Cerebellar anaplastic astrocytoma in a teenager with Ollier Disease.

Abstract:

INTRODUCTION:Ollier Disease is a sporadic skeletal disorder with a predisposition to oncogenesis. It is estimated at around 1/100,000. We are presenting a young patient with Ollier Disease and high-grade astrocytoma. CASE REPORT:A 14-year-old, Caucasian male with Ollier Disease presented with a history of headaches, vomiting, blurred vision, and unsteady gait. Brain MRI with contrast showed a 41 x 55 mm mass in the posterior fossa with spotty enhancement, which pathology proved to be anaplastic astrocytoma. CONCLUSION:Despite the universal acceptance that Ollier Disease carries a high risk of developing malignancy there is very little in the literature about systematic screening. We recommended a cost-effective screening regime for these patients.

journal_name

J Neurooncol

authors

Walid MS,Troup EC

doi

10.1007/s11060-008-9583-8

subject

Has Abstract

pub_date

2008-08-01 00:00:00

pages

59-62

issue

1

eissn

0167-594X

issn

1573-7373

journal_volume

89

pub_type

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