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脑桥被盖帽发育异常中的颞骨及颅神经表现

Temporal bone and cranial nerve findings in pontine tegmental cap dysplasia.

作者信息

Nixon Jason N, Dempsey Jennifer C, Doherty Dan, Ishak Gisele E

机构信息

M/S MA.7.220, Seattle Children's Hospital, PO Box 5371, Seattle, WA, 98145, USA.

Department of Radiology, University of Washington and Seattle Children's Hospital, Seattle, WA, USA.

出版信息

Neuroradiology. 2016 Feb;58(2):179-87. doi: 10.1007/s00234-015-1604-7. Epub 2015 Oct 12.

Abstract

INTRODUCTION

Pontine tegmental cap dysplasia (PTCD) is a recently described brain malformation associated with multiple cranial neuropathies, most commonly congenital sensorineural hearing loss. The purpose of this study is to systematically characterize the cranial nerve and temporal bone findings in a cohort of children with this rare condition.

METHODS

Sixteen patients with PTCD and diagnostic quality imaging were retrospectively reviewed. All patients had high-resolution MR of the brain and/or internal auditory canals, and seven patients had additional high-resolution CT of the temporal bones. Studies were evaluated by two pediatric neuroradiologists for cranial nerve and temporal bone anomalies.

RESULTS

Fifteen of 16 patients (94%) had duplication of one or both internal auditory canals. Of the 24 total duplicated internal auditory canals, all 24 (100%) demonstrated stenosis or atresia of the vestibulocochlear nerve canal, as well as ipsilateral vestibulocochlear nerve aplasia. Of the non-duplicated internal auditory canals, 63% (5/8) were atretic or stenotic. Thirty-eight percent (3/8) were associated with absent vestibulocochlear nerve, and 38% (3/8) demonstrated isolated cochlear nerve aplasia. Twenty-five percent (2/8) demonstrated normal vestibulocochlear nerves, both in the same patient. Fifteen of 16 patients overall (94%) demonstrated bilateral cochlear nerve aplasia. Of the 32 total temporal bones, 4 (13%) demonstrated facial nerve aplasia. Seventy-nine percent (22/28) of facial nerves that were present demonstrated an aberrant origin or course.

CONCLUSION

Patients with PTCD have highly characteristic temporal bone and cranial nerve findings on both CT and MR. Recognition of these findings is important for improved diagnosis of this rare disorder, particularly by CT.

摘要

引言

脑桥被盖部发育异常(PTCD)是一种最近描述的脑畸形,与多种颅神经病变相关,最常见的是先天性感音神经性听力损失。本研究的目的是系统地描述一组患有这种罕见疾病的儿童的颅神经和颞骨表现。

方法

对16例患有PTCD且有诊断质量影像资料的患者进行回顾性分析。所有患者均接受了脑部和/或内耳道的高分辨率磁共振成像(MR)检查,7例患者还接受了颞骨的高分辨率计算机断层扫描(CT)检查。由两名儿科神经放射科医生对研究进行评估,以确定颅神经和颞骨异常情况。

结果

16例患者中有15例(94%)存在一侧或双侧内耳道重复。在总共24条重复的内耳道中,所有24条(100%)均显示前庭蜗神经管狭窄或闭锁,以及同侧前庭蜗神经发育不全。在未重复的内耳道中,63%(5/8)闭锁或狭窄。38%(3/8)与前庭蜗神经缺如相关,38%(3/8)显示孤立的蜗神经发育不全。25%(2/8)在同一患者中显示前庭蜗神经正常。总体上,16例患者中有15例(94%)显示双侧蜗神经发育不全。在总共32块颞骨中,4块(13%)显示面神经发育不全。存在的面神经中有79%(22/28)显示起源或走行异常。

结论

PTCD患者在CT和MR上均有高度特征性的颞骨和颅神经表现。认识这些表现对于改善这种罕见疾病的诊断很重要,尤其是通过CT。

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