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. 2017 May 7;52(5):385-387.
doi: 10.3760/cma.j.issn.1673-0860.2017.05.013.

[Clinic features of laryngeal carcinosarcoma and sarcomatoid carcinoma]

[Article in Chinese]
Affiliations

[Clinic features of laryngeal carcinosarcoma and sarcomatoid carcinoma]

[Article in Chinese]
Y J Li et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. .

Abstract

Objective: To investigate the clinic feature, pathology, therapy and prognosis of the sarcomatoid caricinoma or carcinosarcoma of the larynx. Methods: We reviewed the clinical records of 7 patients with laryngeal carcinosarcoma /sarcomatoid caricinoma who were treated at our hospital between June 1996 and August 2016. All patients were men (mean age, 65.9 years; range, 52 to 94 years). Among 7 patients, 6 had a history of smoking; 2 underwent radiotherapy; and 5 patients who didn't undergo radiotherapy complained of hoarseness. The glottis was the most frequent site of involvement. Most tumors exhibited a polypold or pedunculated gross morphology. Among the 5 patients who didn't undergo a radiotherapy, 2 were in stage Ⅰ, 2 in stageⅡ, and 1 in stage Ⅲ. The other 2 cases underwent surgeries and radiotherapy were staged. Results: All 7 patients received surgeries, without lymph node metastasis. All the tumors were pathologically carcinosarcoma/sarcomatoid carcinoma. With immunohistochemistry examination, Vimetin was positive in all tumors, SMA positive in 3 tumors, S-100 positive in 1 tumors, but CD-68, HMB-45 or Myglobin was negative in all tumors. With follows-up from 3 months to 20 years, of 7 patients, 4 survived without recurrent, 1 dead, and 2 lost connection. Conclusions: Both of the carcinosarcoma and the sarcomatoid carcinoma of larynx contain pathologically carcinoma and sarcoma. Surgery is the best choice for laryngeal sarcomatoid carcinoma, and these patients without a undergoing radiotherapy before surgery or these with little sarcoma in tumors show better prognosis.

目的: 探讨喉肉瘤样癌及癌肉瘤的临床特征、病理表现、治疗手段及预后。 方法: 回顾性分析1996年6月至2016年4月中国医学科学院北京协和医学院北京协和医院耳鼻咽喉科7例病理证实的原发于喉的肉瘤样癌或者癌肉瘤临床病例资料。7例患者均为男性,平均发病年龄65.9岁,6例有长期吸烟史,其中2例有喉部放疗病史;未前期治疗的5例患者均以声音嘶哑为首发症状;主要原发部位均位于声门区域,典型喉镜表现为表面基本光滑的息肉样或菜花样新生物;就诊时肿瘤分期Ⅰ期2例,Ⅱ期2例,Ⅲ期1例,另外2例均为喉癌手术+放疗后复发患者,不适合分期。 结果: 患者均手术治疗,均无淋巴结转移。术后病理报告为肉瘤样癌或癌肉瘤,病理显示肿物为癌和肉瘤样成分并存,癌成分为鳞状细胞癌,肉瘤成分表现为杂乱排列的梭形细胞,免疫组化显示肿瘤组织Vimetin强阳性,SMA阳性3例,CD68阳性0例,S-100阳性1例,均无HMB-45及Myglobin表达。随访3个月至20年,其中死亡1例,失访2例,其余4例患者目前均存活。 结论: 喉部肉瘤样癌或癌肉瘤光镜下都可见到癌及肉瘤成分,肉瘤样癌分子水平研究显示该类肿瘤为单克隆的上皮性肿瘤,伴有间叶趋异进化,手术为主要治疗手段,无前期放疗病史及肉瘤样成分侵入较浅者预后良好。.

Keywords: Larynx, carcinosarcoma; Sarcomatoid carcinoma; Spindle cell carcinoma.

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