Department of Pediatrics, Hospital of Neuchâtel, Neuchâtel, Switzerland.
Department Woman-Mother-Child, Division of Pediatrics, University Hospital of Lausanne, Lausanne, Switzerland.
BMC Pediatr. 2020 Feb 19;20(1):77. doi: 10.1186/s12887-020-1957-x.
Spinal epidural hematoma without significant trauma is a rare condition with potentially severe outcome. This case report and systematic review of the literature illustrates the clinical presentation, risk factors, evaluation, treatment and outcomes of spinal epidural hematoma without significant trauma in children.
We report one case of a 7-year-old girl who developed a neck pain after minor cervical sprain. MRI showed a right posterior epidural hematoma extending from C2/3 to T1. The hematoma was surgically evacuated, and the histopathology showed an arteriovenous malformation. Postoperative MRI showed complete evacuation of the hematoma and no residual vascular malformation. We report a second ASE with idiopathic spinal epidural hematoma of a 4½-year-old boy presenting with neck pain. MRI showed a right-sided latero-posterior subacute spinal epidural hematoma at C3-C5. Owing to the absence of any neurological deficit, the patient was treated conservatively. MRI at 3 months showed complete resolution of the hematoma.
Spinal epidural hematoma without significant trauma in children is a rare condition. It may present with unspecific symptoms. Screening for bleeding diathesis is warranted and neuroradiologic follow-up is essential to rule out vascular malformation. Whereas most children have a favorable outcome, some do not recover, and neurological follow-up is required.
无明显外伤的脊柱硬膜外血肿是一种罕见的疾病,可能导致严重后果。本病例报告和文献系统回顾说明了儿童无明显外伤的脊柱硬膜外血肿的临床表现、危险因素、评估、治疗和结局。
我们报告了一例 7 岁女孩,在轻微颈椎扭伤后出现颈部疼痛。MRI 显示 C2/3 至 T1 右侧硬膜外血肿。血肿行手术清除,组织病理学显示动静脉畸形。术后 MRI 显示血肿完全清除,无残留血管畸形。我们报告了第二例 ASE,为 4 岁半的男孩,无明显外伤,表现为颈部疼痛。MRI 显示 C3-C5 右侧旁后急性硬膜外血肿。由于无任何神经功能缺损,患者接受保守治疗。3 个月时的 MRI 显示血肿完全吸收。
儿童无明显外伤的脊柱硬膜外血肿是一种罕见疾病。它可能表现为非特异性症状。需要筛查出血性疾病,神经影像学随访是排除血管畸形所必需的。虽然大多数儿童预后良好,但有些儿童无法恢复,需要进行神经随访。