Lazim Ahmed, Amer Samir M, Eltawil Ghadir M, Laski Robert, Kuklani Riya
Pathology, Temple University Hospital, Philadelphia, USA.
Dentistry, Al Hokail Specialized Digital Polyclinics Academy, Muharraq, BHR.
Cureus. 2024 Jul 10;16(7):e64232. doi: 10.7759/cureus.64232. eCollection 2024 Jul.
Myofibroma (MF) is a benign neoplasm derived from myofibroblasts. While they are infrequent, these tumors are predominantly found in the pediatric group and seldom manifest as intraosseous mandibular tumors. Herein, we present a 9-year-old female with a radiolucent lesion in the left mandible associated with malposed left lower canine and 1st premolar teeth. Clinical examination revealed a slightly tender 5×4 cm firm mass resulting in an expansion of the buccal and lingual aspects of the mandible in the canine and first premolar region. An incisional biopsy revealed a benign tumor consisting of spindle cells organized in fascicles, alongside dispersed thin-walled blood vessels. Tumor cells tested positive for α-smooth muscle actin (SMA) and vimentin. Given these findings, a diagnosis of MF was established. To the best of our knowledge, only 45 cases of solitary MF of the mandible have been reported in the pediatric age group in the literature. We describe one additional case and provide a review of the literature.
肌纤维瘤(MF)是一种源自肌成纤维细胞的良性肿瘤。虽然它们并不常见,但这些肿瘤主要见于儿童群体,很少表现为下颌骨骨内肿瘤。在此,我们报告一名9岁女性,其左下颌骨有一透射性病变,伴有左下尖牙和第一前磨牙错位。临床检查发现一个稍压痛的5×4厘米实性肿块,导致下颌骨颊侧和舌侧在尖牙和第一前磨牙区域膨隆。切开活检显示为一个良性肿瘤,由呈束状排列的梭形细胞以及散在的薄壁血管组成。肿瘤细胞α-平滑肌肌动蛋白(SMA)和波形蛋白检测呈阳性。基于这些发现,确诊为MF。据我们所知,文献中仅报道了45例儿童年龄组下颌骨孤立性MF病例。我们描述了另外一例并对文献进行了综述。