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患有巨脑畸形的无脑白质囊性病的极重度聋儿的人工耳蜗植入

Cochlear implantation in a profoundly deaf child with cystic leukoencephalopathy without megalencephaly.

机构信息

Department of ENT, Jawaharlal Institute of Post Graduate Medical Education and Research, Pondicherry, India.

出版信息

J Laryngol Otol. 2023 May;137(5):584-587. doi: 10.1017/S0022215122001931. Epub 2022 Aug 18.

Abstract

BACKGROUND

Cochlear implantation candidacy criteria have continued to evolve over the years, and cochlear implantation is possible with many inner-ear and brain anomalies with good hearing and linguistic outcomes. Cystic leukoencephalopathy without megalencephaly is a rare disease in children, with only 30 cases reported in the literature, but it is associated with hearing loss in only three cases. Radiological investigations can help in diagnosing this rare entity before proceeding with cochlear implantation.

CASE REPORT

A four-year-old female child born out of consanguinity with normal psychomotor development, bilateral sensorineural hearing loss and an incidental magnetic resonance imaging finding of cystic leukoencephalopathy without megalencephaly underwent successful cochlear implantation. Her post-operative period was uneventful with successful mapping of the cochlear implant.

CONCLUSION

This is the first reported case of cystic leukoencephalopathy without megalencephaly and with sensorineural hearing loss in which cochlear implantation was performed successfully. White matter and temporal lobe abnormalities should not deter paediatric cochlear implantation.

摘要

背景

多年来,耳蜗植入的候选标准不断发展,许多内耳和脑部异常的患者也可以进行耳蜗植入,并且获得良好的听力和语言效果。无脑回巨脑畸形伴脑白质囊性病变是一种罕见的儿童疾病,文献中仅报告了 30 例,但仅有 3 例与听力损失相关。放射学检查有助于在进行耳蜗植入前诊断这种罕见疾病。

病例报告

一名 4 岁的女性儿童,出生于近亲结婚,精神运动发育正常,双侧感音神经性听力损失,偶然发现磁共振成像存在无脑回巨脑畸形伴脑白质囊性病变,成功接受了耳蜗植入。她的术后期间没有出现异常,耳蜗植入成功进行了映射。

结论

这是首例报道的无脑回巨脑畸形伴感音神经性听力损失且成功进行耳蜗植入的病例。白质和颞叶异常不应阻止儿童进行耳蜗植入。

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