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Frontoethmoidal Cephalocele: Our Experience of Eleven Cases Managed Surgically

机译:额筛窦性头颅囊肿:我们通过手术治疗的11例病例的经验

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Introduction: 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. Aim: To describe the particularity of the management of frontoethmoidal cephaloceles in our country. Methods: 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. Results: 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. Conclusion: 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. (C) 2015 S. Karger AG, Basel
机译:简介:额骨筛窦或窦性头突囊肿是先天性畸形,其特征是通过额骨和筛骨之间的先天性骨缺损使脑膜和/或脑组织外化。这些鼻窦头突很少见。虽然在发达国家,所采取的措施几乎使这种病理的发生频率为零,但在我们的工作环境中,这些措施实际上是不存在的,因此额筛窦性脑膨出仍然是我们关注的问题之一。目的:描述我国额筛窦头突的治疗的特殊性。方法:这是一项回顾性研究,于2007年1月1日至2013年6月30日进行。该研究涉及瓦加杜古大学医院神经外科治疗的所有额筛窦性脑膨出病例。结果:在6.5年内共治疗了11例患者(女性6例,男性5例)。患者年龄在1天至12岁之间,其中8例(72.72%)小于4个月大。产前超声诊断出1例。临床上,所有病例均由先天性头颅肿胀逐渐增加组成。所有病例均进行CT扫描,其中2例行相关肿块超声检查。对所有3例患者进行了经颅入路,并切开了肿块以减少多余的皮肤。 10例患者术后即刻病程良好。脑脊髓膜炎观察到1例死亡。我们注意到1例复发病例。结论:额筛窦头突的手术治疗很复杂,有时需要一个多学科团队。但是,在出现重要的骨畸形之前尽早关闭畸形可以阻止颌面部手术。就重要的预后而言,手术结果令人满意。但是,由于担心长期或多或少会出现精神运动迟缓,以及早期手术的并发症,这使得预防的建议和重点成为我们的主要关注点。 (C)2015 S.Karger AG,巴塞尔

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