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听觉失认症作为儿童肾上腺脑白质营养不良的一种临床症状。

Auditory agnosia as a clinical symptom of childhood adrenoleukodystrophy.

作者信息

Furushima Wakana, Kaga Makiko, Nakamura Masako, Gunji Atsuko, Inagaki Masumi

机构信息

Department of Developmental Disorders, National Institute of Mental Health, National Center of Neurology and Psychiatry, Japan; Department of Pediatrics, Tokyo Medical and Dental University, Japan.

Department of Developmental Disorders, National Institute of Mental Health, National Center of Neurology and Psychiatry, Japan; Department of Child Neurology, Tokyo Metropolitan Tobu Medical Center for Children/Adults with Developmental Disabilities, Japan.

出版信息

Brain Dev. 2015 Aug;37(7):690-7. doi: 10.1016/j.braindev.2014.10.011. Epub 2014 Dec 26.

Abstract

OBJECTIVE

To investigate detailed auditory features in patients with auditory impairment as the first clinical symptoms of childhood adrenoleukodystrophy (CSALD).

SUBJECTS AND METHODS

Three patients who had hearing difficulty as the first clinical signs and/or symptoms of ALD. Precise examination of the clinical characteristics of hearing and auditory function was performed, including assessments of pure tone audiometry, verbal sound discrimination, otoacoustic emission (OAE), and auditory brainstem response (ABR), as well as an environmental sound discrimination test, a sound lateralization test, and a dichotic listening test (DLT). The auditory pathway was evaluated by MRI in each patient.

RESULTS

Poor response to calling was detected in all patients. Two patients were not aware of their hearing difficulty, and had been diagnosed with normal hearing by otolaryngologists at first. Pure-tone audiometry disclosed normal hearing in all patients. All patients showed a normal wave V ABR threshold. Three patients showed obvious difficulty in discriminating verbal sounds, environmental sounds, and sound lateralization and strong left-ear suppression in a dichotic listening test. However, once they discriminated verbal sounds, they correctly understood the meaning. Two patients showed elongation of the I-V and III-V interwave intervals in ABR, but one showed no abnormality. MRIs of these three patients revealed signal changes in auditory radiation including in other subcortical areas.

CONCLUSION

The hearing features of these subjects were diagnosed as auditory agnosia and not aphasia. It should be emphasized that when patients are suspected to have hearing impairment but have no abnormalities in pure tone audiometry and/or ABR, this should not be diagnosed immediately as psychogenic response or pathomimesis, but auditory agnosia must also be considered.

摘要

目的

研究以听力障碍为儿童肾上腺脑白质营养不良(CSALD)首发临床症状的患者的详细听觉特征。

对象与方法

3例以听力困难为肾上腺脑白质营养不良(ALD)首发临床体征和/或症状的患者。对听力和听觉功能的临床特征进行了精确检查,包括纯音听力测定、言语声音辨别、耳声发射(OAE)和听觉脑干反应(ABR)评估,以及环境声音辨别测试、声音定位测试和双耳分听测试(DLT)。对每位患者进行MRI评估听觉通路。

结果

所有患者均被检测出对呼唤反应不佳。2例患者未意识到自己的听力困难,最初耳鼻喉科医生诊断其听力正常。纯音听力测定显示所有患者听力正常。所有患者的ABR波V阈值均正常。3例患者在言语声音、环境声音辨别和声音定位方面表现出明显困难,在双耳分听测试中左耳抑制明显。然而,一旦他们辨别出言语声音,就能正确理解其含义。2例患者的ABR中I-V和III-V波间期延长,但1例无异常。这3例患者的MRI显示听觉辐射包括其他皮质下区域有信号改变。

结论

这些受试者的听力特征被诊断为听觉失认而非失语。应强调的是,当怀疑患者有听力障碍但纯音听力测定和/或ABR无异常时,不应立即诊断为心理性反应或模仿症,还必须考虑听觉失认。

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