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Clinical outcome after retroperitoneal lymphadenectomy of patients with pure testicular teratoma.

机译:单纯睾丸畸胎瘤患者腹膜后淋巴结清扫术的临床结果。

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OBJECTIVES: To determine the pathologic findings and clinical outcome of patients with pure teratoma of the testis who underwent primary or postchemotherapy retroperitoneal lymphadenectomy (RPLND). METHODS: From January 1989 to February 1998, 29 patients with pure testicular teratoma underwent primary (n = 11) or postchemotherapy (n = 18) RPLND. RESULTS: Overall, 23 (79%) of 29 patients had retroperitoneal disease, with 18 (62%) initially presenting with advanced disease. The pathologic stage in the 11 patients undergoing primary RPLND was pN0 in 6 (55%), pN1 in 3 (27%), and pN2 in 2 (18%). Of the 7 patients with clinical Stage I undergoing primary RPLND, 1 had teratoma and 1 had seminoma in the retroperitoneum; of the 4 patients with clinical Stage IIA, 2 had teratoma and 1 had embryonal carcinoma. Four patients were lost to follow-up and the other seven had no evidence of disease (NED) at a median follow-up of 90.4 months, with no relapses. The pathologic findings in the 18 patients undergoing postchemotherapy RPLND revealed fibrosis in 8, teratoma in 9, and yolk sac tumor in 1. At last follow-up, 7 of the 9 patients with teratoma were NED, 1 was dead of disease, and 1 was dead of unknown causes. Of the 8 patients with fibrosis, 6 had NED and 2 were lost to follow-up. The patient with viable cancer had NED at last follow-up. CONCLUSIONS: These data underscore the metastatic potential of pure testicular teratoma. A significant proportion (45%) of patients with low-stage pure testicular teratoma had retroperitoneal disease. Furthermore, a high proportion (62%) presented initially with advanced disease and demonstrated a considerable risk of relapse despite complete resection or favorable histologic features in the resected retroperitoneal specimen.
机译:目的:确定接受原发性或化疗后腹膜后淋巴结清扫术(RPLND)的纯睾丸畸胎瘤患者的病理结果和临床结果。方法:从1989年1月至1998年2月,对29例纯睾丸畸胎瘤患者进行了原发性(n = 11)或化疗后(n = 18)的RPLND。结果:总共29例患者中有23例(79%)患有腹膜后疾病,其中18例(62%)最初表现为晚期疾病。在接受原发性RPLDN的11例患者中,病理分期为6例中pN0(55%),3例中pN1(27%)和2例pN2(18%)。在接受初级RPLND治疗的7例临床I期患者中,1例腹膜后畸胎瘤和1例精原细胞瘤。在临床IIA期的4例患者中,2例患有畸胎瘤,1例患有胚胎癌。在中位随访时间为90.4个月时,有4例患者失去了随访,其他7例没有疾病(NED)的证据,且未复发。 18例接受化疗后RPLND的患者的病理结果显示纤维化在8例中,畸胎瘤在9例中,卵黄囊肿瘤在1例中。在最后的随访中,9例畸胎瘤的患者中有7例是NED,1例病死,1例死于未知原因。在8例纤维化患者中,有6例发生NED,有2例失去随访。生存期癌症患者在最后一次随访中接受了NED。结论:这些数据强调了纯睾丸畸胎瘤的转移潜力。低分期纯睾丸畸胎瘤患者中有很大一部分(45%)患有腹膜后疾病。此外,尽管在切除的腹膜后标本中已完全切除或组织学特征良好,但高比例(62%)的患者最初表现为晚期疾病,并显示出相当大的复发风险。

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