Stroke in sickle cell disease in association with bilateral absence of the internal carotid arteries. Case report

Ivana Markovic, Zoran Milenkovic*, Bosanka Jocic-Jakubi, Amna Al Futaisi, Kakaria Anupam Kakaria, Yasser Walli

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Congenital absence of the internal carotid artery (ICA) is a highly infrequent congenital incidence and occurs in less than 0.01% of the population; bilateral absence is exceedingly rare, diagnosed below 10% of the unilateral absence of the ICA. Sickle cell disease (SCD) is a serious disorder and carries a high risk of stroke. Case presentation: We present a five-year-old child with SCD who experienced an ischemic stroke episode with epileptic seizures. Neuroimaging revealed the agenesis of both ICAs. The frequency, embryology, and collateral pathway of the vascular anomaly as the clinical presentation, of this rare hematologic disease, are discussed. Conclusions: Sickle cell disease (SCD) carries a high risk of stroke. Congenital absence of ICA occurs in less than 0.01% of the population; bilateral absence is diagnosed below 10% of the unilateral absence of the ICA.

Original languageEnglish
Article number182
JournalBMC Neurology
Volume22
Issue number1
DOIs
Publication statusPublished - Dec 2022

Keywords

  • Agenesis
  • Internal carotid artery
  • Seizure
  • Sickle cell disease
  • Stroke

ASJC Scopus subject areas

  • Clinical Neurology

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