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一名11岁男孩患有Chiari I型畸形、胼胝体发育不全及颅咽管开放。

Chiari type 1 malformation, corpus callosum agenesis and patent craniopharyngeal canal in an 11-year-old boy.

作者信息

Tijssen Maud Pm, Poretti Andrea, Huisman Thierry Agm

机构信息

Section of Pediatric Neuroradiology, Division of Pediatric Radiology, Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, USA Department of Radiology, Maastricht University Medical Center, The Netherlands

Section of Pediatric Neuroradiology, Division of Pediatric Radiology, Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, USA.

出版信息

Neuroradiol J. 2016 Oct;29(5):307-9. doi: 10.1177/1971400916656487. Epub 2016 Jun 21.

Abstract

We describe the neuroimaging findings of an 11-year-old boy who presented with mild occipital headache and precocious puberty. This child was found to have a combination of various midline anomalies including a Chiari type 1 malformation, corpus callosum agenesis and patent craniopharyngeal canal with adjacent intracranial dermoid cyst.

摘要

我们描述了一名11岁男孩的神经影像学检查结果,该男孩表现为轻度枕部头痛和性早熟。这名儿童被发现存在多种中线异常的组合,包括Chiari I型畸形、胼胝体发育不全以及颅咽管开放伴相邻颅内皮样囊肿。

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