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青春期前睾丸生殖细胞肿瘤:台北荣民总医院25年经验

Prepubertal testicular germ cell tumors: 25-year experience in Taipei Veterans General Hospital.

作者信息

Chen Yin-Shen, Kuo Junne-Yih, Chin Tai-Wai, Wei Chou-Fu, Chen Kuang-Kuo, Lin Alex T L, Chang Luke S

机构信息

Division of Urology, Department of Surgery, Taipei Veterans General Hospital, and Department of Urology, National Yang-Ming University School of Medicine, Taipei, Taiwan, ROC.

出版信息

J Chin Med Assoc. 2008 Jul;71(7):357-61. doi: 10.1016/S1726-4901(08)70139-4.

Abstract

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.

摘要

背景

由于青春期前人群睾丸肿瘤罕见,在单一机构中很难充分记录其生物学病程。本研究旨在聚焦青春期前男性,试图评估各种睾丸生殖细胞肿瘤的临床特征及最佳治疗方法,并进行长期随访。

方法

我们回顾性分析了1981年2月至2005年12月在台北荣民总医院诊断为原发性睾丸生殖细胞肿瘤的12岁以下儿童的病历。34名儿童有充分的临床和病理资料。根据儿童肿瘤协作组使用的分期系统确定疾病分期。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均诊断为无痛性阴囊肿块。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例(85.3%)患者为卵黄囊瘤,5例(14.7%)为成熟畸胎瘤。在29例卵黄囊瘤患者中,26例(89.7%)诊断为I期,1例(3.4%)为III期,2例(7.0%)为IV期。26例I期卵黄囊瘤患者中有5例(19.2%)在根治性睾丸切除术后发生转移,这5例患者随后均接受了化疗。1例最初为III期卵黄囊瘤患者和2例IV期卵黄囊瘤患者也接受了化疗。最终,1例IV期卵黄囊瘤患者因肿瘤进展死亡;其余28例卵黄囊瘤患者经适当治疗后均存活且无肿瘤复发。5例畸胎瘤患者在根治性睾丸切除术后平均随访139.1个月无肿瘤复发。卵黄囊瘤和畸胎瘤的5年生存率分别为96.5%和100%。

结论

青春期前最常见的恶性睾丸肿瘤是卵黄囊瘤,最常见的良性睾丸肿瘤是畸胎瘤。睾丸生殖细胞肿瘤患儿经适当治疗后长期生存率良好。

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