Proust F, Toussaint P, Garniéri J, Hannequin D, Legars D, Houtteville J P, Fréger P
Department of Neurosurgery, Rouen University Hospital, France.
J Neurosurg. 2001 May;94(5):733-9. doi: 10.3171/jns.2001.94.5.0733.
The exceptional pediatric aneurysm can be distinguished from its adult counterpart by its location and size; however, patient outcomes remain difficult to evaluate based on the published literature.
Twenty-two children, all consecutively treated in three neurosurgery departments, were included in this study. Each patient's preoperative status was determined according to the Hunt and Hess classification. Routine computerized tomography scanning and angiography were performed in all children on the 10th postoperative day. Each patient's clinical status was evaluated 2 to 10 years postoperatively by applying the Glasgow Outcome Scale (GOS). Twenty-one children presented with a subarachnoid hemorrhage (SAH) and one child harbored an asymptomatic giant aneurysm. Thirteen patients were in good preoperative grade (Hunt and Hess Grades I to III) and eight in poor preoperative grade (Hunt and Hess Grade IV or V). The symptomatic aneurysms were located on the internal carotid artery bifurcation (36.4%); middle cerebral artery (36.4%), half of which were found on the distal portion; anterior communicating artery (18.2%); and within the vertebrobasilar system (9.1%). A giant aneurysm was observed in 14% of patients. Overall outcome was favorable (GOS Score 5) in 14 children (63.6%) and death occurred in five (22.7%). Causes of unfavorable outcome included the initial SAH in four children, a complication in procedure in three children, and edema in one child.
Pediatric aneurysms have a specific distribution unlike that of aneurysms in the adult population. The incidence of giant aneurysms and outcomes were similar to those in the adult population. The major cause of poor outcome was the initial SAH, in particular, the high proportion of rebleeding possibly due to a delay in diagnosis.
特殊的小儿动脉瘤可通过其位置和大小与成人动脉瘤相区分;然而,根据已发表的文献,患者的预后仍然难以评估。
本研究纳入了在三个神经外科连续接受治疗的22名儿童。根据Hunt和Hess分级确定每位患者的术前状态。所有儿童在术后第10天进行常规计算机断层扫描和血管造影。术后2至10年,采用格拉斯哥预后量表(GOS)评估每位患者的临床状态。21名儿童出现蛛网膜下腔出血(SAH),1名儿童患有无症状巨大动脉瘤。13例患者术前分级良好(Hunt和Hess分级I至III级),8例患者术前分级较差(Hunt和Hess分级IV或V级)。有症状的动脉瘤位于颈内动脉分叉处(36.4%);大脑中动脉(36.4%),其中一半位于远端;前交通动脉(18.2%);以及椎基底动脉系统内(9.1%)。14%的患者观察到巨大动脉瘤。14名儿童(63.6%)的总体预后良好(GOS评分5分),5名儿童(22.7%)死亡。不良预后的原因包括4名儿童最初的SAH、3名儿童手术并发症和1名儿童水肿。
小儿动脉瘤具有与成人动脉瘤不同的特定分布。巨大动脉瘤的发生率和预后与成人相似。不良预后的主要原因是最初的SAH,特别是可能由于诊断延迟导致的再出血比例较高。