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横纹肌肉瘤的临床病理分析 被引量:2

PATHOLOGIC STUDY ON RHABDOMYOSARCOMA
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摘要 目的 :探讨横纹肌肉瘤的诊断和鉴别诊断中免疫组织化学标记的意义及不同类型横纹肌肉瘤对预后的影响。方法 :应用病理形态学和免疫组化方法对 47例横纹肌肉瘤进行研究。结果 :47例横纹肌肉瘤中胚胎性 2 8例 ,腺泡状 16例 ,其中 7例伴广泛侵润、复发和转移 ,多型性 3例 ;结蛋白 (desm in)和肌球蛋白 (m yoglobin)的阳性率分别为 (89% )和 (83.2 % )。结论 和胚胎性横纹肌肉瘤相比 ,腺泡状横纹肌肉瘤具有更恶的临床生物学行为 ;desm To search for the significance of immunohistochemical markers for the differential diagnosis of rhabdomyosarcoma and the clinical impact of different subtypes of rhabdomyosarcoma on prognosis. Method:Pathomorphological and immunohistichemical methods were used for study of 47 cases of rhahdomyosarcoma Results:Of the 47 cases,28 cases are embryonal rhabdomyosarcoma,16 cases of alveolar rhabdomyosarcoma,seven of whom were accompanied by extensive invasiveness,recurrence and metastasis,3 cases showed polymorphism,higher positive rates of desmin(89%)and myoblobin(83.2%) were found in rhabdomyosarcoma.Conclusion:The clinical behavior in alveolar rhabdomyosarcoma is more malign than that in embryonal rhabdomyosarcoma,desmin and myoglobin turned out to be a favorite markers for the differential diagnosis of rhabdomyosarcoma
出处 《锦州医学院学报》 CAS 2000年第2期1-4,共4页 Journal of Jinzhou Medical College
关键词 横纹肌肉瘤 病理学 结蛋白 肌球蛋白 rhabdomyosaroma pathology
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  • 1何乐健,王琳,孙宁,黄澄如,祝秀丹,郎志奇.儿童横纹肌肉瘤的临床病理研究[J].中华病理学杂志,2004,33(3):225-228. 被引量:40
  • 2Goldstein M, Meller I, Issakov J, et al. Novel genes implicated in embryonal, alveolar, and pleomorphic rhabdomyosarcoma: a cytogenetic and molecular analysis of primary tumors [ J 1. Neoplasia, 2006,8 (5) :332-343.
  • 3Schaaf GJ, Ruijter JM, van Ruissen F, et al. Full transcnptome analysis of rhabdomyosarcoma, normal, and fetal skeletal muscle: statistical comparison of multiple SAGE libraries [ J ]. FASEB J, 2005,19(3) :404-406.
  • 4Hanks S, Coleman K, Summersgill B,et al. Comparative genomic hybridization and BUB1 B mutation analyses in childhood cancers associated with mosaic variegated aneuploidy syndrome [ J ]. Cancer Left,2006,239 (2) :234-238.
  • 5Duesberg P, Fabarius A, Hehlmann R. Aneuploidy, the primary cause of the multilateral gcnomic instability of neoplastic and preneoplastic cells[J]. IUBMB Life,2004,56(2) :65-81.
  • 6Ragazzini P,Gamberi G,Pazzaglia L,et al. Amplification of CDK4, MDM2, SAS and GLI genes in leiomyosarcoma, alveolar and embry- onal rhabdomyosarcoma [ J ]. Histol Histopathol, 2004, 19 ( 2 ) : 401-411.
  • 7Kilpatrick SE, Teot LA, Geisinger KR, et al. Relationship of DNA ploidy to histology and prognosis in rhabdomyosarcoma. Comparison of flow cytometry and image analysis [ J ]. Cancer, 1994,74 (12): 3227-3233.
  • 8Kratz CP, Steinemann D, Niemeyer CM, et al. Uniparental disomy at chromosome 11 p15.5 followed by HRAS mutations in embryonal rhabdomyosarcoma :lessons from Costello syndrome [ J ]. Hum Mol Genet, 2007,16 ( g ) : 374-379.
  • 9Bridge JA, Liu J, Weiboh V, et al. Novel genomic imbalances in embryonal rhabdomyosarcoma revealed by comparative genomic hy- bridization and fluorescence in situ hybridization: an intergroup rhabdomyosarcoma study [ J ]. Genes Chromosomes Cancer, 2000, 27(4) :337-344.
  • 10Ho RH,Johnson J,Dev VG,et al. A novel t(2;20) (q35;p12) in embryonal rhabdomyosarcoma[ J]. Cancer Genet Cytogenet,2004, 151 ( 1 ) :73-77.

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