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12 岁男孩的睾丸旁胎儿型横纹肌肉瘤:病例报告及文献复习。

Paratesticular fetal-type rhabdomyoma in a 12-year-old boy: a case report and literature review.

机构信息

Department of Dermatology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, China.

出版信息

Urology. 2013 Nov;82(5):1150-2. doi: 10.1016/j.urology.2013.04.029. Epub 2013 Jun 14.

DOI:10.1016/j.urology.2013.04.029
PMID:23768526
Abstract

Fetal rhabdomyoma (F-RM) is a very rare tumor that usually occurs in the head and neck. Paratesticular F-RM in children is extremely rare. In this article, we report the case of a 12-year-old boy diagnosed with paratesticular F-RM. The patient was well, with no local recurrence or metastasis 5 years after excision of the tumor. To our knowledge, this is the first case of F-RM reported in an adolescent. We also reviewed the literature and compared our patient with the 11 previously reported patients with F-RM.

摘要

胎儿横纹肌瘤(F-RM)是一种非常罕见的肿瘤,通常发生在头颈部。儿童的睾丸旁 F-RM 极为罕见。本文报道了 1 例 12 岁男性睾丸旁 F-RM 病例。患者术后 5 年,局部无复发及转移,恢复良好。据我们所知,这是首例青少年 F-RM 报道。同时,我们复习了相关文献,并将我们的患者与之前报道的 11 例 F-RM 患者进行了比较。

相似文献

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Paratesticular fetal-type rhabdomyoma in a 12-year-old boy: a case report and literature review.12 岁男孩的睾丸旁胎儿型横纹肌肉瘤:病例报告及文献复习。
Urology. 2013 Nov;82(5):1150-2. doi: 10.1016/j.urology.2013.04.029. Epub 2013 Jun 14.
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