Colak A, Pollack I F, Albright A L
Department of Neurosurgery,Children's Hospital of Pittsburgh, University of Pittsburgh School ofMedicine, Pittsburgh, Pa., USA.
Pediatr Neurosurg. 1998 Oct;29(4):184-90. doi: 10.1159/000028719.
The authors reviewed the records of 94 patients who underwent initial repair of a lipomyelomeningocele between 1982 and July 1996 at the Children's Hospital of Pittsburgh to determine the incidence and time course of symptomatic retethering. In each of these patients, the initial operative goals were to microsurgically debulk as much of the lipoma as possible to allow the conus to move freely within the spinal canal, to divide any tethering arachnoidal adhesions, to close the pia if possible and to reconstitute a capacious thecal sac, using a dural graft if necessary. With a median follow-up of 58 months, 19 of these patients (20.2%) required 28 subsequent operations for symptomatic retethering. Median time between the initial procedure and reoperation for retethering was 52 months. The primary complaint of 12 patients was intractable low-back or leg pain. Other common symptoms were progressive bowel and/or bladder dysfunction, deterioration of motor function and foot deformities. The decision to reoperate was based predominantly on the clinical situation of the patient; magnetic resonance imaging was used to confirm the location and extent of tethering. Patients with transitional lipomas had a significantly higher frequency of symptomatic retethering than those with caudal or dorsal lesions (p < 0.05). No other clinical or technical feature correlated with an increased frequency of retethering. In particular, none of a variety of types of dural graft materials appeared to entirely prevent symptomatic retethering. Following reoperation, pain complaints resolved and many of the other symptoms improved partially or resolved completely. Although the long-term results were also favorable in the majority of patients, a small subgroup (n = 6) exhibited repetitive symptomatic tethering that proved increasingly difficult to treat. We concluded that symptomatic retethering is a common problem in children with lipomyelomeningoceles, even after an adequate initial operation. To date, no type of graft material has been shown to entirely prevent this problem. Close long-term surveillance of such patients is required to allow detection and treatment of symptomatic retethering.
作者回顾了1982年至1996年7月期间在匹兹堡儿童医院接受首次脂肪脊髓脊膜膨出修补术的94例患者的记录,以确定症状性脊髓栓系的发生率和病程。在这些患者中,每例患者最初的手术目标是通过显微手术尽可能多地切除脂肪瘤,以使圆锥在椎管内自由移动,分离任何脊髓蛛网膜粘连,如有可能缝合软膜,并重建一个宽敞的硬膜囊,必要时使用硬脑膜移植物。中位随访时间为58个月,其中19例患者(20.2%)因症状性脊髓栓系需要进行28次后续手术。首次手术与脊髓栓系再次手术之间的中位时间为52个月。12例患者的主要主诉是顽固性腰背痛或腿痛。其他常见症状包括进行性肠道和/或膀胱功能障碍、运动功能恶化和足部畸形。再次手术的决定主要基于患者的临床情况;磁共振成像用于确认脊髓栓系的位置和范围。过渡性脂肪瘤患者症状性脊髓栓系的发生率明显高于尾侧或背侧病变患者(p<0.05)。没有其他临床或技术特征与脊髓栓系发生率增加相关。特别是,各种类型的硬脑膜移植物材料似乎都不能完全预防症状性脊髓栓系。再次手术后,疼痛症状得到缓解,许多其他症状部分改善或完全缓解。虽然大多数患者的长期结果也很理想,但一小部分患者(n = 6)表现出反复的症状性脊髓栓系,且治疗难度越来越大。我们得出结论,症状性脊髓栓系在脂肪脊髓脊膜膨出患儿中是一个常见问题,即使在初次手术充分的情况下也是如此。迄今为止,没有一种移植物材料被证明能完全预防这个问题。需要对这些患者进行密切的长期监测,以便发现和治疗症状性脊髓栓系。