Slator Naomi, Talibi Sayed Samed, Mundil Nilesh, Thomas Allan, Lamin Saleh, Walsh Richard, Rodrigues Desiderio, Solanki Guirish A
Department of Paediatric Neurosurgery, Birmingham Children's Hospital, Birmingham, UK.
Department of Neurosurgery, Queen Elizabeth Hospital, Birmingham, UK.
Childs Nerv Syst. 2019 Jul;35(7):1197-1205. doi: 10.1007/s00381-019-04159-3. Epub 2019 May 14.
Paediatric intracranial aneurysms are rare, with a differing natural history and thought to account for only up to 7% of all intracranial aneurysms. There is much uncertainty that surrounds the prevalence of unruptured intracranial aneurysms and it is estimated to be anywhere between 2 and 90 per 1000. This is the largest British single-centre analysis of paediatric intracranial aneurysms. We present the patient course from their initial presentations to the outcome of treatment and evaluate a serial assessment of adequacy of aneurysmal obliteration radiologically.
Twenty-two paediatric cases were identified that required treatment. The median age of presentation was 11.3 years (mean 9.9, range 0 to 15.9), 68% (15/22) were male and 77% (17/22) were ruptured on presentation. The majority of aneurysms were located at the anterior circulation (77% (17/22)). The overall median aneurysm size (n = 21) was 7.4 mm (mean 5 mm, range 2.5-19 mm). Twenty patients survived the acute phase and 80% (16/20) underwent coil embolisation and the other patients' surgical clipping. The overall outcomes were available for the 20 patients; on discharge, 90% (18/20) had a favourable clinical outcome (GOS score of 3-5). Treatment-specific clinical favourable outcomes were 88% (14/16) for coil embolisation against 100% (4/4) after surgical clipping. Of the two patients that died in the acute phase, one had sickle cell anaemia. Aneurysm aetiology was unknown in all other cases. None of the patients had a family history of aneurysms.
Paediatric intracranial aneurysms while rare should be considered a differential diagnosis of children presenting with unexplained loss of consciousness with or without focal neurological deficit and/or headache. There is a two to one preponderance for males with a larger proportion of aneurysms within the posterior circulation (25%). Coil embolisation is the preferred method of securing a paediatric intracranial aneurysm.
小儿颅内动脉瘤较为罕见,其自然病史各异,据认为仅占所有颅内动脉瘤的7%。未破裂颅内动脉瘤的患病率存在诸多不确定性,估计每1000人中有2至90例。这是英国最大规模的小儿颅内动脉瘤单中心分析。我们展示了患者从最初就诊到治疗结果的病程,并通过影像学对动脉瘤闭塞的充分性进行了系列评估。
共确定22例需要治疗的小儿病例。就诊时的中位年龄为11.3岁(平均9.9岁,范围0至15.9岁),68%(15/22)为男性,77%(17/22)就诊时已破裂。大多数动脉瘤位于前循环(77%(17/22))。动脉瘤的总体中位大小(n = 21)为7.4毫米(平均为5毫米,范围2.5至19毫米)。20例患者度过急性期存活,其中80%(16/20)接受了弹簧圈栓塞,其他患者接受了手术夹闭。20例患者的总体结果可得;出院时,90%(18/20)临床结果良好(格拉斯哥预后评分3至5分)。弹簧圈栓塞的治疗特异性临床良好结果为88%(14/16),手术夹闭后为100%(4/4)。在急性期死亡的2例患者中,1例患有镰状细胞贫血。所有其他病例的动脉瘤病因均不明。所有患者均无动脉瘤家族史。
小儿颅内动脉瘤虽罕见,但对于出现不明原因意识丧失且伴有或不伴有局灶性神经功能缺损和/或头痛的儿童应考虑作为鉴别诊断。男性与女性比例为二比一,后循环中的动脉瘤比例较大(25%)。弹簧圈栓塞是治疗小儿颅内动脉瘤的首选方法。