中耳唾液腺瘤伴先天性单侧听力损失

IF 0.6 4区医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL

Acta medica Okayama Pub Date : 2024-08-01 DOI:10.18926/AMO/67554

Yuichiro Tominaga, Akiko Sugaya, Shin Kariya, Aiko Shimizu, Yuko Kataoka, Mizuo Ando

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引用次数: 0

摘要

中耳唾液腺瘤（SGCh）是一种罕见的良性肿瘤，由于中耳形态异常而导致传导性听力损失。早期诊断具有挑战性，手术切除是确诊的必要条件。我们报告了一例 3 岁男孩的病例，他在新生儿听力筛查（NHS）中发现左侧听力损失，在随访期间被诊断为中耳 SGCh。在新生儿听力筛查（NHS）结果出来后进行的长期随访、随后的计算机断层扫描/磁共振成像以及手术切除，使该病得到了相对较早的诊断和治疗。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Middle-Ear Salivary Gland Choristoma with Congenital, Single-Sided Hearing Loss.

Middle-ear salivary gland choristoma (SGCh) is a rare, benign tumor that causes conductive hearing loss owing to middle-ear morphological abnormalities. Early diagnosis is challenging, and surgical resection is indispensable for a definitive diagnosis. We report the case of a 3-year-old boy diagnosed with middle-ear SGCh during the follow-up period for left-sided hearing loss discovered at newborn hearing screening (NHS). Long-term follow-up after the NHS result, subsequent computed tomography/magnetic resonance imaging, and surgical resection led to its relatively early diagnosis and treatment.

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来源期刊

Acta medica Okayama 医学-医学：研究与实验

CiteScore

1.00

自引率

0.00%

发文量

110

审稿时长

6-12 weeks

期刊介绍： Acta Medica Okayama (AMO) publishes papers relating to all areas of basic and clinical medical science. Papers may be submitted by those not affiliated with Okayama University. Only original papers which have not been published or submitted elsewhere and timely review articles should be submitted. Original papers may be Full-length Articles or Short Communications. Case Reports are considered if they describe significant and substantial new findings. Preliminary observations are not accepted.