Tokashiki Kunihiko, Tsukahara Kiyoaki, Motohashi Ray, Nakamura Kazuhiro, Suzuki Mamoru
Otorhinolaryngology, Head & Neck Surgery, Tokyo Medical University Hachioji Medical Center, 403 La Conte Shinjuku, Nishi-Shinjuku 5-8-6, Shinjuku-ku, Tokyo 160-0023, Japan.
Case Rep Otolaryngol. 2013;2013:384238. doi: 10.1155/2013/384238. Epub 2013 Sep 12.
Primary submandibular gland oncocytic carcinoma is a rare pathology, with only 10 cases being reported to date. We encountered a case of primary submandibular gland oncocytic carcinoma and report it herein. The patient was a 69-year-old man who came to our hospital with right submandibular cancer as the main complaint. Based on the results of computed tomography and magnetic resonance imaging, submandibular gland tumor was diagnosed. Preoperative cytodiagnosis suggested class III oncocytic carcinoma. Resection of the right submandibular tumor was performed along with right neck dissection. Postoperative histopathological diagnosis was oncocytic carcinoma. As of 3 years following surgery, no recurrence has been identified.
原发性下颌下腺嗜酸性细胞癌是一种罕见的病理类型,迄今为止仅有10例报道。我们遇到一例原发性下颌下腺嗜酸性细胞癌,并在此报告。患者为69岁男性,以右下颌下癌为主诉前来我院就诊。根据计算机断层扫描和磁共振成像结果,诊断为下颌下腺肿瘤。术前细胞诊断提示为III级嗜酸性细胞癌。行右下颌下肿瘤切除及右颈清扫术。术后组织病理学诊断为嗜酸性细胞癌。截至手术3年后,未发现复发。