Weinzweig Jeffrey, Baker Stephen B, Whitaker Linton A, Sutton Leslie N, Bartlett Scott P
Department of Surgery, Brown University School of Medicine, Rhode Island Hospital, Providence, USA.
Plast Reconstr Surg. 2002 Aug;110(2):397-408. doi: 10.1097/00006534-200208000-00003.
An algorithm for the management of sagittal synostosis in older children who underwent delayed cranial vault reconstruction is presented. This algorithm tailors the surgical approach to the specific craniofacial deformity present in each case. The scaphocephalic deformity characteristic of sagittal synostosis varies significantly when presentation is delayed beyond the first year of life, the time during which reconstruction is usually performed. Sixteen patients with sagittal synostosis who presented after 12 months of age, and were a mean of 3.2 years of age at the time of cranial vault reconstruction, were reviewed. Four patients demonstrated preoperative symptoms and objective findings indicative of increased intracranial pressure, including frequent headaches and emesis, papilledema, or digital markings on computed tomographic scan. Each of the 16 patients underwent either (1) single-stage total vault reconstruction with or without concomitant fronto-orbital expansion; (2) two-stage total vault reconstruction with anterior two-thirds vault expansion followed by transverse occipital expansion and recession a mean of 8.7 months later; or (3) anterior two-thirds vault reconstruction with or without fronto-orbital expansion. In each case, the extent of the scaphocephalic deformity determined the procedure used. The presence of severe frontal bossing associated with transverse restriction of the orbitotemporal region was an indication for fronto-orbital expansion in addition to vault reconstruction, whereas significant occipital protrusion was an indication for transverse posterior vault expansion and recession in addition to anterior two-thirds vault reconstruction. Excellent aesthetic results were obtained in all cases regardless of the type of reconstruction performed. However, it is essential that the extent of the deformity be carefully evaluated preoperatively to permit selection of the appropriate technique for reconstruction.
本文介绍了一种针对大龄儿童矢状缝早闭并接受延迟性颅骨穹窿重建术的管理算法。该算法根据每个病例中存在的特定颅面畸形来调整手术方式。矢状缝早闭的舟状头畸形特征在出生后第一年(通常进行重建的时间)之后出现延迟时会有显著变化。回顾了16例12个月龄后出现矢状缝早闭且在颅骨穹窿重建时平均年龄为3.2岁的患者。4例患者术前有提示颅内压升高的症状和客观体征,包括频繁头痛和呕吐、视乳头水肿或计算机断层扫描上的指压痕。16例患者均接受了以下手术之一:(1)一期全颅骨穹窿重建术,可伴有或不伴有额眶扩张;(2)两期全颅骨穹窿重建术,先进行前三分之二颅骨穹窿扩张,平均8.7个月后再进行枕部横向扩张和后缩;或(3)前三分之二颅骨穹窿重建术,可伴有或不伴有额眶扩张。在每种情况下,舟状头畸形的程度决定了所采用的手术方式。除了颅骨穹窿重建外,伴有眶颞区横向受限的严重额部隆起是进行额眶扩张的指征,而明显的枕部突出是除了前三分之二颅骨穹窿重建外进行枕部后外侧穹窿扩张和后缩的指征。无论进行何种类型的重建,所有病例均获得了良好的美学效果。然而,术前必须仔细评估畸形的程度,以便选择合适的重建技术。