期刊文献+

喉部未分化软组织肉瘤1例并文献复习

Laryngeal undifferentiated soft-tissue sarcoma:a case report and review of literature
原文传递
导出
摘要 1病例报告患者,男,74岁,因“声嘶1月余”首次入院,伴有咳嗽、咳白色黏痰,偶有气促,无痰中带血、发热、乏力,无反酸、烧心,无咽部异物感,无吞咽困难等。既往吸烟、饮酒史60年。电子喉镜示前连合肿物,大小约1.0cm×0.5cm×0.5cm,呈哑铃状,部分脱入声门下(图1a)。于全身麻醉显微支撑喉镜下行喉肿物切除术,术后病理及免疫组织化学倾向于炎性肌纤维母细胞瘤(图1b)。 Patient presented as a 74-year-old male complaining of hoarseness. Electronic laryngoscope showed a neoplasm whose size was about 1.0 cm×0.5 cm×0.5 cm at anterior commissure. A surgery was con- ducted to excise the neoplasm en bloc. The histopathologieal and immunohistochemistry examination suggested in- flammatory myofibroblastic tumor. A month later, the patient presented with dyspnea and blood-stained sputum. CT scan of neck showed an occupation lesions under glottis. A tracheotomy and a CO2 laser surgery was conducted due to patients will. The histopathological and immunohistochemistry examination suggested undifferentiated sar- coma. We advised him keeping a tracheal cannula to receive further treatment such as radiotherapy or chemothera- py in ontology department, but the patient was not compliant with care instructions for personal reason. He was readmitted 2 months later for dyspnea after plugging the tube. Electronic laryngoscope showed a large neoplasm occupied the laryngeal vestibule, covering the glottis. CT and MRI scan showed the lesion involved spaces of supra- glottic, glottic, subglottic and soft tissue around larynx. Hence, a total laryngotomy and bilateral functional neck dissection was conducted. The histopathological examination agreed with the former one. Three weeks later, the skin around his tracheal cannula swelled, ulcerated and pyorrheal. After 10 days of dressing change, patient died of uncontrolled infection.
出处 《临床耳鼻咽喉头颈外科杂志》 CAS 北大核心 2017年第15期1205-1208,共4页 Journal of Clinical Otorhinolaryngology Head And Neck Surgery
基金 北京教委面上项目(No:KM201510025026) 北京友谊医院启动课题(No:yyqdkt2014-23) 北京友谊医院启动课题(No:yydszx2015-02)
关键词 头颈部肿瘤 软组织肉瘤 诊断 治疗 head and neck neoplasms soft-tissue sarcoma diagnosis therapy
  • 相关文献

参考文献4

二级参考文献37

  • 1孟黎平,黄志纯,姚青,冯旭,顾建兴,冯立人,朱新.头颈部炎性肌纤维母细胞瘤[J].中国耳鼻咽喉头颈外科,2006,13(1):5-7. 被引量:15
  • 2Hiroshi Koide,Ken Sato,Toshio Fukusato,Kenji Kashiwabara,Noriaki Sunaga,Takafumi Tsuchiya,Saeko Morino,Naondo Sohara,Satoru Kakizaki,Hitoshi Takagi,Masatomo Mori.Spontaneous regression of hepatic inflammatory pseudotumor with primary biliary cirrhosis:Case report and literature review[J].World Journal of Gastroenterology,2006,12(10):1645-1648. 被引量:13
  • 3EM López-Tomassetti Fernández,H Díaz Luis,A Martín Malagón,I Arteaga González,A Carrillo Pallarés.Recurrence of inflammatory pseudotumor in the distal bile duct: Lessons learned from a single case and reported cases[J].World Journal of Gastroenterology,2006,12(24):3938-3943. 被引量:7
  • 4曹海光,刘素香.炎性肌纤维母细胞瘤[J].中国肿瘤临床,2007,34(13):776-779. 被引量:48
  • 5Weiss SW, Enzinger FM. Malignant fibrous histiocytoma: An analysis of 200 cases[J]. Cancer, 1972, 29 : 961 - 976.
  • 6Tos AP. Classification of pleomorphic sarcomas: where are we now? [ J]. Histopathology, 2006, 48:52-62.
  • 7Fletcher CDM. Pleomorphic malignant fibrous histiocytoma: fact of fiction? A critical reappraisal of 159 tumors diagnosed as pleomorphic sarcomas [ J ]. Am J Surg Pathol, 1992, 16 : 213 - 228.
  • 8Fletcher CDM, Coindre JM, Molenaar WM, et al. So-called fibrohistiocytic tumors [M]//Fletcher CDM, Unni KK, Mertens F. World Health Organization classification of tumours. Pathology and genetics of tumors of soft tissue and bone. Lyon: IARC Press, 2002 : 109 - 126.
  • 9O' Brien JE, Stout AP. Malignant fibrous xanthomas[ J ]. Cancer, 1964, 17 : 1445 - 1455.
  • 10Fletcher CDM, Gustafson P, Rydholm A, et al. Clinicopathologic re-evaluation of 100 malignant fibrous histiocytomas: prognostic relevance of subclassification [ J]. J Clin Oncol, 2001, 19: 3045 - 3050.

共引文献97

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部