首页> 外文期刊>Journal of the Chinese Medical Association: JCMA >Prepubertal testicular germ cell tumors: 25-year experience in Taipei Veterans General Hospital.
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Prepubertal testicular germ cell tumors: 25-year experience in Taipei Veterans General Hospital.

机译:青春期前睾丸生殖细胞肿瘤:在台北荣民总医院有25年的工作经验。

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BACKGROUND: Due to the rarity of testicular tumors in the prepubertal population, adequate information about their biological course is difficult to document well in a single institution. The purpose of this study was to focus on prepubertal males in an attempt to evaluate clinical features and optimal management among various testicular germ cell tumors with long-term follow-up. METHODS: We retrospectively reviewed the records of children younger than 12 years of age with primary testicular germ cell tumors between February 1981 and December 2005 at Taipei Veterans General Hospital. Thirty-four children were diagnosed with adequate clinical and pathologic data. The stage of the disease was determined according to the staging system used by the Children's Oncology Group. Mean follow-up time was 139 months (range, 2-283 months). RESULTS: All of the 34 prepubertal patients were diagnosed initially with a painless scrotal mass. The mean age of the patients at diagnosis ranged from 6 months to 84 months (mean, 20.5 months). All patients underwent radical orchiectomy as an initial treatment. Twenty-nine (85.3%) patients had yolk sac tumors, and 5 (14.7%) had mature teratomas. Of the 29 patients with yolk sac tumor, 26 (89.7%) were diagnosed as stage I, 1 (3.4%) as stage III, and 2 (7.0%) as stage IV. Five (19.2%) of the 26 stage I yolk sac tumors progressed to metastasis after radical orchiectomy, and all of these 5 patients later received chemotherapy. One patient initially with stage III yolk sac tumor and 2 patients with stage IV yolk sac tumor were also treated with chemotherapy. Eventually, 1 patient with stage IV yolk sac tumor died due to tumor progression; the remaining 28 patients with yolk sac tumor all survived without tumor relapse after appropriate treatment. In the 5 patients with teratomas, there was no tumor relapse after radical orchiectomy with a mean follow-up time of 139.1 months. The 5-year survival rates for yolk sac tumor and teratomas were 96.5% and 100%, respectively. CONCLUSION: The most common prepubertal malignant testicular tumor is yolk sac tumor, and the most common benign testicular tumor is teratoma. Children with testicular germ cell tumors have excellent long-term survival rates after appropriate treatment.
机译:背景:由于青春期前睾丸肿瘤的罕见性,很难在一个机构中很好地记录有关其生物学过程的足够信息。这项研究的目的是集中于青春期前男性,以期通过长期随访来评估各种睾丸生殖细胞肿瘤的临床特征和最佳治疗。方法:我们回顾性研究了1981年2月至2005年12月在台北荣民总医院进行的12岁以下原发性睾丸生殖细胞肿瘤儿童的记录。 34名儿童被诊断出具有足够的临床和病理数据。根据儿童肿瘤学小组使用的分期系统确定疾病的分期。平均随访时间为139个月(范围2-283个月)。结果:34例青春期前患者最初被诊断为无痛阴囊肿块。诊断时患者的平均年龄为6个月至84个月(平均20.5个月)。所有患者均接受根治性睾丸切除术作为初始治疗。 29名(85.3%)患者患有卵黄囊瘤,而5名(14.7%)患者患有成熟的畸胎瘤。在29例卵黄囊瘤患者中,诊断为I期26例(89.7%),诊断为III期1例(3.4%),诊断为IV期2例(7.0%)。根治性睾丸切除术后26例I期卵黄囊肿瘤中有5例(19.2%)进展为转移,这5例患者全部接受了化疗。最初患有III期卵黄囊肿瘤的一名患者和两名患有IV期卵黄囊肿瘤的患者也接受了化疗。最终,有1例IV期卵黄囊肿瘤患者因肿瘤进展而死亡。其余28例卵黄囊瘤患者经适当治疗后均存活,无肿瘤复发。在5例畸胎瘤患者中,根治性睾丸切除术后无肿瘤复发,平均随访时间为139.1个月。卵黄囊瘤和畸胎瘤的5年生存率分别为96.5%和100%。结论:青春期前最常见的睾丸恶性肿瘤是卵黄囊肿瘤,最常见的良性睾丸良性肿瘤是畸胎瘤。患有睾丸生殖细胞肿瘤的儿童经过适当治疗后具有极好的长期存活率。

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