Skip to main content
Advertisement

Main menu

  • Home
  • Content
    • Current Issue
    • Accepted Manuscripts
    • Article Preview
    • Past Issue Archive
    • AJNR Case Collection
    • Case of the Week Archive
    • Classic Case Archive
    • Case of the Month Archive
  • Special Collections
    • Spinal CSF Leak Articles (Jan 2020-June 2024)
    • 2024 AJNR Journal Awards
    • Most Impactful AJNR Articles
  • Multimedia
    • AJNR Podcast
    • AJNR Scantastics
    • Video Articles
  • For Authors
    • Submit a Manuscript
    • Author Policies
    • Fast publishing of Accepted Manuscripts
    • Graphical Abstract Preparation
    • Manuscript Submission Guidelines
    • Imaging Protocol Submission
    • Submit a Case for the Case Collection
  • About Us
    • About AJNR
    • Editorial Board
  • More
    • Become a Reviewer/Academy of Reviewers
    • Subscribers
    • Permissions
    • Alerts
    • Feedback
    • Advertisers
    • ASNR Home
  • Other Publications
    • ajnr

User menu

  • Alerts
  • Log in

Search

  • Advanced search
American Journal of Neuroradiology
American Journal of Neuroradiology

American Journal of Neuroradiology

ASHNR American Society of Functional Neuroradiology ASHNR American Society of Pediatric Neuroradiology ASSR
  • Alerts
  • Log in

Advanced Search

  • Home
  • Content
    • Current Issue
    • Accepted Manuscripts
    • Article Preview
    • Past Issue Archive
    • AJNR Case Collection
    • Case of the Week Archive
    • Classic Case Archive
    • Case of the Month Archive
  • Special Collections
    • Spinal CSF Leak Articles (Jan 2020-June 2024)
    • 2024 AJNR Journal Awards
    • Most Impactful AJNR Articles
  • Multimedia
    • AJNR Podcast
    • AJNR Scantastics
    • Video Articles
  • For Authors
    • Submit a Manuscript
    • Author Policies
    • Fast publishing of Accepted Manuscripts
    • Graphical Abstract Preparation
    • Manuscript Submission Guidelines
    • Imaging Protocol Submission
    • Submit a Case for the Case Collection
  • About Us
    • About AJNR
    • Editorial Board
  • More
    • Become a Reviewer/Academy of Reviewers
    • Subscribers
    • Permissions
    • Alerts
    • Feedback
    • Advertisers
    • ASNR Home
  • Follow AJNR on Twitter
  • Visit AJNR on Facebook
  • Follow AJNR on Instagram
  • Join AJNR on LinkedIn
  • RSS Feeds

Welcome to the new AJNR, Updated Hall of Fame, and more. Read the full announcements.


AJNR is seeking candidates for the position of Associate Section Editor, AJNR Case Collection. Read the full announcement.

 

Research ArticlePEDIATRIC

Tuberous Sclerosis: Differences between Cerebral and Cerebellar Cortical Tubers in a Pediatric Population

Luis Martí-Bonmatí, Francisco Menor and Rosa Dosdá
American Journal of Neuroradiology March 2000, 21 (3) 557-560;
Luis Martí-Bonmatí
aFrom the Department of Radiology (L.M.-B.), Doctor Peset University Hospital, the Magnetic Resonance Service (L.M.-B., R.D.), ATQ-Quiron Clinic, and the Department of Radiology (F.M.), La Fe Infantil Hospital, Valencia, Spain.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Francisco Menor
aFrom the Department of Radiology (L.M.-B.), Doctor Peset University Hospital, the Magnetic Resonance Service (L.M.-B., R.D.), ATQ-Quiron Clinic, and the Department of Radiology (F.M.), La Fe Infantil Hospital, Valencia, Spain.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Rosa Dosdá
aFrom the Department of Radiology (L.M.-B.), Doctor Peset University Hospital, the Magnetic Resonance Service (L.M.-B., R.D.), ATQ-Quiron Clinic, and the Department of Radiology (F.M.), La Fe Infantil Hospital, Valencia, Spain.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & Data
  • Info & Metrics
  • Responses
  • References
  • PDF
Loading

Abstract

BACKGROUND AND PURPOSE: Histologic evidence of cortical tubers is pathognomonic of tuberous sclerosis (TS) disease. Cerebellar tubers, however, are uncommonly found. Our objective was to evaluate the prevalence and characteristics of cerebellar tubers in a large series of pediatric patients with TS studied with MR imaging. In particular, their relationship with volume loss and age will be analyzed.

METHODS: MR images of 34 children with TS and cortical tubers were reviewed. There were 17 female and 17 male patients. The mean age was 8.9 ± 4.5 years (mean ± SD), with a range from 2 to 14 years. The number and location (supratentorial, infratentorial) of tubers and volume loss of the underlying parenchyma were recorded. The relationship between tuber location, patient age, and number of tubers was studied using the Student's t test for independent samples. The relationship between tuber location and presence of volume loss was established using the Pearson χ2 test.

RESULTS: The mean number of cortical tubers was 14.3 ± 8.5. Fifteen (44.1%) patients had cerebellar tubers associated with cerebral lesions. Patients with cerebellar and cerebral tubers had significantly more global cortical lesions than did patients with isolated cerebral tubers (17.9 ± 8.9 versus 11.4 ± 7.2 tubers, P = .026). Patients with cerebellar tubers were significantly older than those with isolated supratentorial tubers (11.3 ± 3.4 versus 7.1 ± 4.4 years, P = .005). In only four (11.8%) patients were tubers associated with focal parenchymal volume loss. The tubers in all of these cases were located in the cerebellum—indicating a significant relationship with volume loss (Pearson χ2 test, P = .017).

CONCLUSION: In this series, cerebellar tubers were frequent and were always present in association with cerebral cortical tubers. They were seen in older children with a larger total number of tubers. Cerebellar tubers may be associated with focal volume loss.

Tuberous sclerosis (TS) is a congenital neurocutaneous syndrome with variable expression in multiple organs. The most frequently involved organs are the skin, brain, retina, lungs, heart, skeleton, and kidneys. In the brain, histologic evidence of cortical tubers is pathognomonic of the disease. The tubers are characterized by disruption of normal cortical lamination, replacement of some neurons by giant cells of bizarre shape, and increased number of astrocytic nuclei (1, 2). Cells in these tubers have a divergent glioneuronal differentiation (3). The radiologic confirmation of brain tubers is considered a secondary feature of the entity (4, 5).

Tubers appear as cortical lesions that are hyperintense on proton density–weighted and T2-weighted images and hypointense on T1-weighted images (6–11). The increased signal intensity of cortical tubers often extends into the depths of the involved gyri and toward the deep white matter. The subcortical white matter close to the tubers usually shows hyperintense changes on proton density–and T2-weighted images because of gliosis and hypomyelination (1). Cerebral cortical tubers can expand the gyri. The appearance of cerebellar tubers is similar to that of their cerebral counterpart. We noticed, however, that cerebellar tubers were occasionally associated with focal volume loss and were present in older children (11).

Our objective was to evaluate the prevalence and characteristics of cerebellar tubers in a large pediatric series of patients with TS. In particular, their relationship with volume loss and age is herein analyzed.

Methods

MR images of 36 consecutive children with an established diagnosis of TS were retrospectively reviewed. For all patients, an evaluation was made of the presence and appearance of cortical cerebral and cerebellar tubers. Cortical tubers were encountered in 34 children. Therefore, two children without tubers were excluded from analysis. There were 17 female and 17 male patients. The mean age was 8.9 ± 4.5 years (mean ± SD), with a range from 2 to 14 years.

MR studies were conducted in all cases with a 0.5-T superconductive magnet. Images were obtained in the sagittal plane with a spin-echo T1-weighted short-TR short-TE sequence (550/30/2 [TR/TE/excitations]) and in the transverse plane with a spin-echo proton density–weighted and T2-weighted double-echo sequence (2200–2500/50,100/2). Sometimes, additional short time inversion recovery (1500/100/44/2 [TR/TI/TE/excitations]), gradient-echo T2*-weighted (900/28/1 with 17°), and contrast-enhanced spin-echo T1-weighted (350/30/2) sequences were also obtained. In all sequences, the section thickness was 7 mm, with an acquisition matrix of 256 × 192.

The number of tubers, location (supratentorial, infratentorial), and volume loss of the underlying parenchyma were recorded. Variables were read by two radiologists in consensus. The relationship between tuber location, patient age, and number of tubers was studied using the Student's t test for independent samples. When appropriate, data will be expressed as the mean ± SD. The relationship between tuber location and presence of volume loss was established using the Pearson χ2 test.

Results

Cortical tubers were clearly detected on proton density–and T2-weighted images as hyperintense lesions situated in the cortex of either the cerebrum or the cerebellum (Figs 1–3). Most of these lesions remained undetectable on the T1-weighted spin-echo sequences, unless they became very hypointense (four cases). In our series of 34 patients with brain tubers, 19 had isolated cerebral tubers (55.9%) and 15 had associated cerebellar tubers (44.1%). None of the patients had isolated cerebellar tubers.

fig 1.
  • Download figure
  • Open in new tab
  • Download powerpoint
fig 1.

Images from the case of a 9-year-old male patient.

A, Proton density–weighted transverse spin-echo MR image (2200/50/2) shows a right cerebellar tuber.

B, T2-weighted transverse spin-echo MR image (2200/100/2). There were 30 cerebral tubers, seven subependymal nodules, and five white matter lesions.

The total number of cortical tubers was highly variable between patients. The mean number of tubers was 14.3 ± 8.5, with a range from 1 to 30. Patients with cerebellar and cerebral tubers had more global cortical lesions than did patients with isolated cerebral tubers (17.9 ± 8.9 versus 11.4 ± 7.2 tubers). This difference was statistically significant (Student's t test, P = .026).

Patients with cerebellar tubers were older than those with isolated supratentorial tubers (11.3 ± 3.4 versus 7.1 ± 4.4 years). The difference was statistically significant (Student's t test, P = .005).

In only four patients were cortical tubers associated with parenchymal volume loss (Fig 3). In all of these cases, the tubers were located in the cerebellum. The relationship between cerebellar tubers and focal associated atrophy was statistically significant (Pearson χ2 test, P = .017). None of the supratentorial tubers had associated focal atrophy, whereas five cerebral cortical tubers had clear enlargement of the gyri.

Discussion

Cortical tubers are very frequently detected by MR imaging in patients with TS. Cortical tubers are hyperintense on proton density–weighted spin-echo, T2-weighted spin-echo, and short time inversion recovery images, remaining usually undetectable on short-TR/TE images (8, 9). In our series of 36 pediatric patients, 94.4% had brain tubers, a prevalence similar to those reported in other series (9, 12). Usually, tubers are located in the supratentorial cerebral parenchyma. Cerebellum lesions are less frequently found. We observed cerebellar tuberomas in 44.1% of our patients. In other series (7, 9, 10, 12), the frequency of cerebellar tubers was lower (between 12 and 15.8%). As in other reports (9, 12), isolatd cerebellar tubers were not found in our series. Therefore, isolated cerebellar involvement must be considered distinctly uncommon.

In our series, patients with cerebellar tubers differ from those with isolated cerebral lesions. They seem to be always associated with supratentorial tubers. We also found that patients with cerebellar tubers have more brain tubers than patients with isolated cerebral lesions. The relationship between the number of brain tubers and the presence of cerebellar lesions has not been previously studied. Because the number of cortical tubers is a biomarker of neurologic severity of cerebral dysfunction, measured by seizure status and its control and by developmental status and level of mental retardation (13), patients with cortical tubers may have more severe cerebral disease. It is well known, however, that patients with a large number of tubers do not inevitably have poor mental development. Because our study was retrospective, no attempt was made to correlate tuber location with clinical symptoms.

Additionally, patients with cerebellar tubers were older than those with isolated cerebral tubers. It is well known that TS has a variable pathologic expression in multiple organs, usually showing a chronological pattern of presentation. In this sense, cardiac rhabdomyoma detection is typically neonatal (14), the hypomelanotic maculas often occur before the age of 1 year, and renal involvement begins in infancy (15); however, ocular and other abdominal lesions are usually diagnosed when the patient is approximately 2 to 3 years of age.

The association of cerebellar tubers and focal volume loss has been reported in the literature (9, 11). In our pediatric series, focal atrophy was associated with cerebellar tubers (Fig 3) but not with cerebral tubers. This volume loss is probably related to dense gliotic tissue of glial processes histologically seen between the cellular elements (2). It is also in this gliotic matrix where calcification occurs. As previously noted, cerebellar tubers had a great tendency to calcify (7, 11). Therefore, gliosis of the cerebellar tubers must be related to both the calcification (Fig 2) and the atrophy (Fig 3) that is frequently observed in these lesions. Even more, necrosis, hemorrhage, and cellular degeneration within the tubers are exceptional.

fig 2.
  • Download figure
  • Open in new tab
  • Download powerpoint
fig 2.

Images from the case of an 11-year-old female patient.

A, Proton density–weighted transverse spin-echo MR image (2200/50/2) shows a left cerebellar tuber with hypointense inner lines from calcification.

B, T2-weighted transverse spin-echo MR image (2200/100/2). There were 29 associated cerebral cortical tubers, three associated subependymal nodules, and six associated white matter nodules and lines.

fig 3.
  • Download figure
  • Open in new tab
  • Download powerpoint
fig 3.

Images from the case of a 12-year-old male patient.

A, Proton density–weighted transverse spin-echo MR image (2200/50/2) shows a left cerebellar tuber with volume loss of the underlying parenchyma.

B, T2-weighted transverse spin-echo MR image (2200/100/2).

C, Contrast-enhanced T1-weighted transverse spin-echo MR image (350/30/2). There were 13 cerebral cortical tubers, eight subependymal nodules, and one white matter nodule.

In conclusion, cerebellar tubers are frequent findings (44.1% in our series) and they do not seem to occur in the absence of cerebral cortical tubers They occur in older children with a large total number of tubers. Cerebellar tubers may also be associated with focal cerebellar atrophy.

Footnotes

  • 1 Address reprint requests to Luis Martí-Bonmatí, MD, Sección de Resonancia Magnética, Servicio de Radiodiagnóstico, Hospital Universitario Doctor Peset, E-46017 Valencia, Spain.

References

  1. ↵
    Gomez MR. Updated tuberous sclerosis study in tuberous sclerosis. In: Gómez MR, ed. Tuberous Sclerosis. 2nd ed. New York: Raven Press; 1989: 139-148
  2. ↵
    Sarnat HB. Cytological nature of the cerebral lesions in tuberous sclerosis. In: Gómez MR, ed. Tuberous Sclerosis. 2nd ed. New York: Raven Press; 1989: 159-175
  3. ↵
    Hirose T, Scheithauer BW, Lopes MB, et al. Tuber and subependymal giant cell astrocytoma associated with tuberous sclerosis: an immunohistochemical, ultrastructural, and immunoelectron and microscopic study. Acta Neuropathol (Berl) 1995;90:387-399
    CrossRefPubMed
  4. ↵
    National Tuberous Sclerosis Association (NTSA). Diagnostic criteria. http://www.ntsa.org/index.pl/research/diag (25/10/98)
  5. Griffiths PD, Martland TR. Tuberous sclerosis complex: the role of neuroradiology. Neuropediatrics 1997;28:244-252
    CrossRefPubMed
  6. ↵
    Bell DG, King BF, Hattery RR, Charboneay JW, Hoffman AD, Houser OW. Imaging characteristics of tuberous sclerosis. AJNR Am J Neuroradiol 1991;156:1081-1086
  7. ↵
    Kingsley DPE, Kendall BE, Fitz R. Tuberous sclerosis: a clinicoradiological evaluation of 110 cases with particular reference to atypical presentation. Neuroradiology 1986;28:38-46
    CrossRefPubMed
  8. ↵
    Altman NR, Purser RK, Post MJD. Tuberous sclerosis: characteristics at CT and MR imaging. Radiology 1988;167:527-532
    CrossRefPubMed
  9. ↵
    Nixon JR, Houser OW, Gómez MR, Okazaki H. Cerebral tuberous sclerosis: MR imaging. Radiology 1989;170:869-873
    CrossRefPubMed
  10. Barkovich AJ. Phakomatoses. In: Pediatric Neuroimaging. Ed 1. New York: Raven Press; 1990: 123-147
  11. ↵
    Menor F, Martí-Bonmatí L, Mulas F, Poyatos C, Cortina H. Neuroimaging in tuberous sclerosis: a clinicoradiological evaluation in pediatric patients. Pediatr Radiol 1992;22:485-489
    CrossRefPubMed
  12. Braffman BH, Bilaniuk LT, Naidich TP, et al. MR imaging of tuberous sclerosis: pathogenesis of this phakomatosis, use of gadopentetate dimeglumine, and literature review. Radiology 1992;183:227-238
    CrossRefPubMed
  13. ↵
    Goodman M, Lamm SH, Engel A, Shepherd CW, Houser OW, Gomez MR. Cortical tuber count: a biomarker indicating neurologic severity of tuberous sclerosis complex. J Child Neurol 1997;12:85-90
    CrossRefPubMed
  14. ↵
    Bosi G, Lintermans JP, Pellegrino PA, Svaluto-Moreolo G, Vliers A. The natural history of cardiac rhabdomyoma with and without tuberous sclerosis. Acta Paediatr 1996;85:928-931
    CrossRefPubMed
  15. ↵
    Ewalt DH, Sheffield E, Sparagana SP, Delgado MR, Roach ES. Renal lesion growth in children with tuberous sclerosis complex. J Urol 1998;160:141-145
    CrossRefPubMed
  • Received June 8, 1999.
  • Copyright © American Society of Neuroradiology
PreviousNext
Back to top

In this issue

American Journal of Neuroradiology
Vol. 21, Issue 3
1 Mar 2000
  • Table of Contents
  • Index by author
Advertisement
Print
Download PDF
Email Article

Thank you for your interest in spreading the word on American Journal of Neuroradiology.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Tuberous Sclerosis: Differences between Cerebral and Cerebellar Cortical Tubers in a Pediatric Population
(Your Name) has sent you a message from American Journal of Neuroradiology
(Your Name) thought you would like to see the American Journal of Neuroradiology web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Cite this article
Luis Martí-Bonmatí, Francisco Menor, Rosa Dosdá
Tuberous Sclerosis: Differences between Cerebral and Cerebellar Cortical Tubers in a Pediatric Population
American Journal of Neuroradiology Mar 2000, 21 (3) 557-560;

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
0 Responses
Respond to this article
Share
Bookmark this article
Tuberous Sclerosis: Differences between Cerebral and Cerebellar Cortical Tubers in a Pediatric Population
Luis Martí-Bonmatí, Francisco Menor, Rosa Dosdá
American Journal of Neuroradiology Mar 2000, 21 (3) 557-560;
del.icio.us logo Twitter logo Facebook logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • Methods
    • Results
    • Discussion
    • Footnotes
    • References
  • Figures & Data
  • Info & Metrics
  • Responses
  • References
  • PDF

Related Articles

  • No related articles found.
  • PubMed
  • Google Scholar

Cited By...

  • MRI Characterization and Longitudinal Study of Focal Cerebellar Lesions in a Young Tuberous Sclerosis Cohort
  • Neonate With Erythema and Swelling of the Right Lower Extremity on Day 1
  • Crossref
  • Google Scholar

This article has not yet been cited by articles in journals that are participating in Crossref Cited-by Linking.

More in this TOC Section

  • MR Imaging Presentation of Intracranial Disease Associated with Langerhans Cell Histiocytosis
  • Subacute Sclerosing Panencephalitis Findings at MR Imaging, Diffusion MR Imaging, and Proton MR Spectroscopy
  • Neurologically Normal Complete Asymmetric Lumbar Spine Duplication
Show more PEDIATRIC

Similar Articles

Advertisement

Indexed Content

  • Current Issue
  • Accepted Manuscripts
  • Article Preview
  • Past Issues
  • Editorials
  • Editors Choice
  • Fellow Journal Club
  • Letters to the Editor

Cases

  • Case Collection
  • Archive - Case of the Week
  • Archive - Case of the Month
  • Archive - Classic Case

Special Collections

  • Special Collections

Resources

  • News and Updates
  • Turn around Times
  • Submit a Manuscript
  • Author Policies
  • Manuscript Submission Guidelines
  • Evidence-Based Medicine Level Guide
  • Publishing Checklists
  • Graphical Abstract Preparation
  • Imaging Protocol Submission
  • Submit a Case
  • Become a Reviewer/Academy of Reviewers
  • Get Peer Review Credit from Publons

Multimedia

  • AJNR Podcast
  • AJNR SCANtastic
  • Video Articles

About Us

  • About AJNR
  • Editorial Board
  • Not an AJNR Subscriber? Join Now
  • Alerts
  • Feedback
  • Advertise with us
  • Librarian Resources
  • Permissions
  • Terms and Conditions

American Society of Neuroradiology

  • Not an ASNR Member? Join Now

© 2025 by the American Society of Neuroradiology All rights, including for text and data mining, AI training, and similar technologies, are reserved.
Print ISSN: 0195-6108 Online ISSN: 1936-959X

Powered by HighWire