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腭部黏液表皮样癌:1例罕见病例报告

Mucoepidermoid carcinoma of the palate: A rare case report.

作者信息

Jarde Samiksha Jaypal, Das Sushma, Narayanswamy Savitha Arumugam, Chatterjee Anirban, Babu Chaitanya

机构信息

Department of Periodontics, The Oxford Dental College and Hospital, Bomanahalli, Bengaluru, Karnataka, India.

Department of Oral and Maxillofacial Pathology, The Oxford Dental College and Hospital, Bomanahalli, Bengaluru, Karnataka, India.

出版信息

J Indian Soc Periodontol. 2016 Mar-Apr;20(2):203-6. doi: 10.4103/0972-124X.170828.

Abstract

Mucoepidermoid carcinomas (MECs) of minor salivary gland origin are rare in children and adolescents and have been reported rarely. Literature regarding their clinical features and biologic behavior is scanty. The purpose of this case report is to discuss the clinical manifestation, diagnosis, and treatment plan of MEC of the palate. A 16-year-old male subject visited the Department of Periodontics, The Oxford Dental College and Hospital, Bangalore, India complaining of a painless swelling in the left posterior area of the hard palate since 6 months. Several clinical, radiographic, and histopathological investigations were carried out to rule out the lesion. Incisional biopsy of the lesion confirmed the diagnosis of lesion as MEC of the palate following which a wide surgical excision with adjacent free margins was carried out. This case report highlights the need for proper diagnosis and treatment plan in the cases of malignant tumors as it can lead to morbidity and mortality.

摘要

小唾液腺来源的黏液表皮样癌(MEC)在儿童和青少年中罕见,相关报道也很少。关于其临床特征和生物学行为的文献稀少。本病例报告的目的是探讨腭部MEC的临床表现、诊断和治疗方案。一名16岁男性患者前往印度班加罗尔牛津牙科学院及医院牙周病科就诊,主诉硬腭左侧后部无痛性肿胀已6个月。进行了多项临床、影像学和组织病理学检查以排除该病变。病变的切开活检确诊为腭部MEC,随后进行了广泛的手术切除并带有相邻的切缘。本病例报告强调了在恶性肿瘤病例中制定正确诊断和治疗方案的必要性,因为这可能导致发病和死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c04/4847470/e43c20c17c50/JISP-20-203-g001.jpg

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