Gowda Vykuntaraju K, Manjeri Vidya, Srinivasan Varunvenkat M, Sajjan Sushma V, Benakappa Asha
Department of Pediatric Neurology, Indira Gandhi Institute of Child Health, Bengaluru, Karnataka, India.
Department of Pediatrics, Indira Gandhi Institute of Child Health, Bengaluru, Karnataka, India.
J Pediatr Neurosci. 2018 Oct-Dec;13(4):448-454. doi: 10.4103/JPN.JPN_89_17.
Basal ganglia stroke following trauma has been known to occur and described in previous case studies. But exact etiology is unknown.
To study the clinical characteristics, imaging features, and neurodevelopmental outcomes of children presented with basal ganglia stroke associated with mineralization in the lenticulostriate arteries in our center from January 2013 to June 2016.
Children with subcortical stroke during the study period were identified retrospectively, and those presented with basal ganglia stroke with mineralization of lenticulostriate vessels were analyzed for clinical profile, imaging features, and outcomes. Statistical analysis was carried out using the Statistical Package for the Social Sciences (SPSS) software, version 17 (IBM, New York).
Of 38 children with basal ganglia stroke (20 boys, 18 girls, and mean age at presentation 14.026±5.8470 months), 27 had history of trauma preceding the stroke. Thirty-seven children presented with hemiparesis and one presented with hemidystonia. The mean follow-up time was 8 months, three children developed recurrence during that period. Five children with recurrence of stroke, initial episodes were not evaluated as they presented to us for the first time. A total of 17 of 30 infants who did not have stroke recurrence were normal on follow-up, whereas 9 infants showed persistent mild hemiparesis, 2 had motor delay, and 2 others had mild residual distal weakness. No identifiable causes were observed for vascular calcification. Two familial cases were also noted.
Most common cause for acute basal ganglia stroke in toddlers was mineralizing angiopathy of lenticulostriate vessels. It was preceded by minor trauma in most cases.
创伤后基底节区卒中已在既往病例研究中被发现并描述。但其确切病因尚不清楚。
研究2013年1月至2016年6月在我院出现基底节区卒中并伴有豆纹动脉矿化的儿童的临床特征、影像学特征及神经发育结局。
回顾性确定研究期间患有皮质下卒中的儿童,并对那些出现基底节区卒中且豆纹血管矿化的儿童进行临床特征、影像学特征及结局分析。使用社会科学统计软件包(SPSS)17版(IBM,纽约)进行统计分析。
38例基底节区卒中患儿(20例男孩,18例女孩,发病时平均年龄14.026±5.8470个月)中,27例在卒中前有创伤史。37例患儿出现偏瘫,1例出现偏侧肌张力障碍。平均随访时间为8个月,在此期间3例患儿复发。5例卒中复发患儿,因首次就诊时未对初始发作进行评估。30例未出现卒中复发的婴儿中,共有