Department of Cranio-Maxillofacial Surgery, University Hospital Basel, University of Basel, Switzerland.
J Neurosurg. 2011 Sep;115(3):528-35. doi: 10.3171/2011.3.JNS101517. Epub 2011 Apr 15.
Craniometaphyseal dysplasia is an extremely rare, genetic bone-remodeling disorder. Comparable to osteopetrosis, fibrous dysplasia, and other infrequent conditions, craniometaphyseal dysplasia is characterized by progressive diffuse hyperostosis of the neuro- and viscerocranium. Affected patients present with a pathognomonic dysmorphia: macrocephalus, hypertelorism, bulky facial skeleton, and a prominent mandible. Progressive thickening and petrification of the craniofacial bones can continue throughout life, often resulting in neurological symptoms due to obstruction of the cranial nerves in the foramina and therefore immediately requiring neurosurgical interventions to avoid persistent symptoms with severe impairment of function. Treatment is largely infeasible given the lack of suitable tools to perform a craniotomy through the gross calvarial bone. In this paper, the authors present a complete process chain from the CT-based generation of an individual patient's model displaying his pathology to optimized preoperative planning of the skull's shape with a thickness of about 6-7 mm. For concise verification of the surgical plan in an operating room environment, a 3D real-time navigation prototype system was utilized. To guarantee realization of the surgery in a reasonable time frame, the mechanical tools were preoperatively selected for optimizing the ablation rate in porcine and bovine bone, which were comparable to that in the patient. This process chain was developed in a modular way, so that it could be easily adopted completely or partially for other surgical indications. A 21-year-old man was treated according to this sophisticated concept. Skull bone more than 50 mm thick in some regions was reduced to physiological thickness. The patient was thus in a stage that neurosurgical interventions could be performed with a regular risk within a reasonable time of treatment.
颅骨骨干发育不良是一种极其罕见的遗传性骨重塑疾病。与骨质硬化症、纤维结构不良等罕见疾病类似,颅骨骨干发育不良的特征是神经和内脏颅面骨进行性弥漫性过度骨化。受影响的患者表现出一种特有的畸形:大头畸形、眼球突出、宽大的面颅骨和突出的下颌骨。颅面骨的进行性增厚和石化可贯穿整个生命周期,由于颅神经在孔中受阻,常导致神经症状,因此需要立即进行神经外科干预,以避免因功能严重受损而持续出现症状。由于缺乏通过大体颅骨进行开颅术的合适工具,因此治疗在很大程度上不可行。本文作者提出了一个完整的流程链,从基于 CT 的患者个体模型生成开始,该模型显示了患者的病理情况,然后优化颅骨形状的术前规划,厚度约为 6-7 毫米。为了在手术室环境中简洁地验证手术计划,使用了一个 3D 实时导航原型系统。为了保证在合理的时间框架内完成手术,术前选择了机械工具来优化猪和牛骨中的消融率,使其与患者的消融率相当。该流程链以模块化的方式开发,因此可以轻松地完全或部分采用,用于其他手术适应证。一名 21 岁的男性患者按照这一复杂的概念进行了治疗。颅骨的某些区域厚度超过 50 毫米,被减少到生理厚度。因此,患者处于可以在合理的治疗时间内,以常规风险进行神经外科干预的阶段。