期刊文献+

成人头颈部原发性软组织肉瘤2例

A case report of adult primary soft tissue sarcoma of the head and neck
原文传递
导出
摘要 头颈部原发性软组织肉瘤是成人罕见的来源于间叶组织的结缔组织恶性肿瘤,可发生于鼻旁窦、咽喉或颈部间隙内,临床表现为头颈部局部蔓延性肿物或呼吸、吞咽困难等,MRI和增强CT检查为此类疾病最常用的检查手段,病理诊断需要免疫组织化学结合荧光原位杂交技术(FISH)检测MDM2和CDK4作为常规辅助手段,本文分别报道腮腺高分化脂肪肉瘤和喉去分化平滑肌肉瘤各1例,介绍其病例特点和诊治经过,并对该病例进行相关文献复习。 Head and neck primary soft tissue sarcoma is a rare adult connective tissue malignant tumor derived from mesenchymal tissue,which can occur in the paranasal sinuses,throat or neck space.The clinical manifestations are local spread masses in the head and neck or difficulty breathing,swallowing,etc al.MRI and enhanced CT examination are the most commonly used to diagnose such diseases.Pathological diagnosis requires immunohistochemistry combined with FISH to detect MDM2 and CDK4.In this report,two cases of primary soft tissue sarcoma were reported,one is parotid high-differentiated liposarcoma and the other is laryngeal dedifferentiated leiomyosarcoma,introducing the characteristics diagnosis and treatment,and reviewing the relevant literature.
作者 刘磊峰 邱海涛 惠明朗 江枫 王代红 林玉英 杨新建 姚俊 LIU Leifeng;QIU Haitao;HUI Minglang;JIANG Feng;WANG Daihong;LIN Yuying;YANG Xinjian;YAO Jun(Department of Otolaryngology Head and Neck Surgery,Affiliated Hospital of Guangdong Medical University,Zhanjiang,524000,China;Graduate School of Guangdong Medical University)
出处 《临床耳鼻咽喉头颈外科杂志》 CAS CSCD 北大核心 2023年第2期146-149,共4页 Journal of Clinical Otorhinolaryngology Head And Neck Surgery
关键词 头颈部肿瘤 脂肪肉瘤 平滑肌肉瘤 head and neck neoplasms liposarcoma leiosarcoma
  • 相关文献

参考文献2

二级参考文献28

  • 1Fletcher CDM,Unni K,Mertens M.Word Health Organization classification of tumours.Pathology and genetics of tumors of softtissue and bone[M].Lyon:IARC Press,2002.14-46.
  • 2Collins K,Jacks T,Pavletich NP.The cell cycle and cancer[J].Proc Natl Acad Sci U S A,1997,94(7):2776-2778.
  • 3Baker SJ.A role for Cdk4 in angiogenesis[J].Cell Cycle,2010,9(13):2493.
  • 4Fletcher CD,Akerman M,Dal Cin P,et al.Correlation betweenclinicopathological features and karyotype in lipomatous tumors.Areport of 178 cases from the Chromosomes and Morphology(CHAMP)Collaborative Study Group[J].Am J Pathol,1996,148(2):623-630.
  • 5Pilotti S,Della Torre G,Lavarino C,et al.Molecularabnormalities in liposarcoma:role of MDM2 and CDK4-containing amplicons at 12q13-22[J].J Pathol,1998,185(2):188-190.
  • 6Micci F,Teixeira MR,Bjerkehagen B,et al.Characterization ofsupernumerary rings and giant marker chromosomes in well-differentiated lipomatous tumors by a combination of G-banding,CGH,M-FISH,and chromosome-and locus-specific FISH[J].Cytogenet Genome Res,2002,97(1-2):13-19.
  • 7Schneider-Stock R,Walter H,Radig K,et al.MDM2amplification and loss of heterozygosity at Rb and p53 genes:nosimultaneous alterations in the oncogenesis of liposarcomas[J].JCancer Res Clin Oncol,1998,124(10):532-540.
  • 8Sirvent N,Coindre JM,Maire G,et al.Detection of MDM2-CDK4 amplification by fluorescence in situ hybridization in 200paraffin-embedded tumor samples:utility in diagnosing adipocyticlesions and comparison with immunohistochemistry and real-timePCR[J].Am J Surg Pathol,2007,31(10):1476-1489.
  • 9Dal Cin P,Sciot R,Panagopoulos I,et al.Additional evidenceof a variant translocation t(12;22)with EWS/CHOP fusion inmyxoid liposarcoma:clinicopathological features[J].J Pathol,1997,182(4):437-441.
  • 10Hosaka T,Nakashima Y,Kusuzaki K,et al.A novel type ofEWS-CHOP fusion gene in two cases of myxoid liposarcoma[J].JMol Diagn,2002,4(3):164-171.

共引文献14

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