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作 者:汪舟[1] 朱泽章[1] 邱勇[1] 蒋健[1] 钱邦平[1] 沙士甫[1] 谢丁丁[1] 江龙[1]
机构地区:[1]南京大学医学院附属鼓楼医院脊柱外科,210008
出 处:《中华小儿外科杂志》2014年第12期940-943,共4页Chinese Journal of Pediatric Surgery
基 金:国家自然科学基金面上项目(81171672)
摘 要:目的探讨青少年Chiari畸形伴脊髓空洞患儿后颅窝减压术(posterior fossa decompression,PFD)中施行空洞分流的必要性。方法回顾性分析2005年6月至2009年12月间我院后颅窝减压术治疗的40例青少年Chiari畸形伴脊髓空洞症患儿,根据术中是否施行脊髓空洞-蛛网膜下腔分流分为PFD+空洞分流组(A组)与单纯PFD组(B组)。其中,A组患儿18例,男6例,女12例,平均年龄13.5岁;B组患儿22例,男14例,女8例,平均年龄13.1岁。于T1加权MRI上测量术前及末次随访时空洞长度、最大脊髓空洞直径/脊髓直径值(S/C值),统计分析两组患儿的脊髓空洞改善程度是否存在差异。结果术前两组患儿性别、年龄、空洞大小均无显著差异。A组随访时间12-33个月,平均(16.8±6.1)个月;B组随访时间12-25个月,平均(16.4±3.3)个月。末次随访时,两组患儿空洞长度(9.0±6.5)个椎体、S/C值0.56±0.28均较其术前(13.1±4.5)个椎体和0.78±0.07显著减小,差异有统计学意义(P〈0.05)。A组平均空洞长度改善率、S/C值改善率分别为(34.4±37.5)%和(30.3±33.3)%;B组平均空洞长度改善率、S/C值改善率分别为(52.1±29.3)%和(41.2±31.2)%;组间比较差异没有统计学意义(P〉0.05)。A组空洞长度改善值为(4.1±5.1)节段,B组为(5.9±4.4)节段;A组S/C改善值为0.22土0.23,B组为0.32±0.26,组间差异均无统计学意义(P〉0.05)。结论空洞分流术对行后颅窝减压术的青少年Chiari畸形患儿的空洞转归无明显影响,然而其远期疗效有待更大样本、更长随访时间的研究行进一步证实。Objective To evaluate the necessity of syrinx shunting in adolescents undergoing posterior fossa decompression (PFD) for Chiari malformation and syringomyelia. Methods A total of 40 patients, aged 10 to 18 years, undergoing PFD for Chiari malformation between June 2005 and December 2009 were identified and retrospectively reviewed. They were classified into 2 groups based on whether or not shunting was performed., group A with PFD plus syrinx shunting (M: F = 6: 12; mean age, 13. 5 years) and group B with PFD alone (M:F= 14:8; mean age, 13. 1 years). On T1- weighted magnetic resonance imaging, syrinx length as well as maximal syrinx/cord (S/C) ratio was evaluated pre- and postoperatively. The extent of syrinx resolution was compared between two groups with Student's t test. Results During PFD, age, gender, syrinx length and S/C ratio did not differ significantly between two groups (P〉0. 05). The average follow-up periods of groups A and B were 16. 8 ± 6. 1(12-33)and 16. 4 ± 3. 3(12-25)months respectively. At the last follow-up, syrinx length and maximal S/C ratio decreased significantly in both groups (P〈0.05). The improvement rate of syrinx length and S/C ratio averaged 0. 34 ± 0. 37 and 0. 30 ± 0. 33 for Group A versus 0. 52 ± 0. 29 and 0.41 ± 0.31 for Group B respectively. No significant inter-group differences existed in the extent of improvement in syrinx length or S/C ratio (P〉0. 05). Conclusions In neurosurgical treatment of syringomyelia associated with Chiari malformation, syrinx shunting plus PFD shows no advantage over PFD alone in terms of decreasing syrinx length or S/C ratio.
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