首页> 外文期刊>Journal of Surgical Case Reports >Middle ear choristoma presenting as cholesteatoma with conductive hearing loss
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Middle ear choristoma presenting as cholesteatoma with conductive hearing loss

机译:中耳胆脂瘤表现为胆脂瘤并伴有传导性听力损失

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A 6-year-old male was seen for evaluation of middle ear polyp with associated hearing loss and otorrhea. CT scan revealed canal polyp with a stalk extending to the middle ear with malformation of the malleus and incus. The patient underwent exploratory tympanotomy which revealed a fistula from the bony-cartilaginous junction connecting to a middle ear mass which had eroded the incus. Intraoperative pathology suggested columnar epithelium without cholesteatoma or muscle. Final pathologic diagnosis reported dense fibrous tissue as well as ectopic salivary gland tissue, consistent with salivary gland choristoma. After removal of the mass, a partial prosthesis was successfully placed. Middle ear salivary gland choristoma is a rare entity. It can be confused clinically with cholesteatoma and is usually diagnosed on pathology. This diagnosis is often associated with other external, middle, and inner ear abnormalities.
机译:观察到一名6岁男性用于评估中耳息肉并伴有听力损失和耳漏。 CT扫描显示管息肉,柄延伸至中耳,并有锤骨和砧骨畸形。该患者进行了探索性鼓室切开术,发现该鼓膜的骨-软骨连接处有瘘管,该瘘管已侵蚀了中耳。术中病理提示柱状上皮无胆脂瘤或肌肉。最终病理诊断报告为致密的纤维组织以及异位唾液腺组织,与唾液腺胆管瘤一致。去除肿块后,成功放置了部分假体。中耳涎腺胆管瘤是一种罕见的实体。临床上可将其与胆脂瘤混淆,通常可在病理学上诊断出来。该诊断通常与其他外耳,中耳和内耳异常相关。

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