Dong Shuo, Zhao Linsheng, Pei Guanghua, Zhang Yanjun, Wang Shicheng
Department of Ultrasound, Tianjin Children's Hospital, Tianjin, China.
Department of Pathology, Tianjin Children's Hospital, Tianjin, China.
Urology. 2018 Jul;117:142-144. doi: 10.1016/j.urology.2018.03.025. Epub 2018 Mar 30.
Yolk sac tumor (YST) is a rare malignancy typically occurring in children. However, bilateral testicular YSTs are a quite rare situation, which can occur metachronously or synchronously with same histologic type, as well as different histology. We present a case of synchronous YST of the left testis and mature teratoma of the right in a 7-month-old infant treated with testis-sparing surgery at right testis and high radical orchiectomy at left. By follow-up of 28th month, no atrophy, or residual tumor in right testis and no recurrence or evidence of disease in left scrotum was found.
卵黄囊瘤(YST)是一种罕见的恶性肿瘤,通常发生于儿童。然而,双侧睾丸卵黄囊瘤是一种非常罕见的情况,可同时或异时发生,组织学类型相同或不同。我们报告一例7个月大婴儿,其左侧睾丸为同步卵黄囊瘤,右侧为成熟畸胎瘤,对右侧睾丸行保留睾丸手术,对左侧睾丸行根治性高位睾丸切除术。随访至第28个月时,右侧睾丸未发现萎缩或残留肿瘤,左侧阴囊未发现复发或疾病迹象。