Department of Urology and Oncology, Children's Hospital, Zhejiang University School of Medicine, 57# Zhu Gan Xiang, Hangzhou, 310003, China.
J Pediatr Surg. 2012 Aug;47(8):1576-80. doi: 10.1016/j.jpedsurg.2011.11.005.
Prepubertal testicular tumors are rare and fundamentally distinct from adult testicular tumors. We reviewed our 11-year experience in a single medical center of China.
This study reports the clinical characteristics, histopathologic diagnosis, treatment methods, and outcome in a series of 63 prepubertal boys who were treated between 1997 and 2008.
A total of 63 primary prepubertal testicular and paratesticular tumors were identified. The median age at presentation was 11 months. Of these tumors, 27 (42.9%) were mature teratomas, 5 (7.9%) were immature teratomas, 21 (33.3%) were yolk sac tumors, 4 (6.3%) were epidermoid cyst, 2 (3.2%) were Leydig cell tumors, 1 (1.6%) was a mixed malignant germ cell tumor, and 3 (4.8%) were paratesticular tumors. The most common clinical presentation (95.2%) was a painless scrotal mass or swelling. Forty-eight tumors were treated with radical inguinal orchiectomy, and 15, with a testis-sparing procedure. Follow-up was available in 59 cases, range from 4 to 128 months (median, 50 months). One patient with yolk sac tumor had recurrence and progression to metastasis at the end of 4 months after surgery. Other patients were disease free at last follow-up.
Most of the prepubertal testicular lesions were benign, and the most common histologic subtype was teratoma. Our experience with testis-sparing procedures supports the current trends that less invasive treatment should be performed for benign lesions. This study confirms the excellent cure rates obtained in children with prepubertal testicular tumors.
青春期前睾丸肿瘤罕见,与成人睾丸肿瘤有根本区别。我们回顾了 11 年来在我们中心的诊治经验。
本研究报告了 1997 年至 2008 年间在一家中国医学中心接受治疗的 63 例青春期前男孩的临床特征、组织病理学诊断、治疗方法和结果。
共发现 63 例原发性青春期前睾丸和附睾丸肿瘤。中位发病年龄为 11 个月。其中 27 例(42.9%)为成熟畸胎瘤,5 例(7.9%)为未成熟畸胎瘤,21 例(33.3%)为卵黄囊瘤,4 例(6.3%)为表皮样囊肿,2 例(3.2%)为间质细胞瘤,1 例(1.6%)为混合性恶性生殖细胞瘤,3 例(4.8%)为附睾丸肿瘤。最常见的临床表现(95.2%)是无痛性阴囊肿块或肿胀。48 例肿瘤行根治性腹股沟睾丸切除术,15 例行保留睾丸手术。59 例可获得随访,随访时间为 4 至 128 个月(中位随访时间 50 个月)。1 例卵黄囊瘤患者在手术后 4 个月时复发并进展为转移。其他患者在最后一次随访时均无疾病。
大多数青春期前睾丸病变为良性,最常见的组织学类型为畸胎瘤。我们对保留睾丸手术的经验支持目前的趋势,即对于良性病变应采用更微创的治疗方法。本研究证实了儿童青春期前睾丸肿瘤获得良好治愈率的事实。