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Posterior Fossa Decompression Combined with Resection of the Cerebellomedullary Fissure Membrane and Expansile Duraplasty: A Radical and Rational Surgical Treatment for Arnold–Chiari Type I Malformation

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Abstract

This study aims to introduce a new surgical procedure for the treatment of Arnold–Chiari type I malformation (ACM-1) and to compare its effectiveness with the techniques described in previous studies. We performed the following procedures: foramen magnum decompression combined with the removal of both the atlanto-occipital membrane, extended resection of the cerebellomedullary fissure arachnoid membrane, and artificial duraplasty to enlarge the membranic posterior fossa without resecting the cerebellar tonsils and syringosubarachnoid shunting. There were 21 ACM-1 patients: 12 cases had osteo-compression on the cerebellar hemisphere, 18 cases had thickened adhered fabric ring that stretched from arachnoid membrane to cerebellar hemisphere, and 15 cases with syringomyelia. The patients were followed up for 6 months to 3 years after the surgery. All patients showed a remarkable recovery of syringomyelia. There were no morbidity or death related to the surgery. Most of ACM-1 patients, the osteo- and membrane compression on cerebellar hemisphere and tonsil were observed during the operation. Therefore, decompression of foramen magnum and posterior craniocervical combined with the removal of cerebellomedullary fissure arachnoid membrane and placement of an artificial dural graft should be considered as a comprehensive option of minimally invasive surgery and rational and radical treatment of ACM-1. Our experience showed that, by using our procedure, shunting becomes no longer necessary in the treatment of ACM-1-associated syringomyelia.

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Correspondence to Chen Jian Liang or Huang Xiao Ping.

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Liang, C.J., Dong, Q.J., Xing, Y.H. et al. Posterior Fossa Decompression Combined with Resection of the Cerebellomedullary Fissure Membrane and Expansile Duraplasty: A Radical and Rational Surgical Treatment for Arnold–Chiari Type I Malformation. Cell Biochem Biophys 70, 1817–1821 (2014). https://doi.org/10.1007/s12013-014-0135-x

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  • DOI: https://doi.org/10.1007/s12013-014-0135-x

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