Department of Oral and Maxillofacial Medicine, School of Dentistry, Yasuj University of Medical Sciences, Yasuj, Iran.
Department of Oral and Maxillofacial Radiology, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, Iran.
Head Neck Pathol. 2021 Dec;15(4):1372-1376. doi: 10.1007/s12105-021-01298-5. Epub 2021 Feb 5.
Myxofibrosarcoma (MFS) is a fibroblastic soft tissue sarcoma that is extremely rare in the maxillofacial region. Due to its non-specific clinicoradiographic findings and challenging histopathological features, the diagnosis is difficult. Here, we present a case of MFS which was first diagnosed as nodular fasciitis. The initial examination of the incisional biopsy showed a benign-appearing proliferation of fibroblasts without features of malignancy. The patient returned with recurrence four months after surgical excision of the primary lesion. The second histologic study revealed a high-grade spindle cell sarcoma with myxoid features most compatible with MFS. Definitive diagnosis of MFS was confirmed by these histopathologic features and supportive immunohistochemical stains. Unfortunately, the patient died of disease 3 months later.
黏液纤维肉瘤(MFS)是一种极其罕见于颌面区域的纤维母细胞性软组织肉瘤。由于其非特异性的临床影像学表现和具有挑战性的组织病理学特征,诊断较为困难。在此,我们报告一例 MFS 病例,该病例最初被诊断为结节性筋膜炎。初次活检的检查显示良性表现的成纤维细胞增生,无恶性特征。患者在原发性病变切除术后 4 个月时因复发而返回。第二次组织学研究显示具有黏液样特征的高级别梭形细胞肉瘤,最符合 MFS 的表现。这些组织病理学特征和支持性免疫组织化学染色证实了 MFS 的明确诊断。不幸的是,患者在 3 个月后死于该疾病。