Department of Urology, Kobe Children’s Hospital, Kobe, Hyogo, Japan.
Int J Urol. 2010 Nov;17(11):956-9. doi: 10.1111/j.1442-2042.2010.02629.x.
Testicular tumors are rare in children. In addition, prepubertal testicular tumors (PTT) are fundamentally different from their postpubertal counterparts.We reviewed our 20-year experience with 40 cases to suggest an algorithm for the appropriate surgical approach for patients with PTT. All tumors ultrasonographically suspected of being benign were confirmed to be benign postoperatively. There was a significant difference between median preoperative a-fetoprotein (AFP) levels of infants with yolk sac tumor and teratoma. The majority of our cases were benign, with the most common histopathological subtype being teratoma, as recently reported. Testis-sparing surgery was carried out in five patients with teratoma and three patients with epidermoid cyst. Other than one patient with teratoma, none of the patients developed recurrence or testicular atrophy after testis-sparing surgery. When testis-sparing surgery is considered, our algorithm based on ultrasonographic findings and preoperative AFP levels might be helpful.
睾丸肿瘤在儿童中较为罕见。此外,青春期前睾丸肿瘤(PTT)与青春期后睾丸肿瘤在根本上有所不同。我们回顾了 20 年来治疗 40 例 PTT 患者的经验,提出了一种适用于此类患者的手术方法的算法。所有超声怀疑为良性的肿瘤术后均证实为良性。卵黄囊瘤和畸胎瘤患儿术前中位甲胎蛋白(AFP)水平有显著差异。与最近的报道一致,我们的大多数病例为良性,最常见的组织病理学亚型是畸胎瘤。对 5 例畸胎瘤和 3 例表皮样囊肿患者进行了保留睾丸手术。除 1 例畸胎瘤患者外,其余行保留睾丸手术后患者均未复发或出现睾丸萎缩。当考虑保留睾丸手术时,我们基于超声检查结果和术前 AFP 水平的算法可能会有所帮助。