Kalliainen Loree K, Drake David B, Edgerton Milton T, Grzeskiewicz Joseph L, Morgan Raymond F
Ohio State University, Columbus, USA.
Ann Plast Surg. 2003 May;50(5):456-62; discussion 463-70. doi: 10.1097/01.SAP.0000044149.76364.D4.
Freeman-Sheldon syndrome is a rare form of distal arthrogryposis characterized by craniofacial anomalies, a rheumatoid-appearing hand, and pedal deformities. The hand deformities include ulnar deviation of the fingers, camptodactyly, first web space contracture, and hypoplasia of the thumb. Because of clinical variability and rarity, there is no standard management protocol. The authors have developed a systematic method of management of the hand in Freeman-Sheldon syndrome using principles commonly applied to other complex hand problems. In 17 years, the authors have evaluated nine patients. Of 18 hands evaluated, the authors have operated on 15. Good results were achieved in five hands and fair results in 10. There were no cases of useless hands. The authors have been most pleased with the results after crossed intrinsic transfers, centralization of extensor tendons, and intrinsic release of the thumb. Although physical deformities remain, functional adaptation is generally good.
弗里曼-谢尔顿综合征是一种罕见的远端关节挛缩症,其特征为颅面畸形、类似类风湿关节炎的手部表现以及足部畸形。手部畸形包括手指尺偏、屈曲指、第一掌骨间隙挛缩和拇指发育不全。由于临床变异性和罕见性,尚无标准的治疗方案。作者采用常用于其他复杂手部问题的原则,制定了一种弗里曼-谢尔顿综合征手部的系统治疗方法。在17年里,作者评估了9例患者。在评估的18只手中,作者对15只进行了手术。5只手取得了良好效果,10只手取得了尚可的效果。没有出现无用手的病例。作者对交叉固有肌转移、伸肌腱中心化和拇指固有肌松解术后的结果最为满意。虽然身体畸形仍然存在,但功能适应性总体良好。