Lahbali Othmane, Azami Amine, Tbouda Mohammed, Elyamine Adil, Zouaidia Fouad, Mahassini Najat
Service d'Anatomie Pathologique, Centre Hospitalier Universitaire Ibn Sina, Rabat, Maroc.
Service d'Histologie, Centre Hospitalier Universitaire Ibn Sina, Rabat, Faculté de Médecine de Casablanca, Maroc.
Pan Afr Med J. 2017 Feb 20;26:69. doi: 10.11604/pamj.2017.26.69.11339. eCollection 2017.
Mammary-type myofibroblastoma (MTMF) is a rare benign mesenchymal tumor, initially detected in the breast. Its diagnosis is based on a spectrum of clinical, radiological and possibly histological parameters. We here report the rare case of a 50 year old male patient with mammary-type myofibroblastoma located in the axillary region. The peculiarity of our case lies in the presence of numerous mitoses and this was rarely described in the literature. The aim of our case study was to raise the problem of differential diagnosis of this rare tumor.
乳腺型肌纤维母细胞瘤（MTMF）是一种罕见的良性间叶组织肿瘤，最初在乳腺中被发现。其诊断基于一系列临床、放射学以及可能的组织学参数。我们在此报告一例罕见病例，一名50岁男性患者，其乳腺型肌纤维母细胞瘤位于腋窝区域。我们病例的独特之处在于存在大量有丝分裂，而这在文献中鲜有描述。我们病例研究的目的是提出这种罕见肿瘤的鉴别诊断问题。
