Yamasoba T, Harada T, Okuno T, Nomura Y
Department of Otolaryngology, University of Tokyo, Japan.
Arch Otolaryngol Head Neck Surg. 1990 Oct;116(10):1214-6. doi: 10.1001/archotol.1990.01870100108025.
Osteomas of the middle ear are rare. We report a case of a 7-year-old boy with osteoma originating from the pyramidal eminence, combined with congenital cholesteatoma. The osteoma and cholesteatoma were successfully removed by tympanomastoidectomy. The long process of the incus and the superstructure of the stapes disappeared. The body of the incus was sculpted and used as a columella. Histopathologically, the osteoma was much the same as an external auditory canal osteoma. The possibility of a primary congenital origin of this neoplasm is suggested.
中耳骨瘤较为罕见。我们报告一例7岁男孩,其骨瘤起源于锥隆起,合并先天性胆脂瘤。通过鼓室乳突切除术成功切除了骨瘤和胆脂瘤。砧骨长突和镫骨上部结构消失。将砧骨体塑形后用作小柱。组织病理学检查显示,该骨瘤与外耳道骨瘤极为相似。提示该肿瘤可能为原发性先天性起源。