Goto Michiko, Ohnishi Yuichi, Shoju Yuichi, Wato Masahiro, Kakudo Kenji
Second Department of Oral and Maxillofacial Surgery, Osaka Dental University, Osaka, Osaka 540-0008, Japan.
Department of Oral Pathology, Osaka Dental University, Osaka, Osaka 540-0008, Japan.
Oncol Lett. 2016 Feb;11(2):1220-1222. doi: 10.3892/ol.2015.3978. Epub 2015 Nov 30.
Papillary cystadenomas of the salivary gland are uncommon, benign, encapsulated or well-circumscribed, multicystic tumors with intracystic papillations. In a large review, papillary cystadenoma constituted 2% of all minor salivary gland tumors. The present study reports an extremely rare case of a papillary cystadenoma arising from the palate that demonstrated oncocytic features. A 60-year-old man was referred by his dentist to the Second Department of Oral and Maxillofacial Surgery at Osaka Dental University Hospital for the diagnostic evaluation of a mass of the left palate. An incisional biopsy was performed and the microscopic findings were interpreted as consistent with a papillary oncocytic cystadenoma. Therefore, the lesion was excised under general anesthesia. The post-operative course was uneventful and no recurrence had developed 5 years subsequent to surgery.
涎腺乳头状囊腺瘤并不常见,是一种良性、有包膜或边界清楚的多房性肿瘤,囊内有乳头状突起。在一项大型综述中,乳头状囊腺瘤占所有小涎腺肿瘤的2%。本研究报告了1例极为罕见的起源于腭部且具有嗜酸性细胞特征的乳头状囊腺瘤病例。一名60岁男性被其牙医转诊至大阪牙科大学医院口腔颌面外科第二科室,以对左侧腭部肿物进行诊断评估。进行了切开活检,显微镜检查结果显示与乳头状嗜酸性细胞囊腺瘤相符。因此,在全身麻醉下切除了病变。术后过程顺利,术后5年未出现复发。