Prasad G Lakshmi, Gupta Deepak Kumar, Sharma Bhawani Shankar, Mahapatra Ashok Kumar
Pediatr Neurosurg. 2015;50(5):250-6. doi: 10.1159/000438488. Epub 2015 Aug 20.
Traumatic posterior fossa extradural hematomas (PFEDH) are rare lesions constituting <10% of all extradural hematomas. Reliance on clinical findings alone is not recommended as these are nonspecific; for all suspicious cases, it is advisable to conduct a CT scan. Only a handful of pediatric studies have been reported analyzing the outcome of such lesions. The aim of our study was to analyze outcomes for children with PFEDH managed at our apex trauma center.
We conducted a retrospective analysis of pediatric patients (≤18 years) admitted with a diagnosis of traumatic PFEDH from January 2008 to February 2014.
Of 22 patients, 16 were managed surgically (group 1) and 6 conservatively (group 2); 1 failed conservative treatment (due to an increased EDH volume). Mean age was 11.7 years (range 2-18 years). Falls were the most common cause of injury. Vomiting and loss of consciousness were the most frequent presenting features. There were 18 mild, 2 moderate and 2 severe head injuries. The mean volume of EDH was 37.1 ml (range 18-100 ml) and 10.3 ml (8-16 ml) in the operative and conservative subgroups, respectively. Occipital bone fracture was seen in 16 cases with supratentorial extension in 11. Four complications were noted in 3 cases. Mean follow-up duration was 25.1 months (range 3-34 months). Except for 1 patient, all had excellent outcomes. There was no mortality.
Traumatic pediatric PFEDHs are rare. Both the clinical status of the patient and the volume of the hematoma need to be assessed before deciding on surgery. Most cases have associated occipital bone fractures and around half have supratentorial extension; these need to be carefully assessed preoperatively. Torrential venous bleeding can be a major problem due to rupture of the adjacent sinuses. Timely intervention is crucial for achieving good outcome, keeping in view a low threshold for surgical evacuation. Although not innovative, this second-largest case series provides additional data and contributes to the existing literature on such lesions in pediatric patients.
创伤性后颅窝硬膜外血肿(PFEDH)是罕见病变,占所有硬膜外血肿的比例不到10%。不建议仅依靠临床症状来诊断,因为这些症状缺乏特异性;对于所有可疑病例,建议进行CT扫描。仅有少数儿科研究报道了此类病变的治疗结果分析。本研究的目的是分析在我们顶级创伤中心接受治疗的儿童PFEDH的治疗结果。
我们对2008年1月至2014年2月期间因创伤性PFEDH入院的儿科患者(≤18岁)进行了回顾性分析。
22例患者中,16例接受手术治疗(第1组),6例接受保守治疗(第2组);1例保守治疗失败(因硬膜外血肿体积增大)。平均年龄为11.7岁(范围2 - 18岁)。跌倒为最常见的受伤原因。呕吐和意识丧失是最常见的症状。有18例轻度、2例中度和2例重度颅脑损伤。手术组和保守组硬膜外血肿的平均体积分别为37.1 ml(范围18 - 100 ml)和10.3 ml(8 - 16 ml)。16例可见枕骨骨折,其中11例伴有幕上扩展。3例出现4种并发症。平均随访时间为25.1个月(范围3 - 34个月)。除1例患者外,所有患者预后良好。无死亡病例。
创伤性儿童PFEDH较为罕见。在决定是否手术前,需要评估患者的临床状况和血肿体积。大多数病例伴有枕骨骨折,约一半伴有幕上扩展;术前需仔细评估。由于相邻静脉窦破裂,汹涌的静脉出血可能是一个主要问题。鉴于手术清除的阈值较低,及时干预对于取得良好预后至关重要。虽然并非创新性研究,但这是第二大病例系列,提供了更多数据,并为儿科患者此类病变的现有文献做出了贡献。