Azami Mohamed Amine, Alami Iliass El, Bourhafour Imane, Belhabib Salwa, Oukabli Mohamed, Albouzidi Abderrahmane
Service d'Anatomie Pathologique, Hôpital Militaire d'Instruction Mohamed V de Rabat, Maroc.
Service d'Oncologie Médicale, Hôpital Militaire d'Instruction Mohamed V de Rabat, Maroc.
Pan Afr Med J. 2017 May 8;27:14. doi: 10.11604/pamj.2017.27.14.8977. eCollection 2017.
Gliosarcoma is a very rare brain tumor accounting for 1.8 -8% of all glial tumors. It has been classified by the World Health Organization as a variant of glioblastoma. It is a tumor with double glial and sarcomatous component. Patient's clinical picture is polymorphic, imaging data are evocative, diagnosis is based on histology. Treatment is always surgical. Prognosis is closely linked to the quality of resection. We here report two clinical cases with the aim of assessing the diagnostic, therapeutic and prognostic features of this rare entity.
胶质肉瘤是一种非常罕见的脑肿瘤,占所有胶质瘤的1.8%-8%。世界卫生组织已将其归类为胶质母细胞瘤的一种变体。它是一种具有双胶质和肉瘤成分的肿瘤。患者的临床表现具有多态性,影像学数据具有提示性,诊断基于组织学。治疗总是采取手术方式。预后与切除质量密切相关。我们在此报告两例临床病例,旨在评估这种罕见疾病的诊断、治疗和预后特征。