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中耳腺瘤1例罕见病例。

A rare case of middle ear adenoma.

作者信息

Baku Masayo, Ueda Hiromi

机构信息

Department of Otorhinolaryngology, Aichi Medical University, Nagakute, Japan.

出版信息

Nagoya J Med Sci. 2014 Aug;76(3-4):355-60.

Abstract

Middle ear adenoma is a rare disease that is thought to originate in the middle ear mucosa. It occurs over a wide age range, has no gender predilection, and is not characterized by specific symptoms or findings. The most frequent complaints are unilateral hearing loss and ear fullness. We report a 48-year-old woman with middle ear adenoma who had a history of unilateral ear fullness and hearing loss on the left side. Middle ear adenoma was suspected following a biopsy performed under local anesthesia. To remove the tumor, the patient underwent a left postauricular canal wall-up tympanoplasty type IIIc. Microscopic examination and immunohistochemistry confirmed a middle ear adenoma. In this case, we diagnosed the lesion as middle ear adenoma with neuroendocrine differentiation on the basis of the pathological findings. The patient has shown no recurrence for almost 5 years, but since this adenoma showed neuroendocrine differentiation, long-term observation is required.

摘要

中耳腺瘤是一种罕见疾病,被认为起源于中耳黏膜。它在广泛的年龄范围内发病,无性别倾向,也没有特定的症状或表现。最常见的主诉是单侧听力损失和耳闷。我们报告一例48岁患有中耳腺瘤的女性,她有左侧单侧耳闷和听力损失的病史。在局部麻醉下进行活检后怀疑为中耳腺瘤。为切除肿瘤,患者接受了左耳后IIIc型外耳道后壁上鼓室成形术。显微镜检查和免疫组化证实为中耳腺瘤。在本病例中,根据病理结果,我们将病变诊断为具有神经内分泌分化的中耳腺瘤。该患者近5年未复发,但由于此腺瘤显示神经内分泌分化,需要长期观察。

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