Ukachukwu Aek, Shokunbi M T, Tiamiyu L O, Adeolu A A, Malomo A O
Department of Neurological Surgery, University College Hospital, Ibadan, Nigeria.
Department of Surgery, College of Medicine, University of Ibadan, Ibadan, Nigeria. Department of Neurological Surgery, University College Hospital, Ibadan, Nigeria.
J West Afr Coll Surg. 2018 Apr-Jun;8(2):76-90.
Syringomyelia is an often progressive disorder of the spinal cord. There is a dearth of reports in the African population.
This study describes the profile and the outcome of treatment in our population of patients.
A retrospective review of patients surgically treated for syringomyelia over a ten year period.
Department of Neurological Surgery, University College Hospital, Ibadan, Nigeria.
Eight patients were surgically treated for Syringomyelia over the period 2004-2014. We extracted data on their gender, age, aetiology, syrinx location, diagnosis, operative procedure and outcome. Simple statistical analysis was done.
There were five males and three females. The mean age was 31.6(SD15.3) years (median: 32.5 years). The causes of the syrinx were: Chiari malformation (3), intramedullary spinal tumour (2), foramen magnum tumour (1), post-traumatic (1), and iatrogenic chemical arachnoiditis (1). The syrinx location was: cervical region (4), cervicothoracic region (2) and multi-level (2). The operative procedures were posterior fossa decompression (2), sub-occipital craniectomy with laminectomy and tumour excision (2), laminectomy and syringomyelotomy (2), laminectomy and tumour excision (1), and ventriculoperitoneal shunting (1). The duration of follow up was 2 weeks to 35 months. Outcome was satisfactory in six patients. A child who had initial ventriculoperitoneal shunting died at home before definitive surgery, and an adult male died of respiratory insufficiency post operatively.
Syringomyelia is rare in our population. It affects young patients, typically in the cervico-thoracic region. The aetiologies are similar to those from previous reports. The outcome of surgical treatment in our small group of patients is satisfactory.
脊髓空洞症是一种常呈进行性发展的脊髓疾病。非洲人群中关于该病的报道较少。
本研究描述了我们所治疗患者群体的概况及治疗结果。
对10年间接受脊髓空洞症手术治疗的患者进行回顾性研究。
尼日利亚伊巴丹大学学院医院神经外科。
2004年至2014年期间,8例患者接受了脊髓空洞症手术治疗。我们提取了他们的性别、年龄、病因、空洞位置、诊断、手术方式及治疗结果等数据,并进行了简单的统计学分析。
男性5例,女性3例。平均年龄为31.6(标准差15.3)岁(中位数:32.5岁)。空洞形成的原因有:Chiari畸形(3例)、髓内脊髓肿瘤(2例)、枕骨大孔肿瘤(1例)、创伤后(1例)和医源性化学性蛛网膜炎(1例)。空洞位置为:颈部(4例)、颈胸段(2例)和多节段(2例)。手术方式包括后颅窝减压术(2例)、枕下颅骨切除术联合椎板切除术及肿瘤切除术(2例)、椎板切除术及脊髓空洞切开术(2例)、椎板切除术及肿瘤切除术(1例)和脑室腹腔分流术(1例)。随访时间为2周至35个月。6例患者的治疗结果满意。1例最初接受脑室腹腔分流术的儿童在确定性手术前在家中死亡,1例成年男性术后死于呼吸功能不全。
脊髓空洞症在我们的患者群体中较为罕见。它影响年轻患者,典型部位为颈胸段。病因与既往报道相似。我们这一小群患者的手术治疗结果令人满意。