唾液腺分泌癌：一例小唾液腺病例及综述。

IF 1.8 3区医学 Q2 DENTISTRY, ORAL SURGERY & MEDICINE

Journal of Stomatology Oral and Maxillofacial Surgery Pub Date : 2024-09-28 DOI:10.1016/j.jormas.2024.102096

Elen de Souza Tolentino , Willian Pecin Jacomacci , Camila Camarini , Bruno Tavares Sedassari , Fabio Vieira de Miranda , Camila Lopes Cardoso

{"title":"唾液腺分泌癌：一例小唾液腺病例及综述。","authors":"Elen de Souza Tolentino , Willian Pecin Jacomacci , Camila Camarini , Bruno Tavares Sedassari , Fabio Vieira de Miranda , Camila Lopes Cardoso","doi":"10.1016/j.jormas.2024.102096","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction and importance</h3><div>Salivary gland secretory carcinoma (SGSC) represents a rare malignant tumor of the salivary glands. Despite being regarded as low-grade tumors, they may manifest with metastases and a high-grade aggressive clinical behaviour. The literature on this subject is limited, and there is currently no standardized approach to treatment.</div></div><div><h3>Case report</h3><div>We report a rare case of SGSC in the palate of a 14-year-old female patient. The patient underwent excision, bilateral tonsillectomy and adjuvant radiotherapy.</div></div><div><h3>Clinical discussion</h3><div>A critical review of the literature was conducted with the objective of analysing the cases of intraoral SGSC that have been previously reported. A total of 23 articles, published between 2010 and 2024, were identified as being directly pertinent to the review, resulting in a total of 58 patients being included.</div></div><div><h3>Conclusion</h3><div>SGSC on the hard palate in a 14-year-old child is an exceedingly rare occurrence. These tumors can mimic other pathologies of the salivary glands clinically and microscopically, which can result in misdiagnosis and a delay in treatment.</div></div>","PeriodicalId":55993,"journal":{"name":"Journal of Stomatology Oral and Maxillofacial Surgery","volume":"126 3","pages":"Article 102096"},"PeriodicalIF":1.8000,"publicationDate":"2024-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Salivary gland secretory carcinoma: A case presentation in minor salivary gland with review\",\"authors\":\"Elen de Souza Tolentino , Willian Pecin Jacomacci , Camila Camarini , Bruno Tavares Sedassari , Fabio Vieira de Miranda , Camila Lopes Cardoso\",\"doi\":\"10.1016/j.jormas.2024.102096\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction and importance</h3><div>Salivary gland secretory carcinoma (SGSC) represents a rare malignant tumor of the salivary glands. Despite being regarded as low-grade tumors, they may manifest with metastases and a high-grade aggressive clinical behaviour. The literature on this subject is limited, and there is currently no standardized approach to treatment.</div></div><div><h3>Case report</h3><div>We report a rare case of SGSC in the palate of a 14-year-old female patient. The patient underwent excision, bilateral tonsillectomy and adjuvant radiotherapy.</div></div><div><h3>Clinical discussion</h3><div>A critical review of the literature was conducted with the objective of analysing the cases of intraoral SGSC that have been previously reported. A total of 23 articles, published between 2010 and 2024, were identified as being directly pertinent to the review, resulting in a total of 58 patients being included.</div></div><div><h3>Conclusion</h3><div>SGSC on the hard palate in a 14-year-old child is an exceedingly rare occurrence. These tumors can mimic other pathologies of the salivary glands clinically and microscopically, which can result in misdiagnosis and a delay in treatment.</div></div>\",\"PeriodicalId\":55993,\"journal\":{\"name\":\"Journal of Stomatology Oral and Maxillofacial Surgery\",\"volume\":\"126 3\",\"pages\":\"Article 102096\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2024-09-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Stomatology Oral and Maxillofacial Surgery\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2468785524003847\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"DENTISTRY, ORAL SURGERY & MEDICINE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Stomatology Oral and Maxillofacial Surgery","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468785524003847","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}

引用次数: 0

摘要

导言和重要性：唾液腺分泌癌（SGSC）是一种罕见的唾液腺恶性肿瘤。尽管被认为是低级别肿瘤，但它们可能会出现转移和高级别侵袭性临床表现。这方面的文献很有限，目前也没有标准化的治疗方法：我们报告了一例罕见的腭部 SGSC 病例，患者为一名 14 岁女性。患者接受了切除术、双侧扁桃体切除术和辅助放疗：临床讨论：我们对文献进行了严格审查，目的是分析以前报道过的口腔内SGSC病例。共有23篇发表于2010年至2024年的文章被认为与该综述直接相关，共纳入58例患者：结论：14 岁儿童硬腭上的 SGSC 非常罕见。这些肿瘤在临床和显微镜下可与唾液腺的其他病变相似，从而导致误诊和治疗延误。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Salivary gland secretory carcinoma: A case presentation in minor salivary gland with review

Introduction and importance

Salivary gland secretory carcinoma (SGSC) represents a rare malignant tumor of the salivary glands. Despite being regarded as low-grade tumors, they may manifest with metastases and a high-grade aggressive clinical behaviour. The literature on this subject is limited, and there is currently no standardized approach to treatment.

Case report

We report a rare case of SGSC in the palate of a 14-year-old female patient. The patient underwent excision, bilateral tonsillectomy and adjuvant radiotherapy.

Clinical discussion

A critical review of the literature was conducted with the objective of analysing the cases of intraoral SGSC that have been previously reported. A total of 23 articles, published between 2010 and 2024, were identified as being directly pertinent to the review, resulting in a total of 58 patients being included.

Conclusion

SGSC on the hard palate in a 14-year-old child is an exceedingly rare occurrence. These tumors can mimic other pathologies of the salivary glands clinically and microscopically, which can result in misdiagnosis and a delay in treatment.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Journal of Stomatology Oral and Maxillofacial Surgery Surgery, Dentistry, Oral Surgery and Medicine, Otorhinolaryngology and Facial Plastic Surgery

CiteScore

2.30

自引率

9.10%

发文量

审稿时长

23 days