Wang Lin, Duan Hongyu, Zhou Kaiyu, Hua Yimin, Liu Xiaoliang, Wang Chuan
Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education Chengdu, Sichuan University, Chengdu, China.
Department of Pediatric Cardiology, West China Second University Hospital, Sichuan University, Chengdu, China.
Front Pediatr. 2021 May 19;9:598867. doi: 10.3389/fped.2021.598867. eCollection 2021.
Cerebral infarction is a rare neurological complication of Kawasaki disease (KD) and occurs in the acute or subacute stage. There have been no reported cases of late-onset fatal cerebral infarction presenting over 1 year after the onset of KD. A 5-month-old male patient with KD received timely intravenous immunoglobulin therapy; however, extensive coronary artery aneurysms (CAA) and coronary artery thrombosis (CAT) developed 1 month later. Anticoagulation and thrombolytic agents were suggested, but the child's parents refused. Fifteen months after KD onset, an attack of syncope left him with left hemiplegia; brain computerized tomography (CT) scans revealed cerebral infarction of the right basal ganglion without hemorrhage. Magnetic resonance angiography (MRA) revealed severe stenosis of the right middle cerebral artery, and a series of tests were performed to exclude other causes of cerebral infarction. Considering the cerebral infarction and CAT, combination therapy with urokinase and low-molecular-weight heparin (LMWH) was initiated within 24 h of syncope onset, together with oral aspirin and clopidogrel. Five days later, his clinical symptoms partially regressed and he was discharged. Unfortunately, 5 days after discharge, his clinical condition suddenly deteriorated. Repeat brain CT showed hemorrhagic stroke involving the entire left cerebral area, in addition to the previous cerebral infarction in the right basal ganglion, with obvious secondary cerebral swelling and edema, which might have been caused by previous thrombolysis. Severe cerebral hernias developed quickly. Regrettably, the patient's parents abandoned treatment because of economic factors and unfavorable prognosis, and he died soon after. Cerebral infarction and cerebral artery stenosis can develop late, even 1 year after the onset of KD. Pediatricians should be aware of the possibility of cerebrovascular involvement in addition to cardiac complications during long-term follow-up of KD patients. Prompt anticoagulation therapy and regular neuroimaging evaluation are essential for the management of patients with KD with giant CAA and/or CAT.
脑梗死是川崎病(KD)罕见的神经系统并发症,发生于急性期或亚急性期。尚无KD发病1年以上出现迟发性致命性脑梗死的病例报道。一名5个月大的KD男性患者接受了及时的静脉注射免疫球蛋白治疗;然而,1个月后出现了广泛的冠状动脉瘤(CAA)和冠状动脉血栓形成(CAT)。建议使用抗凝和溶栓药物,但患儿家长拒绝了。KD发病15个月后,一次晕厥发作导致他出现左侧偏瘫;脑部计算机断层扫描(CT)显示右侧基底节脑梗死,无出血。磁共振血管造影(MRA)显示右侧大脑中动脉严重狭窄,并进行了一系列检查以排除脑梗死的其他病因。考虑到脑梗死和CAT,在晕厥发作后24小时内开始联合使用尿激酶和低分子肝素(LMWH)治疗,同时口服阿司匹林和氯吡格雷。5天后,他的临床症状部分缓解并出院。不幸的是,出院5天后,他的病情突然恶化。重复脑部CT显示,除了之前右侧基底节的脑梗死外,整个左侧脑区出现出血性中风,伴有明显的继发性脑肿胀和水肿,这可能是由之前的溶栓治疗引起的。严重的脑疝迅速发展。遗憾的是,由于经济因素和预后不佳,患者家长放弃了治疗,他不久后死亡。脑梗死和脑动脉狭窄可在KD发病后较晚出现,甚至在发病1年后。儿科医生在对KD患者进行长期随访时,除了心脏并发症外,应意识到脑血管受累的可能性。及时的抗凝治疗和定期的神经影像学评估对于患有巨大CAA和/或CAT的KD患者的管理至关重要。