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硬腭乳头状涎腺瘤:一例罕见病例报告。

Sialadenoma papilliferum of the hard palate: A rare case report.

作者信息

Atarbashi-Moghadam Saede, Lotfi Ali, Moshref Mohammad, Mokhtari Sepideh

机构信息

Department of Oral and Maxillofacial Pathology, School of Dentistry, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Indian J Pathol Microbiol. 2019 Jan-Mar;62(1):163-164. doi: 10.4103/IJPM.IJPM_687_17.

DOI:10.4103/IJPM.IJPM_687_17
PMID:30706887
Abstract

Sialadenoma papilliferum (SP) is a rare benign salivary gland tumor with unclear cell origin. This report presents a new case of SP of the hard palate occurring in a 50-year-old female. The lesion was completely excised, and the microscopic features were consistent with SP. The knowledge of this rare entity contributes to proper diagnosis and prevents unnecessary radical surgery and treatment.

摘要

乳头状唾液腺瘤(SP)是一种细胞起源不明的罕见良性唾液腺肿瘤。本报告介绍了一例发生在一名50岁女性硬腭的SP新病例。病变被完全切除,显微镜下特征与SP一致。了解这种罕见的实体有助于正确诊断,并避免不必要的根治性手术和治疗。

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引用本文的文献

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Oncocytic variant of sialadenoma papilliferum - a rare salivary gland tumor: A case report.乳头状唾液腺瘤的嗜酸性细胞变体——一种罕见的唾液腺肿瘤:病例报告
J Clin Exp Dent. 2022 Jul 1;14(7):e604-e607. doi: 10.4317/jced.59284. eCollection 2022 Jul.
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Sialadenoma papilliferum: clinicopathologic, Immunohistochemical, molecular analyses of new five cases and review of the literature.涎腺乳头囊腺瘤:五例新病例的临床病理、免疫组织化学和分子分析及文献复习。
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