Cochrane D D, Finley C, Kestle J, Steinbok P
Division of Pediatric Neurosurgery, Children's and Women's Health Center of British Columbia, Vancouver, Canada.
Eur J Pediatr Surg. 2000 Dec;10 Suppl 1:13-7. doi: 10.1055/s-2008-1072406.
Tethering is assumed to be the primary cause of deterioration seen in children with transitional lipomyelomeningocele as they age. The inevitability of deterioration has led to recommendations for prophylactic interventions to stabilize or prevent further clinical deterioration.
Determine the frequency and patterns of functional deterioration observed after successful untethering in patients with transitional lipomyelomeningocele and compare functional outcomes with what is known regarding untreated patients.
Fifty patients having transitional LMMC, treated at a single institution and followed in a multidisciplinary clinic were retrospectively reviewed to determine their clinical status prior to untethering, and the time to development of new symptoms or signs following untethering.
82% of patients were diagnosed and 78% underwent untethering prior to one year of age. All patients had a cutaneous lumbosacral lipoma, 22 patients were considered normal at presentation and 28 showed abnormalities on clinical examination. Forty-nine patients were untethered successfully and all were available for follow-up ranging from 2 to 138 months (mean 39 months). Acute morbidity was limited to transient neurogenic bladder dysfunction and minor wound complications. Late clinical deterioration occurred in the majority of patients. Orthopedic and neurological deterioration occurred over the first 60 months following untethering and urological deterioration occurred thereafter.
Functional loss after untethering is common and the pattern of loss is likely a reflection of the ability to detect abnormalities in this infant population. Untethering does not usually result in permanent acute morbidity, and does not prevent longer-term functional deterioration. The ratio of asymptomatic to symptomatic patients at follow-up in this operative series is similar to age-matched historical series of untreated patients.
随着年龄增长,脊髓栓系被认为是导致脊髓脊膜膨出合并脂肪瘤型脊髓脊膜膨出患儿病情恶化的主要原因。病情恶化的不可避免性促使人们建议采取预防性干预措施来稳定病情或防止进一步的临床恶化。
确定脊髓脊膜膨出合并脂肪瘤型脊髓脊膜膨出患者成功松解栓系后功能恶化的频率和模式,并将功能结果与未治疗患者的已知情况进行比较。
回顾性分析在单一机构接受治疗并在多学科诊所随访的50例脊髓脊膜膨出合并脂肪瘤型脊髓脊膜膨出患者,以确定其松解栓系前的临床状况以及松解栓系后出现新症状或体征的时间。
82%的患者在1岁前被诊断出,78%的患者在1岁前接受了栓系松解术。所有患者均有腰骶部皮肤脂肪瘤,22例患者初诊时被认为正常,28例患者临床检查有异常。49例患者成功松解栓系,所有患者均接受了随访,随访时间为2至138个月(平均39个月)。急性发病率仅限于短暂性神经源性膀胱功能障碍和轻微伤口并发症。大多数患者出现了晚期临床恶化。矫形和神经功能恶化发生在松解栓系后的前60个月,泌尿系统恶化在此之后发生。
松解栓系后功能丧失很常见,丧失模式可能反映了在这一婴儿群体中检测异常的能力。松解栓系通常不会导致永久性急性发病率,也不能防止长期功能恶化。该手术系列随访中无症状与有症状患者的比例与年龄匹配的未治疗患者历史系列相似。