Lesavoy Malcolm A, Nguyen Dat T, Yospur Gerald, Dickinson Brian P
Division of Plastic & Reconstructive Surgery, UCLA School of Medicine, 16311 Ventura Blvd, Suite 550, Encino CA 91426-4314, USA.
J Craniofac Surg. 2009 Nov;20(6):2251-6. doi: 10.1097/SCS.0b013e3181bfc3a7.
: Encephaloceles are an extension or protrusion of any intracranial matter through a cranial bone defect. The sphenoethmoidal encephalocele is often fatal. For those who survive long enough, expeditious repair is critical. We report a case that was repaired successfully via a combined transcranial and transpalatal approach, and because of successful repair, the patient underwent multiple secondary reconstructions resulting in a 25-year follow-up.
: A 3960-g, term male infant from a normal gestation was delivered via cesarean delivery for breech position. Initial examination revealed a 2 x 3-cm gray intraoral nasopharyngeal mass with smooth mucosal covering extruding through a midline palatal cleft. At 4 weeks of life, extradural and intradural exploration of the encephalocele was performed via a bifrontal craniotomy. At 15 months of age, the patient underwent median cleft lip repair. At 6 years of age, hypertelorism was corrected by wedge resection of the frontal and nasal bones and medial mobilization of the orbits. Follow-up was continued until 25 years of age, which revealed excellent maintenance of correction.
: Sphenoethmoidal encephalocele is a rare sporadic congenital cranial floor defect associated with typical facial and cerebral anomalies. Encephaloceles extending into the nasopharynx may cause airway obstruction and feeding difficulty and present a potential pathway for central nervous system infection. Repair of the encephalocele should then be performed as soon as possible. Care of patients with nasopharyngeal encephaloceles requires a lifetime of reconstructive surgery. Care of these patients can be rewarding to both families and surgeons.
脑膨出是指任何颅内物质通过颅骨缺损处向外延伸或突出。蝶筛部脑膨出通常是致命的。对于那些存活时间足够长的患者,迅速修复至关重要。我们报告了一例通过经颅和经腭联合入路成功修复的病例,由于修复成功,患者接受了多次二期重建,并进行了25年的随访。
一名体重3960克、足月顺产的男婴因臀位行剖宫产出生。初始检查发现一个2×3厘米的灰色口内鼻咽部肿物,黏膜覆盖光滑,经中线腭裂处突出。患儿4周大时,通过双额开颅术对脑膨出进行了硬膜外和硬膜内探查。15个月大时,患者接受了唇裂正中修复术。6岁时,通过楔形切除额骨和鼻骨以及眼眶内侧移位矫正了两眼间距过宽。随访持续至25岁,结果显示矫正效果维持良好。
蝶筛部脑膨出是一种罕见的散发性先天性颅底缺损,伴有典型的面部和脑部异常。延伸至鼻咽部的脑膨出可能导致气道阻塞和喂养困难,并为中枢神经系统感染提供潜在途径。因此,应尽快对脑膨出进行修复。鼻咽部脑膨出患者的护理需要终身进行重建手术。对这些患者的护理对家庭和外科医生来说都是有意义的。