Hyperintensity of the middle cerebellar peduncles on fluid-attenuated inversion recovery imaging: variation with age and implications for the diagnosis of multiple system atrophy
- PMID: 17110685
- PMCID: PMC7977213
Hyperintensity of the middle cerebellar peduncles on fluid-attenuated inversion recovery imaging: variation with age and implications for the diagnosis of multiple system atrophy
Abstract
Background and purpose: T2 hyperintensity of the middle cerebellar peduncle (MCP) is described in a number of diseases, including multiple system atrophy (MSA). We hypothesize that mild MCP hyperintensity on fluid-attenuated inversion recovery (FLAIR) imaging can be a normal finding. To our knowledge, a detailed study of the prevalence of this finding in various age groups with the FLAIR sequence has not been described.
Methods: One hundred twenty-two patients underwent an axial FLAIR examination of the brain as part of either a hearing loss or tinnitus work-up (ie, to exclude an acoustic neuroma or a retrocochlear cause). Subjects aged 15-78 years were included to reflect an even spread through the decades and were divided into 6 age groups. A radiologist and an MR imaging fellow graded the examinations subjectively, blinded to age: 0 for normal or 1 for the presence of MCP hyperintensity if the increased signal intensity was greater than that of adjacent pons and cerebellar white matter. Spearman rank correlation test of MCP hyperintensity with age and analysis of variance (ANOVA) were performed.
Results: Of 122 patients, we identified 17 with MCP FLAIR hyperintensity. None of these patients had a clinical condition that could cause MCP hyperintensity. MCP hyperintensity did not show a statistically significant correlation with age (r = 0.05, P = .62). Patients were divided into 6 age groups, and ANOVA showed no statistically significant difference in the incidence of MCP hyperintensity between different age groups (P = .95). However, results were highly reproducible with excellent interobserver correlation (r = 0.97, P < .001).
Conclusions: Mild MCP FLAIR hyperintensity can occur normally, and this finding shows no relationship with age.
Figures
Similar articles
-
Hyperintensity of the precentral gyral subcortical white matter and hypointensity of the precentral gyrus on fluid-attenuated inversion recovery: variation with age and implications for the diagnosis of amyotrophic lateral sclerosis.AJNR Am J Neuroradiol. 2007 Feb;28(2):250-4. AJNR Am J Neuroradiol. 2007. PMID: 17296988 Free PMC article.
-
Bright middle cerebellar peduncle sign in multiple system atrophy with predominant cerebellar ataxia is more apparent in double-inversion recovery imaging than in conventional imaging.PLoS One. 2024 Nov 13;19(11):e0313651. doi: 10.1371/journal.pone.0313651. eCollection 2024. PLoS One. 2024. PMID: 39536000 Free PMC article.
-
MR imaging of middle cerebellar peduncle width: differentiation of multiple system atrophy from Parkinson disease.Radiology. 2006 Jun;239(3):825-30. doi: 10.1148/radiol.2393050459. Radiology. 2006. PMID: 16714464
-
Multiple system atrophy.Semin Neurol. 2014 Apr;34(2):174-81. doi: 10.1055/s-0034-1381737. Epub 2014 Jun 25. Semin Neurol. 2014. PMID: 24963676 Review.
-
Abnormal hyperintensity within the subarachnoid space evaluated by fluid-attenuated inversion-recovery MR imaging: a spectrum of central nervous system diseases.Eur Radiol. 2003 Dec;13 Suppl 4:L192-201. doi: 10.1007/s00330-003-1877-9. Eur Radiol. 2003. PMID: 15018187 Review.
Cited by
-
Relevance of corpus callosum splenium versus middle cerebellar peduncle hyperintensity for FXTAS diagnosis in clinical practice.J Neurol. 2015 Feb;262(2):435-42. doi: 10.1007/s00415-014-7557-7. Epub 2014 Dec 2. J Neurol. 2015. PMID: 25451852
-
Bilateral middle cerebellar peduncle lesions: Neuroimaging features and differential diagnoses.Brain Behav. 2020 Oct;10(10):e01778. doi: 10.1002/brb3.1778. Epub 2020 Aug 5. Brain Behav. 2020. PMID: 32755074 Free PMC article.
-
Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia-experience from an Italian cohort.J Neurol. 2024 Aug;271(8):5478-5488. doi: 10.1007/s00415-024-12506-x. Epub 2024 Jun 17. J Neurol. 2024. PMID: 38886208
-
Neuroimaging in Dementia.Semin Neurol. 2017 Oct;37(5):510-537. doi: 10.1055/s-0037-1608808. Epub 2017 Dec 5. Semin Neurol. 2017. PMID: 29207412 Free PMC article. Review.
-
Enlarged perivascular spaces and their association with motor, cognition, MRI markers and cerebrovascular risk factors in male fragile X premutation carriers.J Neurol Sci. 2024 Jun 15;461:123056. doi: 10.1016/j.jns.2024.123056. Epub 2024 May 17. J Neurol Sci. 2024. PMID: 38772058 Free PMC article.
References
-
- Seppi K, Schocke MF, Wenning GK, et al. How to diagnose MSA early: the role of magnetic resonance imaging. J Neural Transm 2005;112:1625–34 - PubMed
-
- Schrag A, Good CD, Miszkiel K, et al. Differentiation of atypical parkinsonian syndromes with routine MRI. Neurology 2000;55:1239–40 - PubMed
-
- Savoiardo M. Differential diagnosis of Parkinson’s disease and atypical parkinsonian disorders by magnetic resonance imaging. Neurol Sci 2003;24:S35–S37 - PubMed
-
- Lee EA, Cho HI, Kim SS, et al. Comparison of magnetic resonance imaging in subtypes of multiple system atrophy. Parkinsonism Relat Disord 2004;10:363–68 - PubMed
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous