Vafaeeshahi Mohammad, Azizishalbaf Nazanin, Tahernia Leila
Pediatric Neurology, Pediatric Growth and Development Research center, Institute of Endocrinology and Metabolism, Iran University of Medical Sciences, Tehran, Iran.
Pediatric Emergency, Zanjan University of Medical Sciences, Zanjan, Iran.
Iran J Child Neurol. 2019 Winter;13(1):107-114.
Cerebellar acute ischemic stroke (AIS) can be a complication of minor head trauma, vertebral artery dissection, vasospasm or systemic hypoperfusion. CT scan usually is negative few hours after acute infarction. Magnetic resonance imaging (MRI) is superior to CT scan for posterior fossa lesions and also in acute phase of cerebellar stroke especially in children. Here we report a 9 yr old girl referred to the Pediatric Emergency Room, Moosavi Hospital, Zanjan, Iran in January 2017 presenting with sudden onset of headache and recurrent vomiting, ataxia, and history of 3 consecutive days of fever and malaise. In the report of MRI, there were abnormal low T1 and high T2 signal intensity in left cerebellar hemisphere involving superior and middle cerebellar peduncles. After 4 days of admission, the patient became drowsy, symptoms progressed and transferred to the pediatric intensive care unit (PICU). The patient underwent hemispherectomy surgery of the left cerebellar hemisphere because of acute obstructive hydrocephaly. After 5 months of occupational therapy, the force of her extremities was normal and the ataxia completely disappeared. Childhood acute ischemic stroke although rare can happen with cerebellar involvement. Because in our patient the first brain CT scan was nearly normal and a false negative rate for initial computed tomography (CT) scanning of 60%-80% also contributes to missed and delayed diagnosis of childhood AIS, for every child presenting with acute ataxia without identified cause in addition to CT scan, MRI also being ordered and from the beginning besides other causes, stroke be contemplated as a cause of ataxia.
小脑急性缺血性卒中(AIS)可能是轻微头部外伤、椎动脉夹层、血管痉挛或全身性低灌注的并发症。急性梗死数小时后,CT扫描通常呈阴性。对于后颅窝病变,磁共振成像(MRI)优于CT扫描,在小脑卒中急性期尤其是儿童中也是如此。在此,我们报告一名9岁女孩,于2017年1月转诊至伊朗赞詹穆萨维医院儿科急诊室,表现为突发头痛、反复呕吐、共济失调,并有连续3天发热和不适的病史。MRI报告显示,左小脑半球包括小脑上脚和小脑中脚有异常低T1和高T2信号强度。入院4天后,患者变得嗜睡,症状进展并转入儿科重症监护病房(PICU)。由于急性梗阻性脑积水,患者接受了左小脑半球切除术。经过5个月的职业治疗,她四肢的力量恢复正常,共济失调完全消失。儿童急性缺血性卒中虽然罕见,但可累及小脑。因为在我们的患者中,首次脑部CT扫描几乎正常,初始计算机断层扫描(CT)的假阴性率为60%-80%,这也导致了儿童AIS的漏诊和延迟诊断,所以对于每一名出现急性共济失调且病因不明的儿童,除了CT扫描外,还应进行MRI检查,并且从一开始除了考虑其他病因外,还应将卒中视为共济失调的一个病因。