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骶骨发育不全与尾段脊髓畸形

Sacral agenesis and caudal spinal cord malformations.

作者信息

Pang D

机构信息

Department of Neurosurgery, Children's Hospital of Pittsburgh, Pennsylvania.

出版信息

Neurosurgery. 1993 May;32(5):755-78; discussion 778-9. doi: 10.1227/00006123-199305000-00009.

Abstract

Thirty-three children and one adult with sacral agenesis (SA) were studied by computed tomographic myelography and/or magnetic resonance imaging and were monitored for a mean period of 4.7 years. Four children had the OEIS (concurrent omphalocele, cloacal exstrophy, imperforate anus, and spinal deformities) complex, and three others had VATER (vertebral abnormality, anal imperforation, tracheoesophageal fistula, and renal-radial anomalies) syndrome. All patients shared some of the characteristic features of SA, namely, a short, intergluteal cleft, flattened buttocks, narrow hips, distal leg atrophy, and talipes deformities. Neurologically, lumbosacral sensation was much better preserved than the motor functions, and urinary and bowel symptoms were universal. The level of the vertebral aplasia was correlated with the motor but not with the sensory level. The important neuroimaging findings of SA were as follows: 1) 12 patients (35%) had nonstenotic, tapered narrowing of the caudal bony canal, and 2 patients had hyperostosis indenting the caudal thecal sac; 2) 16 patients (47%) had nonstenotic, tapered narrowing and shortening of the dural sac, but 3 patients (9%) had true, symptomatic dural stenosis, in which the cauda equina was severely constricted by a pencil-sized caudal dural sac; 3) the coni could be divided into those ending above the L1 vertebral body (Group 1, 14 patients) and those ending below L1 (Group 2, 20 patients). Thirteen of 14 Group 1 coni were club or wedge-shaped, terminating abruptly at T11 or T12, as if the normal tip was missing. All 20 Group 2 coni were tethered: 13 were tethered by a thick filum; 2 were extremely elongated and had a terminal hydromyelia; 3 were terminal myelocystoceles; and 2 were tethered by a transitional lipoma. High blunt coni were highly correlated with high (severe) sacral malformations (sacrum ending at S1), but low-lying tethered coni were highly correlated with low sacral malformations (S2 or lower pieces present).(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

对33名儿童和1名患有骶骨发育不全(SA)的成人进行了计算机断层脊髓造影和/或磁共振成像研究,并对他们进行了平均4.7年的监测。4名儿童患有OEIS(脐膨出、泄殖腔外翻、肛门闭锁和脊柱畸形并发)综合征,另外3名患有VATER(椎体异常、肛门闭锁、气管食管瘘和肾桡骨异常)综合征。所有患者都具有SA的一些特征,即臀间裂短、臀部扁平、臀部狭窄、小腿远端萎缩和足畸形。在神经方面,腰骶部感觉的保留情况比运动功能好得多,且泌尿和肠道症状普遍存在。椎体发育不全的水平与运动水平相关,但与感觉水平无关。SA的重要神经影像学表现如下:1)12例患者(35%)尾侧骨性椎管有非狭窄性、逐渐变细的狭窄,2例患者有骨质增生压迫尾侧硬脊膜囊;2)16例患者(47%)硬脊膜囊有非狭窄性、逐渐变细的狭窄和缩短,但3例患者(9%)有真正的、有症状的硬脊膜狭窄,其中马尾神经被铅笔粗细的尾侧硬脊膜囊严重压迫;3)圆锥可分为终止于L1椎体上方的(第1组,14例患者)和终止于L1下方的(第2组,20例患者)。第1组的14个圆锥中有13个呈棒状或楔形,在T11或T12处突然终止,就好像正常的尖端缺失了一样。第2组的所有20个圆锥都有脊髓栓系:13个被粗大的终丝栓系;2个极度拉长并伴有终末脊髓空洞症;3个是终末脊髓脊膜膨出;2个被过渡性脂肪瘤栓系。高位钝圆锥与高位(严重)骶骨畸形(骶骨止于S1)高度相关,但低位脊髓栓系圆锥与低位骶骨畸形(存在S2或更低节段)高度相关。(摘要截断于400字)

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