Rapid, de novo development of isolated intracranial rosai-dorfman disease: A case report

Isolated intracranial Rosai-Dorfman Disease is rare. Here, we describe a patient who developed an asymptomatic, right parietal RDD lesion over 18 months while being followed radiographically for another brain lesion. To our knowledge, rapid, de novo radiographic formation of isolated intracranial RD...

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Bibliographic Details
Published in:British journal of neurosurgery 2015-02, Vol.29 (1), p.82-84
Main Authors: Reynolds, Matthew R, Sweeney, Kieron J, Crilly, Shane M, Farrell, Michael, Jaffe, Elaine S, Javadpour, Mohsen
Format: Article
Language:English
Subjects:
Asymptotic methods
Knowledge
Neurosurgery
Radiography
Online Access:Get full text
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Summary:Isolated intracranial Rosai-Dorfman Disease is rare. Here, we describe a patient who developed an asymptomatic, right parietal RDD lesion over 18 months while being followed radiographically for another brain lesion. To our knowledge, rapid, de novo radiographic formation of isolated intracranial RDD has never been reported in an asymptomatic patient.
ISSN:0268-8697
1360-046X
DOI:10.3109/02688697.2014.950634