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April 30, 2013; 80 (18) NeuroImages

Holohemispheric developmental venous anomaly

Andrew K. Jung, John W. Henson, Daniel Susanto, Lisa M. Caylor, Michael J. Doherty
First published April 29, 2013, DOI: https://doi.org/10.1212/WNL.0b013e3182904fbb
Andrew K. Jung
From the Zanvyl Krieger School of Arts and Sciences (A.K.J.), Johns Hopkins University, Baltimore, MD; and Swedish Neuroscience Institute (J.W.H., D.S., L.M.C., M.J.D.), Seattle, WA.
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John W. Henson
From the Zanvyl Krieger School of Arts and Sciences (A.K.J.), Johns Hopkins University, Baltimore, MD; and Swedish Neuroscience Institute (J.W.H., D.S., L.M.C., M.J.D.), Seattle, WA.
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Daniel Susanto
From the Zanvyl Krieger School of Arts and Sciences (A.K.J.), Johns Hopkins University, Baltimore, MD; and Swedish Neuroscience Institute (J.W.H., D.S., L.M.C., M.J.D.), Seattle, WA.
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Lisa M. Caylor
From the Zanvyl Krieger School of Arts and Sciences (A.K.J.), Johns Hopkins University, Baltimore, MD; and Swedish Neuroscience Institute (J.W.H., D.S., L.M.C., M.J.D.), Seattle, WA.
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Michael J. Doherty
From the Zanvyl Krieger School of Arts and Sciences (A.K.J.), Johns Hopkins University, Baltimore, MD; and Swedish Neuroscience Institute (J.W.H., D.S., L.M.C., M.J.D.), Seattle, WA.
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Citation
Holohemispheric developmental venous anomaly
Andrew K. Jung, John W. Henson, Daniel Susanto, Lisa M. Caylor, Michael J. Doherty
Neurology Apr 2013, 80 (18) 1718-1719; DOI: 10.1212/WNL.0b013e3182904fbb

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Developmental venous anomalies (DVA) are normally diminutive and incidental.1,2 In this 33-year-old patient with epilepsy, the DVA is holohemispheric. Her epilepsy probably originates from the left side based on semiology; the EEG displayed left-sided slowing. Axial T1-weighted sequences show skull atrophy, ventricular widening, and satellite cavernous malformations with accumulation of subacute blood products including hemosiderin (figure, A and B). T2 gradient echo illustrates pockets of chronic hemorrhage (figure, C and D). Engorged holohemispheric anomalous venous structures channel into ventricular periependymal veins, illustrated by mulitplanar T1 echo spin postcontrast sequences (figure, E and F). Time to minimum perfusion reflects elevated transit times, suggesting venous hypertension and capillary backpressures.

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Figure MRI of holohemispheric developmental venous anomaly

(A, B) Precontrast axial T1-weighted images. (C, D) Axial T2* gradient echo. (E, F) Postcontrast axial T1 spin echo. (G, H) Axial time to minimum perfusion map. (I) Postcontrast axial gradient echo T1 coronal.

Footnotes

  • Author contributions: A.K. Jung: drafting of manuscript, data collection. Dr. Henson: data collection, imaging review. Dr. Susanto: drafting of manuscript, imaging review. Dr. Caylor: drafting of manuscript, data collection. Dr. Doherty: manuscript coordination and drafting.

  • Study funding: No targeted funding reported.

  • Disclosure: The authors report no disclosures relevant to the manuscript. Go to Neurology.org for full disclosures.

  • © 2013 American Academy of Neurology

References

  1. 1.↵
    1. Aagaard BD,
    2. Song JK,
    3. Eskridge JM,
    4. Mayberg MR
    . Complex right hemisphere developmental venous anomaly associated with multiple facial hemangiomas. J Neurosurg 1999;90:766–769.
    OpenUrlCrossRefPubMed
  2. 2.↵
    1. Casey MA,
    2. Lahoti S,
    3. Gordhan A
    . Pediatric holohemispheric developmental venous anomaly: definitive characterization by 3D susceptibility weighted magnetic resonance angiography. J Radiol Case Rep 2011;5:10–18.
    OpenUrlPubMed

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