Medical College of Wisconsin.
Department of Plastic Surgery, Children's Wisconsin, Medical College of Wisconsin.
J Craniofac Surg. 2021 Sep 1;32(6):2110-2113. doi: 10.1097/SCS.0000000000007401.
The presenting report describes the use of a posterior cranial vault distraction procedure in resolving a Chiari malformation with associated syringomyelia following a surgically-treated nonsyndromic craniosynostosis. Chiari malformations are typically treated with posterior fossa decompression with or without expansion duraplasty. The objective of this report is to describe the effectiveness in resolving both Chiari malformation and secondary syringomyelia with posterior cranial vault distraction osteogenesis. A 5-year-old male, with a history of surgery for sagittal synostosis during infancy, presented with daily severe headaches and dysesthesias in the hands and feet. Imaging demonstrated a copper-beaten calvarium and a Chiari 1 malformation with a 7 mm diameter C4-T1 syrinx. He underwent posterior cranial vault distraction osteogenesis over 3 months to increase his intracranial volume. The patients' headaches improved significantly, and his dysesthesias resolved postoperatively. A magnetic resonance imaging performed 7 months after completion of distraction demonstrated resolution of the Chiari malformation and decompression of his syrinx. A computed tomography scan at 9 months postdistraction showed resolution of the copper-beaten calvarium. Patients with a history of craniosynostosis can develop inadequate cranial volume over time due to abnormal skull growth, leading to secondary Chiari malformation with or without syringomyelia. Posterior vault distraction is an effective strategy to address these conditions and can be employed later in childhood to treat the underlying pathology. The mechanism potentially expands both calvarium and dura, which in turn addresses both the Chiari malformation and secondary syringomyelia.
本报告介绍了在后颅窝骨穹窿牵张术治疗颅缝早闭术后非综合征性颅缝早闭相关 Chiari 畸形伴脊髓空洞症中的应用。Chiari 畸形通常采用后颅窝减压术治疗,或在此基础上进行硬脑膜扩张术。本报告的目的是描述后颅窝骨穹窿牵张成骨术治疗 Chiari 畸形和继发性脊髓空洞症的有效性。一名 5 岁男性,有婴儿期矢状缝早闭手术史,表现为每日严重头痛和手足感觉异常。影像学检查显示颅骨铜斑样外观和 Chiari 1 畸形,伴有直径 7mm 的 C4-T1 脊髓空洞。他接受了 3 个月的后颅窝骨穹窿牵张术,以增加颅内体积。患者头痛明显改善,术后感觉异常消失。完成牵张术后 7 个月行磁共振成像显示 Chiari 畸形缓解,脊髓空洞减压。牵张术后 9 个月行 CT 扫描显示铜斑样颅骨消失。有颅缝早闭病史的患者由于颅骨生长异常,可能会随着时间的推移出现颅内体积不足,导致 Chiari 畸形和/或脊髓空洞症。后颅窝骨穹窿牵张术是解决这些问题的有效策略,可以在儿童后期用于治疗潜在的病理问题。其潜在的机制是同时扩张颅骨和硬脑膜,从而解决 Chiari 畸形和继发性脊髓空洞症。