Literature DB >> 7985572

Neurofibromatosis type 1: the evolution of deep gray and white matter MR abnormalities.

T Itoh1, S Magnaldi, R M White, M B Denckla, K Hofman, S Naidu, R N Bryan.   

Abstract

PURPOSE: To investigate the evolution of deeply located high-signal-intensity abnormalities of the brain on T2-weighted MR images of patients with neurofibromatosis type 1 (NF-1).
METHODS: The study consists of two patient groups: 1) retrospective evaluation of MR scans of 24 symptomatic NF-1 patients, 10 of whom were sequentially studied, and 2) prospective MR evaluations of 20 asymptomatic NF-1 subjects from 14 families; 2 of these families were sequentially studied.
RESULTS: Deeply located, high-signal-intensity abnormalities on T2-weighted images were noted in 34 of 44 NF-1 subjects (77%). If NF-1 patients are grouped according to age, 28 of 30 subjects (93%) younger than 15 years had the lesions, whereas 4 of 7 subjects (57%) between 16 and 30 years, and 2 of 7 subjects (29%) older than 31 years had lesions. High-signal lesions in basal ganglia and brain stem were demonstrated in all decades with relatively high frequency. Lesions in the cerebellar white matter and dentate nuclei were mainly found in the patients younger than 10 years, and never found after the third decade. In 13 sequential studies (mean interval, 24 months), lesions appeared to increase in size in 3, remain unchanged in size in 2, and decrease in size in 7. One subject showed a mixed pattern of lesion size change.
CONCLUSIONS: Deeply located high-signal-intensity lesions on T2-weighted MR images are more evident in young NF-1 patients. The underlying brain abnormality, while pathologically unproved, is probably transient.

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Mesh:

Year:  1994        PMID: 7985572      PMCID: PMC8334401     

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  22 in total

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2.  Neuroimaging Findings in Children with Constitutional Mismatch Repair Deficiency Syndrome.

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4.  MR imaging of the corpus callosum in pediatric patients with neurofibromatosis type 1.

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Journal:  AJNR Am J Neuroradiol       Date:  2001-01       Impact factor: 3.825

5.  Age-related findings on MRI in neurofibromatosis type 1.

Authors:  Deepak S Gill; Shelley L Hyman; Adam Steinberg; Kathryn N North
Journal:  Pediatr Radiol       Date:  2006-08-16

Review 6.  Spectrum of intracranial incidental findings on pediatric brain magnetic resonance imaging: What clinician should know?

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7.  Diffusion tensor MR imaging in neurofibromatosis type 1: expanding the knowledge of microstructural brain abnormalities.

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Review 8.  Special issues in the management of gliomas in children with neurofibromatosis 1.

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9.  Unidentified bright objects on brain MRI in children as a diagnostic criterion for neurofibromatosis type 1.

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10.  Neurofibromatosis type 1 in childhood: correlation of MRI findings with intelligence.

Authors:  E Legius; M J Descheemaeker; J Steyaert; A Spaepen; R Vlietinck; P Casaer; P Demaerel; J P Fryns
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