Moon Myung-Sang, Kim Sung-Soo, Lee Bong-Jin, Moon Jeong-Lim, Lin Jin-Fu, Moon Young-Wan
Department of Orthopaedic Surgery, Cheju Halla General Hospital, Jeju, Korea.
J Orthop Surg (Hong Kong). 2010 Aug;18(2):143-7. doi: 10.1177/230949901001800203.
To evaluate the morphologies of congenital C2-3 synostosis in 25 patients.
Radiographs of 11 males and 14 females aged 5 to 74 years with congenital C2-3 synostosis were reviewed. All cases were found incidentally on radiographs when presenting with neck/shoulder discomfort/pain.
13 of the patients had spondylosis in 21 segments: C1-2 (n=1) and C3-4 (n=1), C4-5 (n=7), C5-6 (n=9), and C6-7 (n=3). Of whom 12 had normal sagittal alignment and one had kyphotic synostosis (who developed compensatory hyperlordosis of the caudal mobile segments and subsequent spondylosis at C3-4 and C5 retrolisthesis). The remaining 12 patients had no spondylosis and had normal sagittal alignment, but had other associated pathologies including disc herniation at C3-4, C1 ring hypoplasia, and calcification of the nuchal ligament.
Normally aligned congenital synostosis of C2-3 is rarely associated with a junctional problem, whereas a kyphotic synostosis is associated with a caudal junctional problem. Spondylosis developing after age 40 years is not associated with C2-3 synostosis.
评估25例先天性C2-3关节融合的形态。
回顾性分析11例男性和14例女性患者的X线片,年龄5至74岁,均为先天性C2-3关节融合。所有病例均在因颈部/肩部不适/疼痛进行X线检查时偶然发现。
13例患者在21个节段出现脊柱退变:C1-2(n = 1)、C3-4(n = 1)、C4-5(n = 7)、C5-6(n = 9)和C6-7(n = 3)。其中12例矢状位排列正常,1例为后凸性关节融合(该患者出现尾侧活动节段代偿性过度前凸,随后C3-4节段发生脊柱退变和C5椎体后滑脱)。其余12例患者无脊柱退变,矢状位排列正常,但存在其他相关病变,包括C3-4椎间盘突出、C1环发育不全和项韧带钙化。
正常排列的先天性C2-3关节融合很少与交界区问题相关,而后凸性关节融合与尾侧交界区问题相关。40岁以后发生的脊柱退变与C2-3关节融合无关。