Demarosi Frederica, Bay Alessandro, Moneghini Laura, Carrassi Antonio
Unit of Oral Pathology and Medicine, Department of Medicine, Surgery and Dentistry, University of Milan, Milano, Italy.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009 Aug;108(2):248-54. doi: 10.1016/j.tripleo.2009.03.031.
Two cases of low-grade myofibroblastic sarcoma (LGMS) are presented: one of lateral tongue, the other of lower buccal vestibule. LGMS represents a distinct atypical myofibroblastic tumor that occurs in several sites, primarily within the head and neck regions. A painless, enlarging mass is the most common clinical presentation, but a definitive diagnosis requires both histopathological and immunohistochemical analyses. Histologically, LGMS commonly presents as a cellular lesion composed of spindle-shaped tumor cells arranged primarily in fascicles with a diffusely infiltrative pattern. Immunohistochemically, LGMS shows positive staining for at least one myogenic marker, such as desmin, and muscle actin.
本文报告两例低级别肌成纤维细胞肉瘤(LGMS):一例位于舌外侧,另一例位于颊前庭下部。LGMS是一种独特的非典型肌成纤维细胞肿瘤,可发生于多个部位,主要位于头颈部区域。无痛性肿块增大是最常见的临床表现,但明确诊断需要组织病理学和免疫组织化学分析。在组织学上,LGMS通常表现为一种细胞性病变,由主要呈束状排列并具有弥漫性浸润模式的梭形肿瘤细胞组成。在免疫组织化学方面,LGMS对至少一种肌源性标志物(如结蛋白和肌动蛋白)呈阳性染色。