Ahsaini Mustapha, Mellouki Adil, Ouattar Khalid, Azelmad Hamid, Mellas Soufiane, Ammari Jalaleddine, Tazi Mohammed Fadl, Fassi Mohammed Jamal, Farih Moulay Hassan
Service d'Urologie, CHU Hassan II de Fès, Fès, Maroc.
Pan Afr Med J. 2018 Jun 11;30:107. doi: 10.11604/pamj.2018.30.107.15772. eCollection 2018.
Embryonic paratesticular rhabdomyosarcoma is a rare mesenchymal tumor constituting a diagnostic and therapeutic emergency. Localized forms have a favorable prognosis. Multimodal treatment is the gold standard and it is based on surgery, multidrug chemotherapy and radiotherapy, with excellent overall survival rate. We here report the case of a 17-year old patient treated in our Department for embryonic fusiform cell paratesticular rhabdomyosarcoma causing clinical confusion. This study aims to highlight the specific features of this disease.
胚胎型睾丸旁横纹肌肉瘤是一种罕见的间叶组织肿瘤,构成诊断和治疗上的紧急情况。局限性病例预后良好。多模式治疗是金标准,其基于手术、多药化疗和放疗,总体生存率极佳。我们在此报告一名17岁患者的病例,该患者在我们科室接受治疗,患有胚胎型梭形细胞睾丸旁横纹肌肉瘤,引发了临床诊断上的困惑。本研究旨在突出该疾病的具体特征。