颌下腺导管癌的综合诊断与治疗:1例报告并文献复习。

IF 1.1 Q4 ONCOLOGY
Feng Liu, Li Fan, Lifang Lu, Hongyi Guo, Jie Nan, Fei Han
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引用次数: 0

摘要

涎腺导管癌(SDC)是一种罕见的涎腺恶性肿瘤,最常见于腮腺,其次是下颌腺。由于其罕见,对其治疗尚无共识。手术切除是目前唯一有效的治疗方法。鉴于其恶性程度高,建议广泛切除肿瘤并术后辅助放疗。我们报告一个罕见的颌下腺SDC病例。男性62岁,主诉右侧上颌下区肿胀4个月,快速增长,疼痛10天。入院后,细针抽吸(FNA)显示右侧颌下腺导管癌。考虑到其侵袭性,体积大,侵犯咽旁及口腔底软组织,患者接受了两个周期的新辅助化疗,然后延长手术切除。术后,患者接受4个周期同步放化疗,随后接受阿法替尼靶向治疗。在45个月的随访中未见复发或转移。因此,我们提出了一种新辅助化疗联合手术、术后同步放疗、化疗加阿法替尼靶向治疗的涎腺导管癌综合治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive diagnosis and treatment of ductal carcinoma of the submandibular gland: case report and literature review.

Salivary duct carcinoma (SDC) is a rare malignant tumor of the salivary gland and is most commonly found in the parotid gland, followed by the submandibular gland. Due to its rarity, there is no consensus on its treatment. Surgical resection is currently the only curative treatment. Considering its high degree of malignancy, extensive tumor resection and postoperative adjuvant radiotherapy are recommended. We report a rare case of SDC of the submandibular gland. A 62-year-old man presented to our hospital with complaints of swelling in the right submaxillary area for 4 months, rapidly growing, with pain for 10 days. After admission, fine needle aspiration (FNA) revealed right submandibular gland ductal carcinoma. Considering its aggressiveness, large size, and invasion of parapharyngeal and oral floor soft tissues, the patient received two cycles of neoadjuvant chemotherapy followed by extended surgical resection. Postoperatively, the patient received four cycles of concurrent chemoradiotherapy, followed by afatinib targeted therapy. No recurrence or metastasis was observed in a 45-month follow-up. Thus we present a comprehensive treatment for salivary duct carcinoma combining neoadjuvant chemotherapy with surgery, postoperative concurrent radiotherapy, and chemotherapy followed by afatinib targeted therapy.

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来源期刊
自引率
0.00%
发文量
42
审稿时长
1 months
期刊介绍: The International Journal of Clinical and Experimental Pathology (IJCEP, ISSN 1936-2625) is a peer reviewed, open access online journal. It was founded in 2008 by an international group of academic pathologists and scientists who are devoted to the scientific exploration of human disease and the rapid dissemination of original data. Unlike most other open access online journals, IJCEP will keep all the traditional features of paper print that we are all familiar with, such as continuous volume and issue numbers, as well as continuous page numbers to keep our warm feelings towards an academic journal. Unlike most other open access online journals, IJCEP will keep all the traditional features of paper print that we are all familiar with, such as continuous volume and issue numbers, as well as continuous page numbers to keep our warm feelings towards an academic journal.
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