Document Detail


Hypertrophic olivary degeneration after resection of a pontine cavernous malformation: a case report.
MedLine Citation:
PMID:  22470783     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We report the case of a 35 year old African American female who developed hypertrophic olivary degeneration secondary to resection of a pontine cavernous malformation. The patient initially complained of headaches and diplopia. Unenhanced computed tomography (CT) and magnetic resonance images (MRI) of the brain revealed a left pontine cavernous malformation with scattered foci of recent and remote hemorrhage. The patient subsequently underwent surgical resection of the lesion. Follow up MRI 7 months post surgery demonstrated hypertrophy and T2 signal hyperintensity in the ipsilateral inferior olivary nucleus secondary to hypertrophic olivary degeneration. Familiarity with this diagnosis and its imaging characteristics is required of the radiologist to prevent erroneous diagnoses of other pathology.
Authors:
Joseph L Gatlin; Robert Wineman; Bruce Schlakman; Razvan Buciuc; Majid Khan
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Publication Detail:
Type:  Case Reports; Journal Article     Date:  2011-03-01
Journal Detail:
Title:  Journal of radiology case reports     Volume:  5     ISSN:  1943-0922     ISO Abbreviation:  J Radiol Case Rep     Publication Date:  2011  
Date Detail:
Created Date:  2012-04-03     Completed Date:  2013-01-28     Revised Date:  2013-05-29    
Medline Journal Info:
Nlm Unique ID:  101494925     Medline TA:  J Radiol Case Rep     Country:  Unknown    
Other Details:
Languages:  eng     Pagination:  24-9     Citation Subset:  IM    
Affiliation:
Department of Radiology-division of Neuroradiology, University of Mississippi School of Medicine, Jackson, MS 39202, USA. jgatlin@umc.edu
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MeSH Terms
Descriptor/Qualifier:
Adult
Female
Hemangioma, Cavernous, Central Nervous System / pathology*,  surgery*
Humans
Hypertrophy / etiology
Magnetic Resonance Imaging
Olivary Nucleus / pathology*
Pons / pathology*,  surgery
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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