Zabsonre D Sylvain, Kabre Abel, Haro Yacouba
CHU Yalgado Ouedraogo, Ouagadougou, Burkina Faso.
Pediatr Neurosurg. 2015;50(1):7-11. doi: 10.1159/000369935. Epub 2015 Jan 13.
Frontoethmoidal or sincipital cephaloceles are congenital malformations characterized by externalization of the meninges and/or brain tissue through a congenital bone defect between the frontal and ethmoid bones. These sincipital cephaloceles are very infrequent. While in developed countries the measures taken have brought about virtually zero frequency of this pathology, in our work environment these measures are virtually nonexistent, so that frontoethmoidal cephaloceles remain one of our concerns.
To describe the particularity of the management of frontoethmoidal cephaloceles in our country.
This was a retrospective study carried out between January 1, 2007 and June 30, 2013. It concerned all cases of frontoethmoidal cephaloceles managed in the Neurosurgery Department of the University Hospital of Ouagadougou.
A total of 11 patients (6 females and 5 males) were attended to in 6.5 years. The age of the patients ranged from 1 day to 12 years, and 8 patients (72.72%) were less than 4 months old; 1 case was diagnosed at antenatal ultrasound. Clinically, all cases consisted of congenital cephalic swelling of gradual increase. A CT scan was performed in all cases and an ultrasound of the associated mass was carried out in 2 cases. Transcranial approach was done for all patients with 3 patients having had an incision of the mass to reduce redundant skin. The immediate postoperative course was favorable in 10 cases; 1 death was observed by cerebrospinal meningitis. We noted 1 case of recurrence.
The surgical treatment of frontoethmoidal cephaloceles is complex, sometimes requiring a multidisciplinary team. However, early closing of the malformation before the appearance of important bone deformities can prevent maxillofacial surgery. The results of the surgery are satisfactory as regards the vital prognosis. However, the fear of a more or less long-term occurrence of psychomotor retardation and the complications of early surgery make the recommendation and emphasis of prevention our main concern.
额筛部或头前部脑膨出是一种先天性畸形,其特征是脑膜和/或脑组织通过额骨和筛骨之间的先天性骨缺损向外突出。这些头前部脑膨出非常罕见。在发达国家,所采取的措施已使这种病理情况的发生率几乎为零,但在我们的工作环境中,这些措施几乎不存在,因此额筛部脑膨出仍然是我们关注的问题之一。
描述我国额筛部脑膨出治疗的特殊性。
这是一项在2007年1月1日至2013年6月30日期间进行的回顾性研究。该研究涉及在瓦加杜古大学医院神经外科治疗的所有额筛部脑膨出病例。
在6.5年的时间里共诊治了11例患者(6名女性和5名男性)。患者年龄从1天至12岁不等,8例患者(72.72%)年龄小于4个月;1例在产前超声检查时被诊断出来。临床上,所有病例均表现为先天性头部肿胀且逐渐增大。所有病例均进行了CT扫描,2例对相关肿块进行了超声检查。所有患者均采用经颅入路,3例患者对肿块进行了切开以减少多余皮肤。10例患者术后即刻病程良好;1例因脑脊液性脑膜炎死亡。我们注意到1例复发。
额筛部脑膨出的手术治疗很复杂,有时需要多学科团队参与。然而,在重要骨畸形出现之前尽早闭合畸形可避免颌面外科手术。就生命预后而言,手术结果令人满意。然而,对或多或少长期出现精神运动发育迟缓以及早期手术并发症的担忧使预防的建议和重点成为我们主要关注的问题。