Callosal warning syndrome

Ramachandiran Nandhagopal*, Abdullah Al-Asmi, William James Johnston, P. C. Jacob, G. R. Arunodaya

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Citations (Scopus)

Abstract

Objective: To report the clinical and imaging findings in a patient with an initial fluctuating disconnection syndrome due to corpus callosal ischemia that ultimately culminated in infarction with persistent symptoms. Case report: A 40-year-old, hypertensive, right-handed man presented with transient, stereotyped symptoms of corpus callosal disconnection (intermanual conflict, apraxia, dysgraphia and construction difficulties in his left hand). Serial magnetic resonance imaging scans demonstrated the ischemic nature of the initial fluctuating symptoms and later showed callosal infarction when the symptoms were persistent. Magnetic resonance angiogram did not reveal significant stenosis or occlusion of the internal carotid or proximal portion of anterior cerebral arteries. Patient received standard treatment for ischemic stroke and at follow-up 1 month later, had mild left hand apraxia, dysgraphia and construction difficulties. Conclusion: The case highlights the unusual occurrence of crescendo transient ischemic attacks culminating in infarction in the location of corpus callosum. We have termed this novel stroke syndrome as 'callosal warning syndrome' as the temporal profile was quite indistinguishable from that of relatively well-known stroke warning syndromes in the location of internal capsule and pontine tegmentum.

Original languageEnglish
Pages (from-to)178-180
Number of pages3
JournalJournal of the Neurological Sciences
Volume314
Issue number1-2
DOIs
Publication statusPublished - Mar 15 2012
Externally publishedYes

Keywords

  • Callosal infarction
  • Disconnection syndrome
  • Stroke warning syndrome

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

Fingerprint

Dive into the research topics of 'Callosal warning syndrome'. Together they form a unique fingerprint.

Cite this