Li Da, Hao Shu-Yu, Tang Jie, Xiao Xin-Ru, Jia Gui-Jun, Wu Zhen, Zhang Li-Wei, Zhang Jun-Ting
Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, People's Republic of China.
J Neurosurg Pediatr. 2014 May;13(5):471-83. doi: 10.3171/2014.2.PEDS13487. Epub 2014 Mar 17.
The aim of this study was to investigate the clinical appearance of untreated pediatric brainstem cavernous malformations (CMs) and to identify the hemorrhage risks and functional outcomes.
All pediatric patients with a diagnosis of brainstem CM between 1985 and 2012 were registered. The clinical chart and radiographs were recorded, and follow-up evaluations were obtained prospectively.
A total of 85 patients (69.4% male) were included with a mean age of 12.7 years. Sixty-seven patients (78.8%) had prior hemorrhage, and 6 patients (7.1%) were asymptomatic. There were 15 midbrain lesions, 53 pons lesions, and 17 medulla lesions. The mean lesion size was 1.9 cm. During a total of 401.6 patient-years of follow-up, 47 hemorrhages occurred in 37 patients, and the annual hemorrhage rate was 11.7% per patient-year. The mean hemorrhage interval was 47.8 months. The hemorrhage risk declined over time, especially after the first 2 years. Both a lesion size ≥ 2 cm (hazard ratio [HR] 2.122, p = 0.037) and the presence of perilesional edema (HR 2.192, p = 0.039) predicted future hemorrhage and were associated with a high annual hemorrhage rate. The hemorrhage-free survival at 6 months was 85.7%, and at 1, 5, 10, and 15 years was 71.5%, 49.4%, 27.5%, and 13.7%, respectively. At the most recent functional evaluation, 33 patients (38.8%) had improved, 32 (37.6%) had stabilized, and 20 (23.5%) had worsened, without any deaths. Twenty-two patients (25.9%) obtained a full recovery. Prospective hemorrhage (HR 0.191, p = 0.003) was the adverse predictor for full recovery. Full recovery primarily occurred within the first 12 months, after which the chance of full recovery decreased. The cumulative percentage of complete recovery at 6 months was 32.7%, and at 1, 3, and 5 years was 40.8%, 43.6%, and 49.2%, respectively.
In this study the hemorrhage rate was relatively high in pediatric brainstem CMs, although the functional outcome was acceptable. The decline in hemorrhage risk and the identified adverse predictors in this study were helpful for clinicians and patients when deciding on treatment. Referral bias and the insufficient follow-up period of the study were highlighted as limitations.
本研究旨在调查未经治疗的小儿脑干海绵状血管畸形(CMs)的临床表现,确定出血风险和功能转归。
登记1985年至2012年间所有诊断为脑干CM的小儿患者。记录临床病历和影像学资料,并进行前瞻性随访评估。
共纳入85例患者(男性占69.4%),平均年龄12.7岁。67例患者(78.8%)曾有过出血,6例患者(7.1%)无症状。有15例中脑病变、53例脑桥病变和17例延髓病变。病变平均大小为1.9 cm。在总共401.6患者年的随访期间,37例患者发生了47次出血,年出血率为每位患者年11.7%。平均出血间隔为47.8个月。出血风险随时间下降,尤其是在最初2年后。病变大小≥2 cm(风险比[HR]2.122,p = 0.037)和病灶周围水肿的存在(HR 2.192,p = 0.039)均预示未来会出血,并与高年出血率相关。6个月时无出血生存率为85.7%,1年、5年、10年和15年时分别为71.5%、49.4%、27.5%和13.7%。在最近一次功能评估中,33例患者(38.8%)病情改善,32例(37.6%)病情稳定,20例(23.5%)病情恶化,无死亡病例。22例患者(25.9%)完全康复。前瞻性出血(HR 0.191,p = (此处原文可能有误,推测为0.003))是完全康复的不良预测因素。完全康复主要发生在最初12个月内,此后完全康复的机会降低。6个月时完全康复的累积百分比为32.7%,1年、3年和5年时分别为40.8%、43.6%和49.2%。
在本研究中,小儿脑干CM的出血率相对较高,尽管功能转归尚可接受。本研究中出血风险的下降以及确定的不良预测因素有助于临床医生和患者在决定治疗时参考。研究存在转诊偏倚和随访期不足的局限性。