DU Y Y, Wang J, He L, Ji L N, Xu X W
Department of Pediatrics, Beijing Tsinghua Changgung Hospital Affiliated to Tsinghua University, School of Clinical Medicine of Tsinghua University, Beijing 102218, China.
Department of Gastroenterology, Beijing Children' s Hospital affiliated to Capital Medical University & National Center for Children' s Health, Beijing 100045, China.
Beijing Da Xue Xue Bao Yi Xue Ban. 2022 Aug 18;54(4):756-761. doi: 10.19723/j.issn.1671-167X.2022.04.028.
We reported a pediatric case of Kawasaki disease complicated with mild encephalitis/encephalopathy with a reversible splenial lesion (MERS) from Beijing Tsinghua Changgung Hospital. The clinical data were retrospectively analyzed and the related literature was reviewed. The clinical features, treatment and prognosis of the disease were summarized to improve recognition of Kawasaki disease complicated with MERS. A 7-year-old boy was diagnosed with Kawasaki disease due to continuous high fever for 6 d, accompanied by strawberry tongue, conjunctival congestion, erythema-like hyperemia rash, and cervical enlarged lymph nodes. And treatment was started with intravenous immunoglobulin (IVIG: 2 g/kg) and oral aspirin [40 mg/(kg·d)]. Twenty-four hours after the treatment of IVIG, the patient' s fever persisted and in addition he developed headache and drowsiness. His cranial magnetic resonance imaging (MRI) demonstrated a localized lesion in the splenium of the corpus callosum with high intensity signal on diffusion-weighted images (DWI) and T2-weighted, and low intensity signal on apparent diffusion coefficient (ADC) and T1-weighted. Based on these findings, he was diagnosed with MERS-complicated Kawasaki disease. Methylprednisolone [2 mg/(kg·d)] treatment was started intravenously, and within several hours he was afebrile and the neurological symptoms disappeared. A follow-up MRI was conducted after 1 week was normal. He was discharged without any neurological sequelae and coronary artery lesions. A total of 12 qualified foreign literature were retrieved, with no Chinese literature searched. Seventeen children were reported, the median age was 6.5 years (range: 1-14 years), among them 11 cases were children over 5 years old, and 4 cases were complicated with coronary artery lesions. All children had neurological symptoms, such as consciousness disorder, visual hallucination or convulsion. MRI conformed to MERS imaging changes. After active treatment, the neurological manifestations and radiological abnormalities completely disappeared, leaving no neurological sequelae. Kawasaki disease complicated with MERS had not been reported in China by now. Literature that identified Kawasaki disease complicated with MERS mostly occurred in children over 5 years old. Cranial MRI examination is helpful for early diagnosis. Timely treatment can reverse MERS in a short time, without neurological sequelae left.
我们报道了北京清华长庚医院1例川崎病合并轻度脑炎/脑病伴可逆性胼胝体压部病变(MERS)的儿科病例。对临床资料进行回顾性分析并复习相关文献。总结该疾病的临床特征、治疗及预后情况,以提高对川崎病合并MERS的认识。一名7岁男孩因持续高热6天,伴有草莓舌、结膜充血、红斑样充血性皮疹及颈部淋巴结肿大而被诊断为川崎病。开始静脉注射免疫球蛋白(IVIG:2 g/kg)及口服阿司匹林[40 mg/(kg·d)]进行治疗。IVIG治疗24小时后,患儿仍发热,此外还出现头痛及嗜睡症状。其头颅磁共振成像(MRI)显示胼胝体压部有局限性病变,在扩散加权成像(DWI)及T2加权像上呈高信号,在表观扩散系数(ADC)及T1加权像上呈低信号。基于这些表现,他被诊断为川崎病合并MERS。开始静脉注射甲泼尼龙[2 mg/(kg·d)]治疗,数小时内患儿体温恢复正常,神经症状消失。1周后复查MRI正常。患儿出院时无任何神经后遗症及冠状动脉病变。共检索到12篇合格的外文文献,未检索到中文文献。报道了17例患儿,中位年龄为6.5岁(范围:1 - 14岁),其中11例为5岁以上儿童,4例合并冠状动脉病变。所有患儿均有神经症状,如意识障碍、视幻觉或惊厥。MRI符合MERS影像学改变。积极治疗后,神经表现及影像学异常完全消失,无神经后遗症。目前国内尚未报道川崎病合并MERS的病例。已发现川崎病合并MERS多见于5岁以上儿童。头颅MRI检查有助于早期诊断。及时治疗可在短时间内使MERS逆转,不留神经后遗症。