Foulkes G D, Reinker K
Division of Orthopaedics, John A. Burns School of Medicine, University of Hawaii, Honolulu.
J Pediatr Orthop. 1994 Mar-Apr;14(2):242-8. doi: 10.1097/01241398-199403000-00021.
Seventy-one cases of congenital constriction band syndrome (CCBS) were reviewed. The year of birth, sex, ethnic background, gestational history, family history, and concurrent diagnoses were obtained. The anatomic patterns of involvement, degree of impairment, and number and type of surgical interventions were recorded. The incidence of CCBS appears to be rising. The average patient had three involved limbs, with a predilection for distal, central digits of the upper extremity. Abnormal gestational histories were found in 60% of the cases; 50% had concurrent diagnoses, and nearly one-third had club-feet. The average patient had a 20% whole body impairment and required three reconstructive procedures. Distraction osteogenesis and free osteocutaneous transfer were useful. We feel that the term "early amnion rupture sequence" more accurately reflects the true pathogenesis of CCBS.
回顾了71例先天性束带综合征(CCBS)病例。获取了出生年份、性别、种族背景、妊娠史、家族史和并发诊断情况。记录了受累的解剖模式、损伤程度以及手术干预的次数和类型。CCBS的发病率似乎在上升。平均每位患者有三个肢体受累,以上肢远端、中间手指为好发部位。60%的病例有异常妊娠史;50%有并发诊断,近三分之一有马蹄内翻足。平均每位患者有20%的全身损伤,需要进行三次重建手术。牵张成骨术和游离骨皮瓣移植很有用。我们认为“早期羊膜破裂序列征”这一术语更准确地反映了CCBS的真正发病机制。