Gabay Segev, Hausman-Kedem Moran, Sadeh Gonik Udi, Jonash-Kimchi Tali, Shiran Shelly, Chapot Rene, Roth Jonathan, Lidar Zvi, Ofir Dror
Department of Pediatric Neurosurgery and Pediatric Brain Institute, Dana Dwek Children Hospital, Tel Aviv Medical Center, Tel Aviv, Israel.
Department of Neurosurgery, Spine Surgery Unit, Tel Aviv Medical Center, Tel Aviv University, Tel Aviv, Israel.
Spinal Cord Ser Cases. 2024 Dec 11;10(1):80. doi: 10.1038/s41394-024-00691-w.
Spinal cord arteriovenous malformations (SCAVM) are rare congenital vascular malformations, characterized by two or more AVMs affecting any of the spinal segments. SCAVM has complex pathophysiology and may be associated with acute, or progressively neurological deficits.
A 12-year old girl, presented with progressive neurologic deficits secondary to compressive cervical myelopathy due to a cervical metameric SCAVM. She was successfully treated with a staged surgical-endovascular approach and regained normal neurological function with radiological stability.
SCAVM is a rare disease with complex management, and in many cases, the treatment is focused on palliative care. With multimodality management, of a combined surgical-endovascular approach, the patient achieved neurological, functional, and structural stability over the follow-up period.
脊髓动静脉畸形（SCAVM）是一种罕见的先天性血管畸形，其特征是两个或更多的动静脉畸形影响任何脊髓节段。SCAVM具有复杂的病理生理学，可能与急性或进行性神经功能缺损有关。
一名12岁女孩，因颈椎节段性SCAVM导致压迫性颈髓病继发进行性神经功能缺损。她通过分期手术-血管内治疗方法成功治疗，并在影像学稳定的情况下恢复了正常神经功能。
SCAVM是一种罕见疾病，治疗复杂，在许多情况下，治疗侧重于姑息治疗。通过手术-血管内联合的多模式管理，患者在随访期间实现了神经、功能和结构的稳定。
