Liu Ying, Huo Liang, Zhang Jinhua, Liu Ying
Department of Pediatrics, The Fourth Affiliated Hospital of China Medical University, Shenyang, China.
Department of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, China.
Front Pediatr. 2021 Nov 3;9:716880. doi: 10.3389/fped.2021.716880. eCollection 2021.
Neuroblastoma (NB) is the most common pediatric extracranial solid neoplasm after leukemia. Intracranial metastases (IM) rarely occur in patients with NB. The present study aimed to review the clinical characteristics of NB patients from a single center presenting with IM. Two hundred children (aged 3-91 months) with NB admitted to the Fourth Affiliated Hospital of China Medical University between January 2009 and December 2015 were enrolled, and their clinical characteristics were recorded. The patients were divided into two groups based on the presence of IM. Their clinical characteristics, including demographics, clinical features, and laboratory and imaging studies, were retrospectively analyzed. IM occurred in 22 of 200 (11%) neuroblastoma patients, with a median age of 42.5 months (range, 3-91 months), with a male-to-female ratio of 1.4:1. Seven patients had IM at the initial diagnosis. Among the 15 children who did not have IM at initial presentation, the median interval from presentation to the diagnosis of IM was 17.3 months (range, 1-55 months). Compared with the control group, NB patients with IM tended to be asymptomatic at the time of NB diagnosis, which was made incidentally during routine physical examination (5 of 22, 22.7%, < 0.05). In addition, this group had more primary intra-abdominal sites (18 of 22, 81.8%, < 0.001) and worse prognosis (5 of 22, 22.7%, < 0.05). NB patients with IM have insidious onset in the early stage and a lower survival rate, especially patients with primary intra-abdominal lesions. Regular neurological monitoring could improve the rate of early diagnosis and prognosis of NB children with IM. Familiarity with the characteristic findings of NB with IM is necessary to avoid misdiagnosis and initiate necessary interventions.
神经母细胞瘤(NB)是白血病之后最常见的小儿颅外实体瘤。NB患者很少发生颅内转移(IM)。本研究旨在回顾单中心呈现IM的NB患者的临床特征。纳入2009年1月至2015年12月在中国医科大学附属第四医院收治的200例(年龄3 - 91个月)NB患儿,并记录其临床特征。根据是否存在IM将患者分为两组。对其临床特征,包括人口统计学、临床特征以及实验室和影像学检查结果进行回顾性分析。200例神经母细胞瘤患者中有22例(11%)发生IM,中位年龄为42.5个月(范围3 - 91个月),男女比例为1.4:1。7例患者在初次诊断时即有IM。在初次就诊时无IM的15例患儿中,从就诊到诊断为IM的中位间隔时间为17.3个月(范围1 - 55个月)。与对照组相比,发生IM的NB患者在NB诊断时往往无症状,多在常规体检时偶然发现(22例中的5例,22.7%,<0.05)。此外,该组更多为原发性腹内病灶(22例中的18例,81.8%,<0.001)且预后较差(22例中的5例,22.7%,<0.05)。发生IM的NB患者早期发病隐匿且生存率较低,尤其是原发性腹内病变患者。定期进行神经学监测可提高IM的NB患儿的早期诊断率和预后。熟悉NB合并IM的特征性表现对于避免误诊和启动必要干预措施很有必要。