Department of Orthopedic Surgery, The University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-Ku, Tokyo, 113-8655, Japan.
Surgical Center, The University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-Ku, Tokyo, 113-8655, Japan.
Skeletal Radiol. 2023 Sep;52(9):1785-1789. doi: 10.1007/s00256-023-04297-5. Epub 2023 Feb 11.
Down syndrome, also known as trisomy 21, is associated with congenital cervical spine abnormalities, including atlantoaxial instability with or without os odontoideum, atlanto-occipital instability, and hypoplasia of the atlas. Herein, we report a case of Down syndrome complicated by congenital atlanto-occipital dislocation. The patient presented with severe cervical myelopathy at 13 years of age after a 10-year follow-up. Radiography and computed tomography revealed os odontoideum protruding into the foramen magnum and congenital anterior atlanto-occipital dislocation. Additionally, a bifurcated internal occipital crest with a thinned central portion of the occipital bone was noted. Magnetic resonance imaging revealed kyphotic alignment of the spinal cord with severe compression at the foramen magnum level. As the neurological impairment was partially improved by halo vest immobilization, we performed in situ O-C2 fusion with an iliac autograft and decompression of the foramen magnum and posterior arch of C1. An improvement was observed immediately after surgery. Two years after surgery, radiography and computed tomography showed solid O-C2 segment fusion. The accumulation of similar cases is essential for determining the prognosis or optimal treatment for this rare congenital condition.
唐氏综合征,又称 21 三体综合征,与先天性颈椎异常相关,包括寰枢椎不稳伴或不伴齿状突游离、寰枕不稳和寰椎发育不良。本文报告一例唐氏综合征并发先天性寰枕脱位。患者 13 岁时,经过 10 年随访,出现严重的颈髓病变。影像学检查显示齿状突突入颅后窝,先天性寰枕前脱位。此外,还可见分叉的枕内嵴,伴有枕骨中部变薄。磁共振成像显示颈椎呈后凸排列,在颅后窝水平严重受压。由于 halo 背心固定术使神经功能缺损部分改善,我们进行了原位寰枢椎融合术,取自体髂骨,并进行颅后窝和 C1 后弓减压。术后即刻观察到改善。术后 2 年,影像学检查显示寰枢椎融合稳定。此类病例的积累对于确定这种罕见先天性疾病的预后或最佳治疗方法至关重要。