University of Connecticut Health Center, Farmington, and Connecticut Children's Medical Center, Hartford.



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

T2 hyperintensities in children with neurofibromatosis type 1 and their relationship to cognitive functioning
Hyman et al.
J. Neurol. Neurosurg. Psychiatry 2007;78:1088-1091.
ABSTRACT | FULL TEXT  

T 2-Weighted Hyperintensities (Unidentified Bright Objects) in Children With Neurofibromatosis 1: Their Impact on Cognitive Function
Goh et al.
J Child Neurol 2004;19:853-858.
ABSTRACT  

Review Article : Clinical Features and Pathobiology of Neurofibromatosis 1
Korf
J Child Neurol 2002;17:573-577.
ABSTRACT  

Prognostic factors of CNS tumours in Neurofibromatosis 1 (NF1): A retrospective study of 104 patients
Guillamo et al.
Brain 2002;126:152-160.
ABSTRACT | FULL TEXT  

Neurofibromatosis Type 1 Presenting With Hand Dystonia
Di Capua et al.
J Child Neurol 2001;16:606-608.
ABSTRACT  

Prospective Evaluation of the Brain in Asymptomatic Children with Neurofibromatosis Type 1: Relationship of Macrocephaly to T1 Relaxation Changes and Structural Brain Abnormalities
Steen et al.
Am. J. Neuroradiol. 2001;22:810-817.
ABSTRACT | FULL TEXT  

Why do benign astrocytomas become malignant in NF1?
Ruggieri and Packer
Neurology 2001;56:827-827.
FULL TEXT  

Use of ""unidentified bright objects"" on MRI for diagnosis of neurofibromatosis 1 in children
Curless et al.
Neurology 2000;55:1067-1068.
FULL TEXT  

Use of ""unidentified bright objects"" on MRI for diagnosis of neurofibromatosis 1 in children
DeBella et al.
Neurology 2000;54:1646-1651.
ABSTRACT | FULL TEXT  

Headaches in Patients With Neurofibromatosis-1
DiMario and Langshur
J Child Neurol 2000;15:235-238.
ABSTRACT  

Quantitative Morphology of the Corpus Callosum in Children With Neurofibromatosis and Attention-Deficit Hyperactivity Disorder
Kayl et al.
J Child Neurol 2000;15:90-96.
ABSTRACT  

Brain Morphometric Analysis in Neurofibromatosis 1
DiMario et al.
Arch Neurol 1999;56:1343-1346.
ABSTRACT | FULL TEXT  

Neurology and the skin
Hurko and Provost
J. Neurol. Neurosurg. Psychiatry 1999;66:417-430.
FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1998 American Medical Association. All Rights Reserved.