喉部纺锤形细胞癌:病例报告和文献综述。

IF 0.9 Q4 ONCOLOGY
Rare Tumors Pub Date : 2024-03-27 eCollection Date: 2024-01-01 DOI:10.1177/20363613241242705
Alia Mousli, Ferdaous Friaa, Emna Boudhina, Selma Kamoun, Rim Abidi, Chiraz Nasr
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引用次数: 0

摘要

简介纺锤形细胞癌(SCC)又称肉瘤样癌或癌肉瘤,是鳞状细胞癌的一种罕见变种,可累及包括喉部在内的多个器官。它是一种混合肿瘤,由恶性上皮细胞和间质细胞组成。由于喉部似乎是一个不常见的部位,我们报告了一例经过治疗的喉部 SCC,并对此类肿瘤进行了文献综述:患者为一名 72 岁男性,因发音障碍进行性加重已有 2 个月病史。患者的检查结果显示没有颈部腺病,而直接喉镜检查则发现前会厌有大量萌芽形成。对患者进行了活组织检查,发现是未分化癌。计算机断层扫描(CT)证实了声门肿瘤的存在,肿瘤完全阻塞了喉腔。PET-CT 检查未发现其他部位的转移。肿瘤被归类为 T3 N0 M0。患者接受了全喉切除术、甲状腺切除术和颈部切除术。最终组织病理分析确诊为喉癌,手术切缘阴性。随后,患者接受了肿瘤床辅助放疗(RT):原发性喉SCC是一种非常罕见的恶性肿瘤,在疾病的早期阶段容易发生控制侧淋巴结转移。由于其侵袭性较强,建议将手术和术后 RT 结合使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spindle cell carcinomaof the larynx: A case report and literature review.

Introduction: Spindle cell carcinoma (SCC), also called sarcomatoid carcinoma or carcinosarcoma, represents a rare variant of squamous cell carcinoma that may involve multiple organs, including the larynx. It is a mixed tumor, composed of both malignant epithelial and mesenchymal elements. As the larynx appears to be an unusual site, we report a case of treated SCC laryngeal as well as a literature review of such tumor.

Observation: A 72-year-old male, with 2 months' history of a progressive worsening dysphonia, was examined. The patient examination showed no cervical adenopathy, while direct laryngoscopy detected a voluminous budding formation of the anterior commissure. A biopsy was performed, in which an undifferentiated carcinoma was identified. The computed tomography (CT) confirmed the existence of a glottic tumor, which completely obstructs the lumen of the larynx. No metastasis were noticed elsewhere on the PET-CT. The tumor was then classified as T3 N0 M0. The patient underwent a total laryngectomy, thyroidectomy and neck dissection. The definitive histopathological analysis confirmed the diagnosis of SCC of the larynx with negative surgical margins. Afterward, the patient underwent adjuvant radiotherapy (RT) on the tumor bed.

Conclusion: Primary laryngeal SCC is a very rare malignancy with a tendency to occur with controlateral lymph node metastasis at an early stage of the disease. Combining surgery and postoperative RT is recommended due to its aggressive profile.

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Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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