Embryonal paratesticular rhabdomyosarcoma: A case report and a literature revue

被引：1
|
作者：
Ghorbal, L. [1 ]
Abid, W. [1 ]
Elloumi, F. [1 ]
Sallemi, T. [2 ]
Frikha, M. [3 ]
Daoud, J. [1 ]
机构：
[1] Univ Sfax, CHU Habib Bourguiba, Serv Radiotherapie Carcinol, Sfax 3027, Tunisia
[2] Univ Sfax, CHU Habib Bourguiba, Serv Anatomopathol, Sfax 3027, Tunisia
[3] Univ Sfax, CHU Habib Bourguiba, Serv Carcinol Med, Sfax 3027, Tunisia
来源：
CANCER RADIOTHERAPIE | 2015年 / 19卷 / 05期
关键词：
Rhabdomyosarcoma; Paratesticular; Treatment; PET;
D O I：
10.1016/j.canrad.2015.05.002
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
Paratesticular rhabdomyosarcoma is a rare tumor. Multimodality treatment should involve surgery, radiotherapy and chemotherapy, which are indicated according to risk groups. Risk group stratification depends on pretreatment staging and definitive histology. Patients older than 10 years or those with suspected lymph nodes on imaging have higher incidence of lymph node involvement. Prognosis is excellent for localized tumors, survival rates exceed 90%. We report a case of embryonal paratesticular rhabdomyosarcoma treated in our institution. (C) 2015 Societe francaise de radiotherapie oncologique (SFRO). Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码：334 / 336
页数：3
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