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额筛窦脑膨出合并室管膜下结节性异位:一种不寻常的关联。病例报告。

Frontoethmoidal encephalocele with subependymal nodular heterotopia: an unusual association. A case report.

作者信息

Balaji R, Mangaleswaran B, John R

机构信息

Department of Radiology, Apollo Specialty Hospital Chennai; Trivandrum, India -

出版信息

Neuroradiol J. 2010 Jun;23(3):317-20. doi: 10.1177/197140091002300310. Epub 2010 Jun 30.

Abstract

Frontonasal encephaloceles involve herniation of meninges and brain tissue through defects in the floor of the anterior cranial fossa affecting the frontal, ethmoid and nasal bones. Subependymal nodular heterotopias are malformations of cortical development resulting from abnormal neuronal migration. This report describes the coexistence and association of these two entities which is extremely rare. We describe an unusual case of a six-year-old girl with a frontonasal encephalocele in whom further imaging disclosed subependymal nodular heterotopias. Clinically she presented with swelling over the glabella since birth but otherwise was asymptomatic. CT and MRI showed herniation of brain tissue with the overlying dura and CSF through a defect in the frontal, ethmoid and nasal bones. In addition, MRI revealed heterotopic nodules in the subependymal regions of the lateral ventricles that were isointense with grey matter on all sequences. The patient underwent one stage surgery for correction of the encephalocele.

摘要

额鼻脑膨出是指脑膜和脑组织通过颅前窝底部的缺损疝出,累及额骨、筛骨和鼻骨。室管膜下结节性异位是由于神经元迁移异常导致的皮质发育畸形。本报告描述了这两种极为罕见的病变同时存在并相关联的情况。我们报道了一例不寻常的6岁女孩,患有额鼻脑膨出,进一步影像学检查发现其存在室管膜下结节性异位。临床上,她自出生以来眉间就有肿胀,但无其他症状。CT和MRI显示脑组织连同上方的硬脑膜和脑脊液通过额骨、筛骨和鼻骨的缺损疝出。此外,MRI显示侧脑室室管膜下区域有异位结节,在所有序列上与灰质信号强度相等。该患者接受了一期手术矫正脑膨出。

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