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扁桃体柱坏死性涎腺化生。1例罕见病例。

Necrotizing sialometaplasia of the tonsillar pillar. An unusual case.

作者信息

Hernández-Flores Julissa-Brillit, Santos-Jaimes Edmundo, Gaitán-Cepeda Luis-Alberto

机构信息

Second year resident of Oral pathology program, Graduate and Research Division, Dental School, National Autonomous University of Mexico. Mexico city, Mexico.

Professor of Department of Oral Pathology and Oral Medicine, Graduate and Research Division, Dental School, National Autonomous University of Mexico. Mexico city, Mexico.

出版信息

J Clin Exp Dent. 2021 Feb 1;13(2):e211-e214. doi: 10.4317/jced.57341. eCollection 2021 Feb.

DOI:10.4317/jced.57341
PMID:33575007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7864363/
Abstract

Necrotizing Sialometaplasia (NS) is a rare, benign, self-limited, inflammatory and necrotizing reaction of the salivary glandular tissue. Due to the clinical picture (a painful ulcer with well-defined edges), and histopathological characteristics (nuclear and cellular pleomorphism of ductal cells) NS can mimic a malignant lesion. The correct diagnosis is important because NS shows a spontaneous resolution and therefore no further treatment is needed. We report a very unusual case of spontaneous and recurrent NS located on the anterior tonsillar pillar in a 43-year old man, which clinically mimics a malignant lesion. The clinician should be aware to include NS in the differential diagnosis of ulcers in soft palate and tonsillar pillars. Minor salivary gland, necrotizing sialometaplasia, oral ulcer, squamous cell carcinoma, tonsillar pillar.

摘要

坏死性涎腺化生(NS)是一种罕见的、良性的、自限性的涎腺组织炎症性坏死反应。由于临床表现(边缘清晰的疼痛性溃疡)以及组织病理学特征(导管细胞核及细胞多形性),NS可酷似恶性病变。正确诊断很重要,因为NS可自行消退,因此无需进一步治疗。我们报告一例非常罕见的病例,一名43岁男性的扁桃体前柱出现自发性复发性NS,临床上酷似恶性病变。临床医生应注意将NS纳入软腭和扁桃体柱溃疡的鉴别诊断中。小涎腺、坏死性涎腺化生、口腔溃疡、鳞状细胞癌、扁桃体柱

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e87/7864363/6543a9083f81/jced-13-e211-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e87/7864363/f09f5df7b6fb/jced-13-e211-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e87/7864363/1d4486719559/jced-13-e211-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e87/7864363/6543a9083f81/jced-13-e211-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e87/7864363/f09f5df7b6fb/jced-13-e211-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e87/7864363/1d4486719559/jced-13-e211-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e87/7864363/6543a9083f81/jced-13-e211-g003.jpg

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本文引用的文献

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Necrotizing sialometaplasia can hide the presence of salivary gland tumors: A case series.坏死性涎腺化生可能会掩盖唾液腺肿瘤的存在:病例系列研究。
Oral Dis. 2019 May;25(4):1084-1090. doi: 10.1111/odi.13066. Epub 2019 Mar 5.
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Necrotizing sialometaplasia of the parotid gland associated with facial nerve paralysis.腮腺伴面神经瘫痪的坏死性涎腺化生。
J Stomatol Oral Maxillofac Surg. 2017 Feb;118(1):63-65. doi: 10.1016/j.jormas.2016.11.001. Epub 2017 Feb 3.
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Traumatic Ulcerative Granuloma with Stromal Eosinophila: A Case Report and Review of Pathogenesis.
伴基质嗜酸性粒细胞增多的创伤性溃疡性肉芽肿:一例报告及发病机制综述
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BMJ Case Rep. 2016 Aug 31;2016:bcr2016216621. doi: 10.1136/bcr-2016-216621.
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Contralateral recurrence of necrotizing sialometaplasia of the hard palate after five months: a case report.硬腭坏死性涎腺化生五个月后对侧复发:一例报告
J Korean Assoc Oral Maxillofac Surg. 2015 Dec;41(6):338-41. doi: 10.5125/jkaoms.2015.41.6.338. Epub 2015 Dec 17.
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Review of the literature on necrotizing sialometaplasia and case presentation.坏死性涎腺化生文献综述及病例报告
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Necrotizing sialometaplasia: A rare lesion that mimics oral cancer clinically and histopathologically.
Otolaryngol Pol. 2014 May-Jun;68(3):154-6. doi: 10.1016/j.otpol.2013.07.004. Epub 2013 Aug 5.
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Two rare entities in the same palate lesion: hyalinizing-type clear cell carcinoma and necrotizing sialometaplasia.同一腭部病变中的两种罕见实体:透明变性型透明细胞癌和坏死性涎腺化生。
J Craniofac Surg. 2014 May;25(3):e235-7. doi: 10.1097/SCS.0000000000000517.
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The clinical, histologic, and treatment spectrum in necrotizing sialometaplasia.坏死性涎腺化生的临床、组织学和治疗谱。
Oral Surg Oral Med Oral Pathol Oral Radiol. 2012 Nov;114(5):577-85. doi: 10.1016/j.oooo.2012.02.020. Epub 2012 Aug 22.
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