Adenoid cystic carcinoma in atypical site: case report

Amanda Rios Sampaio, Júlia Rusch Pinto Vasconcelos, Julyana Bastos Santana, Luis Filipe Alves Kian, D. O. Lopes
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Abstract

Adenoid cystic carcinoma (ACC) is a rare form of malignant neoplasm of the salivary glands, with slow growth and late symptoms. One of the challenges presented by this tumor is its high rate of metastasis, with tropism to the nervous system, liver and bones. Treatment is based on surgical resection of the tumor, radiotherapy, and chemotherapy – it varies depending on the condition of each patient. In view of the low frequency of ACC, this study aims to report a case of ACC in a female patient, with anatomopathological diagnosis of basaloid cell neoplasm.
非典型部位腺样囊性癌1例
腺样囊性癌(ACC)是一种罕见的涎腺恶性肿瘤,生长缓慢,症状较晚。这种肿瘤面临的挑战之一是它的高转移率,倾向于神经系统,肝脏和骨骼。治疗是基于手术切除肿瘤,放疗和化疗-它取决于每个病人的情况。鉴于ACC的发病率较低,本研究报告1例女性ACC患者,解剖病理诊断为基底细胞瘤。
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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