期刊文献+

口腔颌面部尤文肉瘤的影像学和病理学特点(英文) 被引量:2

Image and pathological features of Ewing's sarcoma in the oral and maxillofacial region
下载PDF
导出
摘要 目的:系统研究口腔颌面部尤文肉瘤的影像学和病理学特点。方法:将8名患有口腔颌面部尤文肉瘤的患者纳入本研究,并系统评价其X线、CT和MRI图像特征及病理学特点。结果:X线结果显示颌骨尤文肉瘤表现为弥漫性、透射性的囊性结构,边界不清。CT结果显示颌骨肉瘤表现为骨质广泛性破坏并且有溶骨性病变,同时侵犯软组织,但没有骨膜反应。MRI结果显示颌骨尤文肉瘤组织的信号不均匀,边界不清楚同时侵犯相邻的软组织。软组织尤文肉瘤的MRI图像与颌骨尤文肉瘤的MRI表现相似。组织学结果显示尤文肉瘤由小圆细胞组成,并表达CD99、神经元特异性烯醇化酶(NSE)和波形蛋白(Vimentin),不表达Des,CD34,上皮膜抗原(epithelial membrane antigen,EMA)和嗜铬粒蛋白A(chromogranin A,Chg A)等标志物。结论:X线、CT及MRI有助于确定尤文肉瘤的性质、与周围组织的关系及侵犯程度。CD99,NSE和Vimentin免疫组织化学染色有助于尤文肉瘤的病理诊断。 Objective: To systematically evaluate the image and pathological features of Ewing's sarcoma (ES) in the oral and maxillofacial region. Methods: Eight patients with ES in the oral and maxillofacial region were enrolled for this study. The X-ray3 computed tomography (CT), and magnetic resonance imaging (MRI) of ES and the pathological data were systematically evaluated. Results: X-ray image showed a diffuse radiolucency with cystic component and ill-defined borders for bone lesion. CT showed that there was osteolytic mass with extensive bone destruction and soft tissue infiltration, but no periosteal reactions were observed. MRI demonstrated that ES showed an inhomogeneous structure and blurred borders with invasion to adjacent soft tissue for bone lesion. Similar manifestation also showed in MRI images for patients with soft tissues. Histologically) ES composed of small round cells, and expressed CD99, neuron specific enolase (NSE) and vimentin (Vim) in all patients. Desmin (Des), CD34, epithelial membrane antigen (EMA), chromogranin A (ChgA), etc, were negatively expressed in ES cells. Conclusion- X-ray) CT, and MRI are helpful to determine the property, extent and the relationship orES with the surrounding tissues. Immunohistochemical stain of CD99, NSE, and Vim are helpful to confirm the pathological diagnosis orES.
出处 《中南大学学报(医学版)》 CAS CSCD 北大核心 2016年第6期637-643,共7页 Journal of Central South University :Medical Science
基金 supported by the Department of Pathology, The Second Xiangya Hospital of Central South University, China
关键词 影像 病理 尤文肉瘤 口腔颌面部 image pathology Ewing's sarcoma oral and maxillofacial region
  • 引文网络
  • 相关文献

参考文献19

  • 1Tanaka M, Yamazaki Y, Kanno Y, et al. Ewing's sarcoma precursors are highly enriched in embryonic osteochondrogenic progenitors [J]. J CIin Invest, 2014, 124(7): 3061-3074.
  • 2Talesh KT, Motamedi MH, Jeihounian M. Ewing's sarcoma of the mandibular condyle: report of a case [J]. J Oral Maxillofac Surg, 2003, 61(10): 1216-1219.
  • 3Gosau M, Baumhoer D, Ihrler S, et al. Ewing sarcoma of the mandible mimicking an odontogenic abscess- a case report[J]. Head Face Med, 2008, 4: 24.
  • 4Allam A, E1-Husseiny G, Khafaga Y, et al. Ewing's sarcoma of the head and neck: a retrospective analysis of 24 cases[J]. Sarcoma, 1999, 3(1):11-15.
  • 5Kuleta-Bosak E, Kluczewska E, Machnik-Broncel J, et al. Suitability of imaging methods (X-ra)5 C2, MRI) in the diagnostics of Ewing's sarcoma in children-analysis of own material[J]. Pol J Radiol, 2010, 75(1): 18-28.
  • 6Li WY, Brock P, Saunders DE. Imaging characteristics of primary cranial Ewing sarcoma[J]. Pediatr Radiol, 2005, 35(6): 612-618.
  • 7Desai SS, Jambhekar NA. Pathology of Ewing's sarcoma/PNET: Current opinion and emerging concepts[J]. Indian J Orthor, 2010, 44(4): 363-368.
  • 8Pinto A, Dickman P, Parham D. Pathobiologic markers of the ewing sarcoma family of tumors: state of the art and prediction of behaviour[J]. Sarcoma, 2011, 2011: 856190.
  • 9Hu-Lieskovan S, Zhang J, Wu L, et al. EWS-FL11 fusion protein up- regulates critical genes in neural crest development and is responsible for the observed phenotype of Ewing's family of tumors [J]. Cancer Res, 2005, 65(11): 4633-4644.
  • 10Tirode F, Laud-Duval K, Prieur A, et al. Mesenchymal stem cell features of Ewing tumors[J]. Cancer Cell, 2007, 11(5): 421-429.

同被引文献21

引证文献2

二级引证文献2

;
使用帮助 返回顶部