A Case of Primary EAC Cholesteatoma Extending into Antrum with Normal Middle Ear

S. Shrivastava, Rishita Kalra, Somyagupta Somyagupta, V. Pathak, P. Nayak, Stuti Shukla
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Abstract

Abstract Introduction  A cholesteatoma is a three-dimensional sac lined by keratinized squamous epithelium containing desquamated keratinized epithelial cell which secretes enzymes that have the tendency to expand and erode the bony structure underlying it and cause intracranial and extracranial complications. This cystic mass is in an abnormal location such as the middle ear, the petrous apex, or the external auditory canal (EAC). It is mostly found in the middle ear and rarely in the EAC. Here we have reported a rare case of unilateral primary EAC cholesteatoma with mild hearing loss in a middle-aged male. Case Report  We have reported a case of a 34-year-old male with complaints of right-sided ear discharge and right-sided decreased hearing for the last 5 to 6 years. On examination, right ear EAC was found to be dry, and a sac was observed in posterior wall extending to mastoid present with clear attic, and intact retracted tympanic membrane that was then followed by radiological evaluation to establish the diagnosis of EAC cholesteatoma. This was surgically treated and ear was cleared of all disease. Patient's symptoms improved postoperatively. Conclusion  Primary EAC cholesteatoma with disease-free middle ear is a rare finding and there is very less definitive literature available on the pathogenesis of the same.
原发性EAC胆脂瘤延伸至正常中耳鼻窦1例
胆脂瘤是一种由角质化的鳞状上皮内衬的三维囊,其中含有脱皮的角质化上皮细胞,其分泌的酶具有扩张和侵蚀其底层骨结构的倾向,并引起颅内和颅外并发症。囊性肿块位于异常位置,如中耳、岩尖或外耳道。它主要发生在中耳,很少发生在EAC。我们在此报告一例罕见的单侧原发性EAC胆脂瘤合并轻度听力损失的中年男性病例。病例报告我们报告了一例34岁男性,在过去的5至6年里,他的主诉是右耳分泌物和右侧听力下降。检查发现右耳EAC干燥,后壁可见囊囊延伸至乳突,有清晰的上盖,鼓膜完整缩回,影像学检查确定EAC胆脂瘤的诊断。手术治疗后,所有的疾病都被清除了。患者术后症状好转。结论原发性EAC胆脂瘤合并无病中耳是一种罕见的发现,其发病机制的明确文献很少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
11 weeks
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