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

被引:2
作者
Markovic, Ivana [1 ]
Milenkovic, Zoran [2 ]
Jocic-Jakubi, Bosanka [3 ]
Al Futaisi, Amna [4 ]
Kakaria, Kakaria Anupam [5 ]
Walli, Yasser [3 ]
机构
[1] Sultan Qaboos Univ Hosp, Radiol Dept, IvanaMarkov, Muscat, Oman
[2] Gen Hosp Sava Surg, Kej 29 Decembar 2, Nish 18000, Serbia
[3] Sultan Qaboos Univ Hosp, Dept Child Hlth, Muscat, Oman
[4] Sultan Qaboos Univ Hosp, Hosp, Coll Med & Hlth Sci, Child Hlth, Muscat, Oman
[5] Sultan Qaboos Univ Hosp, Dept Radiol & Mol Imaging, Muscat, Oman
关键词
Sickle cell disease; Stroke; Seizure; Internal carotid artery; Agenesis; SILENT CEREBRAL INFARCTS; CONGENITAL ABSENCE; ISCHEMIC-STROKE; CHILDREN; AGENESIS; MANAGEMENT; SEIZURES;
D O I
10.1186/s12883-022-02702-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 KAs. 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.
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