Marchac D, Renier D, Broumand S
Craniofacial Unit, Hôpital Necker-Enfants Malades, Paris, France.
Br J Plast Surg. 1994 Jun;47(4):211-22. doi: 10.1016/0007-1226(94)90001-9.
The timing of surgery for craniosynostosis is still controversial. Having used the same basic techniques since 1973, and having done follow-up on the growth of our 983 operated patients, we thought it useful to report our protocol. Early frontocranial remodelling is performed between 2 and 4 months for brachycephalies, but the other craniosynostoses are operated on between 6 and 12 months of age. When diagnosis is made later, we perform the same operations until 4 years of age, with some modifications, such as a tongue in groove advancement for brachycephalies, and a complete closure of the bony defects after 2 years of age. Later on, facial distortion and frontal sinus development complicate the surgery. For syndromal craniofacial synostosis, we prefer to perform a two-step operation: forehead advancement first, facial advancement later, to avoid the risk of frontal osteitis. The frontofacial monobloc is indicated, in our opinion, for severe exorbitism in infancy but otherwise we prefer a two-stage procedure. Facial bipartition is necessary to narrow the upper face and widen the maxilla in Apert's syndrome.
颅骨缝早闭的手术时机仍存在争议。自1973年以来我们一直采用相同的基本技术,并对983例接受手术的患者的生长情况进行了随访,我们认为报告我们的方案是有用的。短头畸形在2至4个月大时进行早期额颅重塑,但其他颅骨缝早闭在6至12个月大时进行手术。如果诊断较晚,我们在4岁之前进行相同的手术,但会有一些调整,例如短头畸形采用榫槽推进术,2岁后完全闭合骨缺损。后期,面部畸形和额窦发育会使手术复杂化。对于综合征性颅面骨缝早闭,我们倾向于分两步进行手术:先进行前额前移,之后进行面部前移,以避免额骨炎的风险。在我们看来,婴幼儿期严重眼球突出时可采用颅面整块前移术,否则我们更倾向于分两阶段进行手术。在Apert综合征中,面部二分术对于缩小上面部和扩宽上颌骨是必要的。