A 70-year-old woman presented with a 3-week history of progressive left hemichorea-hemiballism. Based on elevated serum glucose (384 mg/dL) and HbA1c (13.2%) plus neuroimaging findings (figure, A and B), she was diagnosed with hyperglycemia-induced hemichorea-hemiballism.1 She was treated with insulin and risperidone with near resolution after 4 days. Additional neuroimaging (figure, C and D) revealed a developmental venous anomaly (DVA) adjacent to the affected putamen. The DVA was associated with increased cerebral blood flow and volume2 (figure, E and F). DVAs are typically asymptomatic. However, we propose that altered hemodynamics within the basal ganglia together with this patient's metabolic disturbance resulted in the movement disorder: a 2-hit hypothesis.
The right putamen is hyperdense on CT head (A) and hyperintense on T1-weighted MRI brain (B) which is classic for hyperglycemia-induced hemichorea-hemiballism. The characteristic caput medusa of a developmental venous anomaly (arrowheads) is seen on CT head with contrast (C) and gadolinium-enhanced 3T MRI brain (D). CT perfusion demonstrates increased cerebral blood flow (E) and increased cerebral blood volume (F) in the affected putamen (arrows).
Acknowledgments
Acknowledgment: The authors thank the patient for contributing her time to this case study.
Footnotes
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Study funding: L.V.K. is supported by a Canadian Health Institutes of Research (CIHR) Clinician-Scientist Award. M.M. receives operating funds from a Parkinson Society Canada New Investigator Award and is funded by the Department of Medicine, Sunnybrook Health Sciences Centre.
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Author contributions: Dr. Kalia conceived and designed the study, analyzed and interpreted the data, and drafted and revised the manuscript. Dr. Mozessohn contributed to design of the study and to revision of the manuscript. Dr. Aviv contributed to analysis and interpretation of the data and to revision of the manuscript. Dr. Da Costa contributed to revision of the manuscript. Dr. Lang contributed to design of the study and to revision of the manuscript. Dr. Shadowitz contributed to design of the study and to revision of the manuscript. Dr. Masellis conceived and designed the study, analyzed and interpreted the data, and drafted and revised the manuscript.
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Disclosure: Dr. Kalia is funded by a Clinician-Scientist Phase I Award from the CIHR. Dr. Mozessohn, Dr. Aviv, and Dr. Da Costa report no disclosures. Dr. Lang has served on scientific advisory boards for Abbott, Allon Therapeutics, Inc., Biovail Corporation, Boehringer Ingelheim, Cephalon, Inc., Ceregene, Eisai Inc., Medtronic, Inc., Lundbeck Inc., NeuroMolecular Pharmaceuticals, Novartis, Merck Serono, Solvay Pharmaceuticals, Inc., TaroPharma, and Teva Pharmaceutical Industries Ltd.; has received speaker honoraria from GlaxoSmithKline and UCB; receives/has received research support from the CIHR, the Dystonia Medical Research Foundation, the Michael J. Fox Foundation, the National Parkinson Foundation, and the Ontario Problem Gambling Research Centre; and has served as an expert witness in cases related to the welding industry. Dr. Shadowitz reports no disclosures. Dr. Masellis serves as CME lecturer for and has received speaker honoraria from Novartis and EMD Serono, Inc.; serves as an Associate Editor for Current Pharmacogenomics and Personalized Medicine; has received publishing royalties from Henry Stewart Talks; serves as a consultant for Bioscape Medical Imaging CRO; and receives research support from Novartis, a CIHR Clinician Scientist Award, the Department of Medicine, Sunnybrook Health Sciences Centre, a Parkinson Society Canada New Investigator Award.
- Copyright © 2012 by AAN Enterprises, Inc.
Disputes & Debates: Rapid online correspondence
- Response to Drs. Civardi and Collini
- Putaminal CT hyperperfusion in hyperkinetic disorders
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