Congenital atlanto-occipital dislocation in a patient with Down syndrome: a case report

被引:2
作者
Onodera, Ryoko [1 ]
Sakamoto, Ryuji [1 ]
Taniguchi, Yuki [1 ,2 ]
Hirai, Shima [1 ]
Matsubayashi, Yoshitaka [1 ]
Kato, So [1 ]
Oshima, Yasushi [1 ]
Tanaka, Sakae [1 ]
机构
[1] Univ Tokyo Hosp, Dept Orthoped Surg, 7-3-1 Hongo,Bunkyo Ku, Tokyo 1138655, Japan
[2] Univ Tokyo Hosp, Surg Ctr, 7-3-1 Hongo,Bunkyo Ku, Tokyo 1138655, Japan
关键词
Atlanto-occipital dislocation; Os odontoideum; Down syndrome; Basilar invagination; Bifurcated internal occipital crest; INSTABILITY;
D O I
10.1007/s00256-023-04297-5
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
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.
引用
收藏
页码:1785 / 1789
页数:5
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