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Spontaneous regression of a terminal myelocystocele and associated syringomyelia: a case report.

作者信息

Durnford Andrew J, Mulik Roopa, Kay Andrew D

机构信息

School of Medicine, Birmingham University, Vincent Drive, Birmingham, B15 2TT, UK.

出版信息

Childs Nerv Syst. 2010 Mar;26(3):403-6. doi: 10.1007/s00381-009-1065-6.

DOI:10.1007/s00381-009-1065-6
PMID:20183927
Abstract

INTRODUCTION

Terminal myelocystocele is a rare form of spinal dysraphism characterised by cystic dilatation of the central canal of a low-lying terminal cord. Typical presentation is a skin-covered dorsal mass; early surgical repair has been recommended.

CASE REPORT

We present the case of a 4-year-old girl with a terminal myelocystocele and syrinx, which were both observed to spontaneously regress on subsequent magnetic resonance imaging.

CONCLUSION

Terminal myelocystocele and its associated syrinx may resolve spontaneously. Early surgical repair may not always be necessary.

摘要

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本文引用的文献

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Terminal and nonterminal myelocystoceles.终末型和非终末型脊髓脊膜膨出。
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Spontaneous regression of lipomyelomeningocele associated with terminal syringomyelia in a child. Case report.儿童终丝空洞症合并脂肪脊髓脊膜膨出的自然消退。病例报告。
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Terminal myelocystocele.
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