Denadai Rafael, Raposo-Amaral Cesar Augusto, Marques Frederico Figueiredo, Ghizoni Enrico, Buzzo Celso Luiz, Raposo-Amaral Cassio Eduardo
From the *Institute of Plastic and Craniofacial Surgery, SOBRAPAR Hospital, Campinas; and †Division of Pediatric Neurosurgery, Department of Neurology, School of Medical Sciences, State University of Campinas (UNICAMP), Campinas, São Paulo, Brazil.
Ann Plast Surg. 2016 Aug;77(2):195-200. doi: 10.1097/SAP.0000000000000640.
The surgical management of craniofacial fibrous dysplasia is controversial. The purpose of this study was to report the surgical outcomes of individualized management of craniofacial fibrous dysplasia of a single institution.
Data from patients (n = 20) with craniofacial fibrous dysplasia, who were surgically treated between 2007 and 2014, were analyzed. Surgical approach (radical or conservative surgery) was individualized according to age, craniofacial anatomical site (zones I to IV of Chen and Noordhoff), functional issues, aesthetic impairment, patients/parents' preferences, and surgical team experience. The surgical outcomes (radical surgery group versus conservative surgery group) were compared based on the age at the time of the procedure, the length of hospital stay, reoperation, recurrence and complication rates, and the Whitaker grading system.
Significant (all P < 0.05) differences were observed in patients with craniofacial fibrous dysplasia who were treated with radical excision (65%) compared with those treated with limited reduction burring (35%), according to age (19.22 years versus 12.57 years), the length of hospital stay (3.56 days versus 1.29 days), recurrence (15% versus 71%), and number of subsequent procedures (1 intervention versus 2.4 interventions), respectively. The radical surgery group presented a significantly (P < 0.05) lower initial Whitaker outcome score than the conservative surgery group (1.89 and 2.57, respectively). Similar (all P > 0.05) final Whitaker outcome scores (1.56 versus 1.71) and surgical complication rates (11% versus 14%) were recorded between the treatment groups.
Based on clinical experience and surgical outcomes presented in this study, the surgical approach of craniofacial fibrous dysplasia should be tailored to individual patient's needs.
颅面部骨纤维异常增殖症的外科治疗存在争议。本研究旨在报告一家机构对颅面部骨纤维异常增殖症进行个体化治疗的手术结果。
分析2007年至2014年间接受手术治疗的20例颅面部骨纤维异常增殖症患者的数据。手术方式(根治性手术或保守性手术)根据年龄、颅面部解剖部位(Chen和Noordhoff的I至IV区)、功能问题、美观损害、患者/家长的偏好以及手术团队经验进行个体化选择。根据手术时的年龄、住院时间、再次手术情况、复发率和并发症发生率以及惠特克分级系统,比较手术结果(根治性手术组与保守性手术组)。
与采用有限磨除术治疗的患者(35%)相比,接受根治性切除术治疗的颅面部骨纤维异常增殖症患者在年龄(19.22岁对12.57岁)、住院时间(3.56天对1.29天)、复发率(15%对71%)和后续手术次数(1次干预对2.4次干预)方面存在显著差异(所有P<0.05)。根治性手术组的初始惠特克结果评分显著低于保守性手术组(分别为1.89和2.57,P<0.05)。两组治疗后的最终惠特克结果评分(1.56对1.71)和手术并发症发生率(11%对14%)相似(所有P>0.05)。
基于本研究中的临床经验和手术结果,颅面部骨纤维异常增殖症的手术方式应根据患者个体需求进行调整。