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睾丸卵黄囊瘤和成熟畸胎瘤:一名婴儿双侧同时发生

Testicular Yolk Sac Tumor and Mature Teratoma: Synchronous Bilateral Occurrence in an Infant.

作者信息

Dong Shuo, Zhao Linsheng, Pei Guanghua, Zhang Yanjun, Wang Shicheng

机构信息

Department of Ultrasound, Tianjin Children's Hospital, Tianjin, China.

Department of Pathology, Tianjin Children's Hospital, Tianjin, China.

出版信息

Urology. 2018 Jul;117:142-144. doi: 10.1016/j.urology.2018.03.025. Epub 2018 Mar 30.

Abstract

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.

摘要

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。

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