Parenrengi Muhammad Arifin, Suryaningtyas Wihasto, Fauza Joandre
Department of Neurosurgery, Faculty of Medicine, Universitas Airlangga, Dr Soetomo Academic General Hospital, Indonesia.
Int J Surg Case Rep. 2021 Sep;86:106347. doi: 10.1016/j.ijscr.2021.106347. Epub 2021 Aug 31.
Ruptured arteriovenous malformations (AVM) hold a larger proportion as the cause of spontaneous intracranial hemorrhage in children compared to those in adults. Although surgical excision still remains as the gold standard therapy for arteriovenous malformations, some smaller ones are reported to resolve from embolization alone. However, difficulty arises when small arteriovenous malformations are not detected on certain diagnostic modalities such as Computed Tomography Angiography (CTA), giving rise to false negatives, which may compromise appropriate management of patients. Endovascular embolization can be used as alternative options as diagnostic and therapy for invisible arteriovenous malformation in children. We report two cases of ruptured paediatrics arteriovenous malformations with a complication of hydrocephalus, managed with endovascular embolization and a cerebrospinal fluid diversionary procedure.
We report 2 case in from Dr. Soetomo academic general hospital in 2021, the first case was a fully conscious 6-year-old-female child with sudden left-sided weakness and severe headache in January, and the second case a 9-year-old female came with decreased consciousness in May. Both had evidence of intracerebral hemorrhage, intraventricular hemorrhage, and hydrocephalus on head radiological examination, but no visible vascular malformations on Computed Tomography Angiography. The first patient was treated with extra ventricular drainage initially, while the second case was not. Transfemoral cerebral angiography revealed small arteriovenous malformations in both patients, and both had successful endovascular embolization afterwards. The first case was shunt-free, while the second case had her drainage switched to ventriculoperitoneal shunt right after the embolization procedure. Both patients recovered fully without complications and sequelae, and were discharged afterwards.
Both patients did not undergo surgical resection of the arteriovenous malformations; the first case only underwent endovascular embolization, while the second case underwent embolization and ventriculoperitoneal shunting. The cases described here help highlight the irreplaceable role of Transfemoral Cerebral Angiography as a gold standard for cases for arteriovenous malformations compared to other modalities, such as Computed Tomography Angiography (CTA). Smaller arteriovenous malformations in paediatrics are reported to achieve complete radiological resolution, and cerebrospinal fluid diversion in hydrocephalic cases are not always performed. Several factors to be considered include initial consciousness and severity of neurological deficit, which were taken into account in the management of our patients.
Embolization procedures may be beneficial in some pediatric arteriovenous malformations, preferably in smaller ones that undetectable by angiography. Several factors such as the consciousness and neurological deficit upon initial presentation may help in the decision making of these cases.
与成人相比,破裂的动静脉畸形(AVM)在儿童自发性颅内出血原因中占比更大。尽管手术切除仍是动静脉畸形的金标准治疗方法,但据报道一些较小的动静脉畸形仅通过栓塞就能治愈。然而,当在某些诊断方式(如计算机断层血管造影术(CTA))上未检测到小型动静脉畸形时,就会出现困难,从而产生假阴性结果,这可能会影响对患者的适当管理。血管内栓塞可作为儿童隐匿性动静脉畸形的诊断和治疗的替代选择。我们报告两例破裂的儿科动静脉畸形并伴有脑积水并发症的病例,采用血管内栓塞和脑脊液分流术进行治疗。
我们报告了2021年来自苏托莫博士学术综合医院的2例病例,第一例是一名1月份突然出现左侧肢体无力和严重头痛的6岁神志清醒女童,第二例是一名5月份出现意识减退的9岁女童。两人头部影像学检查均有脑出血、脑室内出血和脑积水的证据,但计算机断层血管造影未发现明显的血管畸形。第一例患者最初接受了脑室外引流治疗,而第二例患者未接受该治疗。经股动脉脑血管造影显示两名患者均有小型动静脉畸形,随后两人均成功进行了血管内栓塞。第一例患者无需分流,而第二例患者在栓塞术后将引流改为脑室腹腔分流。两名患者均完全康复,无并发症和后遗症,随后出院。
两名患者均未接受动静脉畸形的手术切除;第一例仅接受了血管内栓塞,而第二例接受了栓塞和脑室腹腔分流术。此处描述的病例有助于突出经股动脉脑血管造影术相对于其他方式(如计算机断层血管造影术(CTA))作为动静脉畸形病例金标准的不可替代作用。据报道,儿科较小的动静脉畸形可实现完全的影像学消退,脑积水病例并不总是进行脑脊液分流。需要考虑的几个因素包括初始意识和神经功能缺损的严重程度,我们在患者管理中已将这些因素考虑在内。
栓塞程序可能对某些儿科动静脉畸形有益,最好是对血管造影无法检测到的较小动静脉畸形。初始表现时的意识和神经功能缺损等几个因素可能有助于这些病例的决策。