Medulloblastoma mimicking Lhermitte-Duclos disease on MRI and CT

Annette C. Douglas-Akinwande, Troy D. Payner, Eyas M. Hattab

Research output: Contribution to journalArticlepeer-review

21 Scopus citations


Background: Although previous reports purport that the unique magnetic resonance imaging (MRI) features of Lhermitte-Duclos disease (LDD) obviates the need for biopsy, medulloblastoma can have an indistinguishable imaging appearance. Case description: We present a patient who suffered from a medulloblastoma that demonstrated no enhancement and had imaging characteristics that were indistinguishable from LDD. This atypical imaging appearance, which could potentially be confused with LDD, may lead to misdiagnosis and inappropriate treatment in the absence of tissue sampling. Conclusion: In those patients where imaging is highly suggestive of LDD but lack other manifestations of Cowden syndrome, biopsy is required and advanced imaging with magnetic resonance spectroscopy (MRS) should be strongly considered.

Original languageEnglish (US)
Pages (from-to)536-539
Number of pages4
JournalClinical Neurology and Neurosurgery
Issue number6
StatePublished - Jul 1 2009


  • Imaging
  • Lhermitte-Duclos disease
  • Medulloblastoma

ASJC Scopus subject areas

  • Clinical Neurology
  • Surgery

Fingerprint Dive into the research topics of 'Medulloblastoma mimicking Lhermitte-Duclos disease on MRI and CT'. Together they form a unique fingerprint.

Cite this