Searle Clark P, Hildebrand Randall K, Lester Edward L, Caskey Paul M
Madigan Army Medical Center, Tacoma, Washington, USA.
J Pediatr Orthop B. 2004 May;13(3):184-8. doi: 10.1097/00009957-200405000-00008.
We have noted a number of patients with features of fibular hemimelia with radiographically normal fibulae. This study was undertaken to further define this group. A review of hospital records and radiographs over a 72-year period identified 149 limbs in 123 patients with features of fibular hemimelia syndrome. Sixteen limbs in fourteen patients had findings of fibular hemimelia with radiographically normal fibulae. Thirteen of 16 had absent lateral rays with either ball and socket ankle joint, tarsal coalition or both. Six of the 13 had limb shortening. Three limbs in three patients did not have absent lateral rays, but had at least two other features of fibular hemimelia syndrome. All of these three limbs had ball and socket ankles and tarsal coalitions and two had shortening. These patients represent a mild subset of fibular hemimelia syndrome and we propose that they be classified as type 0 fibular hemimelia.
我们注意到一些患有腓骨半侧畸形特征但X线片显示腓骨正常的患者。开展本研究以进一步明确这一群体。回顾72年间的医院记录和X线片,在123例患有腓骨半侧畸形综合征特征的患者中确定了149条肢体。14例患者的16条肢体有腓骨半侧畸形的表现且X线片显示腓骨正常。16例中的13例外侧射线缺如,伴有球窝踝关节、跗骨联合或两者皆有。13例中的6例有肢体短缩。3例患者的3条肢体没有外侧射线缺如,但有至少另外两项腓骨半侧畸形综合征的特征。这3条肢体均有球窝踝关节和跗骨联合,其中2条有短缩。这些患者代表了腓骨半侧畸形综合征的一个轻度亚组,我们建议将他们分类为0型腓骨半侧畸形。