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克鲁宗综合征:基于CT扫描对呈现的畸形及手术结果进行定量评估

Crouzon syndrome: quantitative assessment of presenting deformity and surgical results based on CT scans.

作者信息

Posnick J C, Lin K Y, Jhawar B J, Armstrong D

机构信息

Department of Surgery, Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

Plast Reconstr Surg. 1993 Nov;92(6):1027-37.

PMID:8234498
Abstract

We reviewed our experience with 14 children who presented sequentially with untreated Crouzon syndrome and whose cranial vault presentation was with bilateral coronal synostosis. Using a method of 14 measurements in the cranio-orbitozygomatic region taken from preoperative and postoperative CT scans in these patients, we documented their presenting skeletal morphology and the results of surgical correction at least 1 year after operation. Our preoperative measurements confirmed a widened anterior cranial vault at 108 percent of normal and a cranial length averaging only 92 percent of normal. In comparison with age-matched controls, orbital measurements revealed a widened anterior interorbital distance at 122 percent of normal, an increased intertemporal width at 121 percent of normal, globe protrusion at 119 percent of normal, and a short medial orbital wall distance at only 86 percent of normal. The distance between the zygomatic buttresses and the interarch distance were found to be increased at 106 and 103 percent of normal, respectively. The zygomatic arch lengths were substantially shortened at only 87 percent of age-matched control values. These findings confirmed clinical observations of brachycephalic anterior cranial vaults with shallow, hyperteloric orbits and globe proptosis. Generally, in these patients the midface is horizontally retrusive and transversely wide, reflected in wide and shortened zygomas. Assessment of the postoperative results at least 1 year later showed no significant changes in any craniofacial measurements. Our findings indicate that early surgical attempts to decompress and reshape the cranio-orbital regions may limit the effects of increased intracranial pressure but do not correct the deformity as judged by CT scan evaluation at least 1 year later. Over the period of the study, the Crouzon deformity did not worsen after surgery, but the measurements remained far from normal.

摘要

我们回顾了14例先后就诊的未经治疗的克鲁宗综合征患儿的病例,这些患儿的颅顶表现为双侧冠状缝早闭。我们采用一种方法,对这些患者术前和术后CT扫描的颅眶颧区域进行14项测量,记录了他们术前的骨骼形态以及术后至少1年的手术矫正结果。我们的术前测量结果证实,前颅顶增宽至正常的108%,颅长平均仅为正常的92%。与年龄匹配的对照组相比,眼眶测量显示,眶间前距离增宽至正常的122%,颞间宽度增加至正常的121%,眼球突出至正常的119%,眶内侧壁距离缩短至正常的86%。发现颧弓支柱之间的距离和牙弓间距离分别增加至正常的106%和103%。颧弓长度大幅缩短,仅为年龄匹配对照组值的87%。这些发现证实了临床观察到的短头型前颅顶、浅而眼距过宽的眼眶和眼球突出的情况。一般来说,在这些患者中,中面部水平后缩且横向增宽,表现为颧骨变宽和缩短。至少1年后对术后结果的评估显示,任何颅面测量值均无显著变化。我们的研究结果表明,早期手术尝试对颅眶区域进行减压和重塑可能会限制颅内压升高的影响,但至少1年后通过CT扫描评估发现,手术并未纠正畸形。在研究期间,克鲁宗畸形术后未恶化,但测量值仍远未恢复正常。

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