Tsirikos Athanasios I, McMaster Michael J
Scottish National Spine Deformity Center, Royal Hospital for Sick Children (Level 5), Sciennes Road, Edinburgh EH9 1LF, United Kingdom.
J Bone Joint Surg Am. 2005 Nov;87(11):2523-36. doi: 10.2106/JBJS.D.02654.
Congenital anomalies of the ribs and chest wall as well as Sprengel deformity of the shoulder are often associated with congenital deformities of the spine. It has been suggested that rib anomalies may adversely affect the progression of the spinal deformity.
We conducted a retrospective study of the medical records and spine radiographs of 620 consecutive patients with congenital deformities of the spine; 497 patients (80%) had scoliosis; eighty-eight patients (14%), kyphoscoliosis; and thirty-five patients (6%), kyphosis. The rib anomalies were classified into simple and complex, and the presence of a Sprengel deformity of the shoulder was recorded. The rate of scoliosis deterioration without treatment before the age of eleven years, as well as the patient age and curve size at the time of surgery, was compared for different types of vertebral abnormalities in patients with and without rib anomalies.
A total of 119 patients (19.2%) had rib anomalies, which were most commonly associated with congenital scoliosis (111 patients; 93%) and were much less frequently associated with congenital kyphoscoliosis or kyphosis (eight patients). The rib anomalies were simple in ninety-five patients and complex in twenty-four. Eighty-five patients (71%) with rib abnormalities had a scoliosis due to a unilateral failure of vertebral segmentation, and seven patients had mixed or unclassifiable vertebral anomalies. In contrast, only sixteen of 203 patients with a scoliosis due to a hemivertebra alone had rib anomalies. The rib anomalies were most frequently associated with a thoracic or thoracolumbar scoliosis (102 patients; 92%) and occurred on the concavity in eighty-two patients (74%), the convexity in twenty-two patients (20%), and were bilateral in seven patients. The Sprengel deformity occurred in forty-five patients and most frequently in association with a thoracic scoliosis due to a unilateral failure of vertebral segmentation (twenty-seven patients). No significant difference was detected in the rate of curve progression without treatment in patients with and without rib anomalies. The only exception was the mean age at the time of surgery, which was higher for patients with a unilateral unsegmented bar without rib anomalies (p = 0.005). In addition, no significant difference was found with regard to any tethering effect due to the site of the rib fusions on the concavity of the scoliosis, i.e., whether they were in close approximation to the spine or were more lateral (p > 0.05).
Congenital rib anomalies occur most commonly on the concavity of a thoracic or thoracolumbar congenital scoliosis that is due to a unilateral failure of vertebral segmentation, and they do not appear to have an adverse effect on curve size or rate of progression.
肋骨和胸壁的先天性畸形以及肩部的先天性高肩胛症常与脊柱的先天性畸形相关。有人提出肋骨异常可能会对脊柱畸形的进展产生不利影响。
我们对620例连续性脊柱先天性畸形患者的病历和脊柱X光片进行了回顾性研究;497例患者(80%)患有脊柱侧弯;88例患者(14%)患有脊柱后凸侧弯;35例患者(6%)患有脊柱后凸。肋骨异常被分为简单型和复杂型,并记录是否存在肩部先天性高肩胛症。比较了11岁前未经治疗的脊柱侧弯恶化率,以及有肋骨异常和无肋骨异常患者在手术时的年龄和侧弯度数。
共有119例患者(19.2%)存在肋骨异常,最常见于先天性脊柱侧弯(111例患者;93%),而与先天性脊柱后凸侧弯或脊柱后凸的关联则少得多(8例患者)。95例患者的肋骨异常为简单型,24例为复杂型。85例(71%)有肋骨异常的患者因单侧椎体分节不全导致脊柱侧弯,7例患者有混合型或无法分类的椎体异常。相比之下,仅因半椎体导致脊柱侧弯的203例患者中,只有16例有肋骨异常。肋骨异常最常与胸段或胸腰段脊柱侧弯相关(102例患者;92%),82例患者(74%)发生在凹侧,22例患者(20%)发生在凸侧,7例患者为双侧。先天性高肩胛症发生在45例患者中,最常见于因单侧椎体分节不全导致的胸段脊柱侧弯(27例患者)。有肋骨异常和无肋骨异常患者未经治疗时的侧弯进展率无显著差异。唯一的例外是手术时的平均年龄,无肋骨异常的单侧未分节骨桥患者的平均年龄更高(p = 0.005)。此外,关于肋骨融合部位对脊柱侧弯凹侧的任何牵拉效应,即肋骨融合部位是靠近脊柱还是更靠外侧,未发现显著差异(p > 0.05)。
先天性肋骨异常最常发生在因单侧椎体分节不全导致的胸段或胸腰段先天性脊柱侧弯的凹侧,似乎对侧弯度数或进展速度没有不利影响。