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性腺外恶性生殖细胞肿瘤37例临床病理分析 被引量:5

Malignant extragonadal germ cell tumors: a clinicopathologic analysis of 37 cases
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摘要 目的 探讨性腺外恶性生殖细胞肿瘤的病理类型和临床特点。方法 根据WHO肿瘤国际组织学分类(第 2版 )对 37例性腺外恶性生殖细胞肿瘤重新评价 ,部分病例做相应免疫组化染色 ,并将肿瘤的组织类型和临床特点与性腺恶性生殖细胞肿瘤进行比较分析。结果 患者年龄 1 5~ 5 8岁 ,中位年龄 2 4岁。男性 2 8人 ,女性 9人 ,男女之比为 3 1∶1。发生于纵隔 2 8例 ,腹膜后 5例 ,前列腺、骶尾部、鞍区、阴道各 1例。列前三位的肿瘤分别是卵黄囊瘤、畸胎瘤 (未成熟畸胎瘤、PNET和畸胎瘤恶变 )和精原细胞瘤 ,另有 5例为混合型生殖细胞瘤。结论 性腺外恶性生殖细胞肿瘤相对少见 ,预后差 ,发病率与年龄、性别关系密切 ,好发部位为纵隔和腹膜后 ,卵黄囊瘤最为多见。 Objective To investigate clinicopathologic characteristics of malignant extragonadal germ cell tumors. Methods 37 cases of malignant extragonadal germ cell tumor (MEGGCT) in the files of CAMS Cancer Hospital were reviewed and reclassified according to the criteria of WHO histological classification of ovarian tumors (2nd edition). Clinicopathologic features including treatment and prognosis were reevaluated in comparison with malignant gonadal germ cell tumors (MGGCT). Results The age of the patients ranged from 1.5 to 58 years (median 24), 28 male and 9 female, M/F ratio was 3.1∶1 in the tumors arisen in mediastinum, 5 in retroperitneum, 1 in prostate, sacrococcygeal area, pineal area and vagina respectively. Histologically, 14 were yolk sac tumor, 5 immature teratoma, 5 seminoma, 2 PNET, and 2 mature cystic teratoma with malignant transformation. The rest were mixed germ cell tumor and embryonal carcinoma. Conclusions MEGGCT is relatively rare, mostly often occurs in the mediastinum and the retroperitneum. There is a close relationship between age, sex and incidence of MEGGCT. Yolk sac tumor is at the top of the list. The prognosis is worse than those occurred in gonads.
出处 《诊断病理学杂志》 CSCD 2003年第1期14-16,I004,共4页 Chinese Journal of Diagnostic Pathology
关键词 性腺外恶性生殖细胞肿瘤 病理 外科学 免疫组化染色 Extragonadal germ cell tumor Pathology Surgery
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  • 1阿克曼 回允中主译.阿克曼外科病理学:第8版[M].沈阳:辽宁教育出版社,1999.494.
  • 2李凌 张洵.卵巢肿瘤病理学类型[A]..见:中国肿瘤病理学分类第22分册[C].北京:科学技术文献出版社,2001.535.

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