1型Chiari畸形伴寰椎同化减压术后7年C1再狭窄的微创外直视手术治疗。

Surgical neurology international Pub Date : 2025-07-18 eCollection Date: 2025-01-01 DOI:10.25259/SNI_480_2025
Yosuke Hashimoto, Hisaaki Uchikado, Yuko Baba, Takehiro Makizono, Jin Kikuchi, Motohiro Morioka
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引用次数: 0

摘要

背景:伴有寰椎同化(AA)的1型Chiari畸形(CM1)在无脊髓空洞的儿童中很少见。这里,一个13岁的孩子接受了原创性枕骨大孔减压术(FMD)治疗CM1。指数手术后7年,患者20岁,需要二次手术来解决CM1/AA引起的复发性C1狭窄,无需硬膜成形术。病例描述:一名13岁儿童,最初表现为头痛、CM1和AA,为此他接受了无硬脑膜成形术的FMD。7年后,20岁时,由于寰椎板背侧骨增生,患者复发性C1狭窄。在没有硬脑膜成形术的情况下,他进行了二次小开口外窥镜减压,无症状。结论:对于无脊髓空洞的CM1患者,反复小开口外显镜骨减压可成功治疗复发性狭窄。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mini-open exoscopic surgery for C1 restenosis 7 years after decompression of Chiari malformation type 1 with atlas assimilation.

Mini-open exoscopic surgery for C1 restenosis 7 years after decompression of Chiari malformation type 1 with atlas assimilation.

Mini-open exoscopic surgery for C1 restenosis 7 years after decompression of Chiari malformation type 1 with atlas assimilation.

Mini-open exoscopic surgery for C1 restenosis 7 years after decompression of Chiari malformation type 1 with atlas assimilation.

Background: Chiari malformation type 1 (CM1) associated with atlas assimilation (AA) is rarely encountered in children without syringomyelia. Here, a 13-year-old child underwent an original foramen magnum decompression (FMD) for a CM1. Seven years after the index surgery, at age 20, the patient required secondary surgery to address recurrent C1 stenosis attributed to CM1/AA performed without a duraplasty.

Case description: A 13-year-old child originally presented with headaches and CM1 and AA, for which he underwent a FMD without duraplasty. Seven years later, at the age of 20, he developed recurrent C1 stenosis attributed to dorsal bony proliferation of the lamina of the atlas. Following a secondary mini-open exoscopic decompression without duraplasty, he became asymptomatic.

Conclusion: For patients with CM1 without syringomyelia, recurrent stenosis may be successfully managed with repeated mini-open exoscopic bony decompression.

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