Service de chirurgie craniomaxillofaciale et stomatologie, hôpital Trousseau, CHU de Tours, 37000 Tours, France; Université François-Rabelais, 37000 Tours, France.
Service de chirurgie craniomaxillofaciale et stomatologie, hôpital Trousseau, CHU de Tours, 37000 Tours, France; Université François-Rabelais, 37000 Tours, France.
J Stomatol Oral Maxillofac Surg. 2017 Oct;118(5):310-312. doi: 10.1016/j.jormas.2017.06.001. Epub 2017 Jun 12.
Fronto-metaphyseal dysplasia (FMD), also called Gorlin-Cohen syndrome, is a rare syndrome initially described in 1969 by Gorlin and Cohen. Patients present skeletal dysplasia, craniofacial malformations and digit abnormalities. Craniofacial phenotype of FMD is characterized by supraorbital hyperostosis, hypertelorism, down-slanting palpebral fissures, broad nasal bridge and micrognathia. Here, we report the first adult case of craniofacial reconstruction with frontal cranioplasty in a patient with FMD.
A 21-year-old male patient presented with aesthetic requests related to his facial abnormalities. The patient underwent a fronto-orbital cranioplasty using a coronal approach. Orbital, frontal and nasal hyperostoses were contoured in order to obtain a symmetric result. The patient had no postoperative complication. Aesthetic results were satisfactory and stable after 6 months of follow-up.
The density and the quality of craniofacial bones were normal and this may account for the stability of cranioplasty results over time. Because bone was normal, cranioplasty is safety and stable in FMD.
额-面骨发育不良(FMD),又称 Gorlin-Cohen 综合征,是一种罕见的综合征,最初由 Gorlin 和 Cohen 于 1969 年描述。患者表现为骨骼发育不良、颅面畸形和指(趾)异常。FMD 的颅面表型特征为眶上嵴骨过度生长、眼距过宽、睑裂下斜、宽鼻桥和小下颌。在此,我们报告首例 FMD 患者行额骨颅骨成形术的颅面重建的成年病例。
一名 21 岁男性患者因面部畸形提出美容诉求。患者采用冠状切口行额眶颅面骨切除术。为获得对称效果,对眶、额和鼻骨的过度生长进行了整形。患者术后无并发症。随访 6 个月后,美容效果满意且稳定。
颅面骨的密度和质量正常,这可能是颅骨成形术结果随时间推移稳定的原因。由于骨质正常,FMD 患者的颅骨成形术是安全且稳定的。