Ellenbogen R G, Gruss J S, Cunningham M L
Division of Pediatric Neurological Surgery, Seattle Children's Hospital and Regional Medical Center, Seattle, Washington, USA.
Clin Neurosurg. 2000;47:303-18.
There has been an evolution of thought on the diagnosis and treatment of posterior plagiocephaly. Synostotic posterior plagiocephaly (lambdoid synostosis) can be diagnosed and differentiated from non-synostotic posterior plagiocephaly (positional molding) based on specific cosmetic and radiologic criteria. The advent of high-resolution three-dimensional CT analysis of cranial morphology combined with meticulous clinical studies of the two major causes of posterior plagiocephaly has added much to our understanding of this skull deformity. Children with lambdoid synostosis have a trapezoid-shaped skull with posterior displacement of their ipsilateral ear, ipsilateral mastoid bossing, contralateral occipital bossing, and a fused lambdoid suture that appears as a ridge. Children with posterior plagiocephaly without lambdoid synostosis have a characteristic parallelogram-shaped skull with anterior displacement of the ipsilateral ear and ipsilateral frontal bossing. This subject is surrounded in controversy because many of the children in the past thought to have lambdoid synostosis probably did not, based in part on the aforementioned specific criteria. This is an important point, as most patients with posterior plagiocephaly without synostosis will improve without surgery. One should thus be appropriately conservative in the selection of patients for surgery. The majority of infants evaluated at craniofacial clinics presumably have posterior plagiocephaly without synostosis and can be successfully treated with frequent head turning, helmet, or band therapy. Patients with clinically and radiologically proven synostotic posterior plagiocephaly and a severe deformity should undergo craniofacial surgery. The technique of biparieto-occipital craniotomy is safe, simple, and delivers a good cosmetic result. Our postoperative photographic evaluations have shown an immediate, aesthetically pleasing change in the contour of the occiput, which tends to improve with time.
关于后斜头畸形的诊断和治疗,人们的认识一直在不断发展。可以根据特定的外观和放射学标准,诊断并区分骨性连接性后斜头畸形(人字缝早闭)与非骨性连接性后斜头畸形(体位性塑形)。高分辨率三维CT对颅骨形态的分析,以及对后斜头畸形两大主要病因的细致临床研究,极大地增进了我们对这种颅骨畸形的理解。患有人字缝早闭的儿童头颅呈梯形,同侧耳朵向后移位,同侧乳突突出,对侧枕部突出,且融合的人字缝呈现为一条嵴。没有人字缝早闭的后斜头畸形儿童头颅呈特征性的平行四边形,同侧耳朵向前移位,同侧额部突出。这个问题存在争议,因为过去许多被认为有人字缝早闭的儿童可能并非如此,部分原因就在于上述特定标准。这一点很重要,因为大多数非骨性连接性后斜头畸形患者不经手术即可改善。因此,在选择手术患者时应适当保守。在颅面诊所接受评估的大多数婴儿可能患有非骨性连接性后斜头畸形,通过频繁转头、头盔或头带治疗可成功治愈。临床和放射学证实为骨性连接性后斜头畸形且畸形严重的患者应接受颅面手术。双额枕开颅术技术安全、简单,美容效果良好。我们术后的照片评估显示,枕部轮廓立即出现美观的变化,且随着时间推移往往会有所改善。