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3个月大婴儿罕见的内耳道狭窄伴先天性面瘫病例报告

Rare Occurrence of Internal Auditory Canal Stenosis Accompanied With Congenital Facial Palsy in a 3-Month-Old Infant: A Case Report.

作者信息

Park Se-Heum, Kim Woo-Jin, Lim Yun-Jung, On Cheol-Won, Park Ji-Ho, Min Eun-Ho

机构信息

Department of Physical Medicine and Rehabilitation, Haeundae Paik Hospital, Inje University College of Medicine, Busan, Korea.

Department of Rehabilitation Medicine, Epworth HealthCare Epworth Richmond, Melbourne, Australia.

出版信息

Ann Rehabil Med. 2020 Jun;44(3):256-259. doi: 10.5535/arm.19148. Epub 2020 Jun 30.

DOI:10.5535/arm.19148
PMID:32640784
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7349044/
Abstract

Internal auditory canal (IAC) stenosis with hypoplasia of the facial and vestibulocochlear nerves is a rare cause of congenital facial palsy. In this case report, a 3-month-old female infant was referred for a neurological developmental assessment for developmental delay and congenital facial palsy. Upon evaluation of developmental delay, hearing loss was detected. Following a magnetic resonance imaging scan of the brain and a computed tomography scan of the temporal bone, IAC stenosis with hypoplasia of facial and vestibular nerves was diagnosed. This is a rare case of IAC stenosis in an infant with initial presentations of left facial palsy and developmental delay associated with hearing loss in the left ear. We strongly suggest that IAC stenosis be considered a cause of congenital facial palsy in infants, especially in patients with developmental delay. In infants with congenital facial palsy, a thorough physical examination and neurological developmental assessment should be performed.

摘要

内耳道(IAC)狭窄伴面神经和前庭蜗神经发育不全是先天性面瘫的罕见病因。在本病例报告中,一名3个月大的女婴因发育迟缓及先天性面瘫被转诊进行神经发育评估。在评估发育迟缓时,发现了听力损失。经脑部磁共振成像扫描和颞骨计算机断层扫描后,诊断为内耳道狭窄伴面神经和前庭神经发育不全。这是一例罕见的内耳道狭窄病例,患儿最初表现为左侧面瘫及发育迟缓,并伴有左耳听力损失。我们强烈建议将内耳道狭窄视为婴儿先天性面瘫的一个病因,尤其是在伴有发育迟缓的患者中。对于患有先天性面瘫的婴儿,应进行全面的体格检查和神经发育评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffef/7349044/db680162e42e/arm-19148f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffef/7349044/8edc6f88eed7/arm-19148f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffef/7349044/10391111cba1/arm-19148f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffef/7349044/045bf286fe50/arm-19148f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffef/7349044/db680162e42e/arm-19148f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffef/7349044/8edc6f88eed7/arm-19148f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffef/7349044/10391111cba1/arm-19148f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffef/7349044/045bf286fe50/arm-19148f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffef/7349044/db680162e42e/arm-19148f4.jpg

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