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9例成人横纹肌肉瘤的临床病理学分析 被引量:1

Clinicopathologic features of 9 cases of adult rhabdomyosarcoma
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摘要 目的·探讨成人横纹肌肉瘤(RMS)的临床病理特点及预后。方法·回顾性分析9例RMS患者临床和病理资料,及免疫组织化学检测结果。结果·该组患者平均年龄(46.89±20.09)岁,其中男性6例,女性3例。肿瘤分布范围广。组织学亚型包括胚胎性RMS 6例,腺泡状RMS、多形性RMS和梭形细胞RMS各1例。免疫组织化学检测结果显示,横纹肌标记阳性例数分别为肌细胞生成蛋白阳性6例、肌调节蛋白阳性4例、结蛋白阳性8例。7例随访中无瘤生存仅2例,带瘤生存(均为术后出现复发或转移)2例,死于肿瘤3例。结论·该组成人RMS病例中以胚胎性RMS最常见,免疫组织化学检测有助于RMS的诊断。 Objective · To investigate the clinicopathologic characteristics and prognosis of adult rhabdomyosarcoma (RMS). Methods · The clinical and pathological data, immunohistochemical test results of 9 RMS were analyzed retrospectively. Results · The information of 6 males and 3 females were collected in this research, whose average age was (46.89±20.09) years old. The tumors had a wide range distribution. The subtypes of histology included 6 cases of embryonal RMS, 1 case of alveolar RMS, 1 case of spindle cell RMS and 1 case of pleomorphic RMS. Immunohistochemically study showed that 6 cases were myogenin positive, 4 cases were MyoD1 positive and 8 cases were desmin positive. During the follow-up period of the 7 cases, only 2 patients survived free of tumors, 2 patients presented with tumor recurrence and metastasis after the operations, and 3 patients died of tumor. Conclusion · In this study, embryonal RMS is the most common type, and immunohistochemistry test is helpful to diagnosis of RMS.
出处 《上海交通大学学报(医学版)》 CSCD 北大核心 2017年第7期1015-1019,共5页 Journal of Shanghai Jiao tong University:Medical Science
关键词 横纹肌肉瘤 成人 临床病理学 免疫组织化学 诊断 预后 rhabdomyosarcoma adult clinicopathology immunohistochemistry diagnosis prognosis
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  • 1吴位育,北京第二医学院学报,1985年,6卷,137页
  • 2Miettinen M. Rhabdomyosarcoma in patients older than 40 years of age. Cancer, 1988, 62:2060-2065.
  • 3Stock N, Chibon F, Binh MB, et al. Adult-type rhabdomyosarcoma: analysis of 57 cases with clinicopathologic description, identification of 3 morphologic patterns and prognosis. Am J Surg Pathol, 2009, 33 : 1850-1859.
  • 4Fletcher CDM, Unni KK, Mertens F. World Health Organization Classification of Tumours Pathology and Genetics of Tumours of Soft Tissue and Bone. Lyon: IARC Press, 2007:146-154.
  • 5Folpe AL, McKenney JK, Bridge JA, et al. Sclerosing rhabdomyosareonn in adults : report of four cases of a hyalinizing, matrix-rich variant of rhabdomyosarcoma that may be confused with osteosarcoma, chondrosarcoma, or angiosarcoma. Am J Surg Pathol, 2002, 26 : 1175-1183.
  • 6Jo VY, Marino-Enrtquez A, Fletcher CD. Epithelioid rhabdomyosarcorm: clinicopathologic analysis of 16 cases of a morphologically distinct variant of rhabdomyosarcoma. Am J Surg Pathol, 2011,35:1523- 1530.
  • 7Perez-Ordonez B, Kandel RA, Bell R, et al. Rhabdomyosarcoma with rhabdoid-like features. Pathol Res Pract, 1998, 194:357- 361.
  • 8Hawkins WG, Hoos A, Antonescu CR, et al. Clinicopathologic analysis of patients with adult rhabdomyosarcoma. Cancer, 2001, 91:794-803.
  • 9Stout AP. Rhabdomyosarcoma of skeletal muscles. Ann Surg, 1946, 123:447--472.
  • 10Ferrari A, Dileo P, Casanova M, et al. Rhabdomyosarcoma in adults. A retrospective analysis of 171 patients treated at a single institution. Cancer, 2003, 98:571-580.

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