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口腔低度恶性肌纤维母细胞肉瘤:三例报告并阐述儿童中的一种新出现疾病

Low-Grade Myofibroblastic Sarcoma of the Oral Cavity: A Report of Three Cases Illustrating an Emerging Disease in Children.

作者信息

Jayasooriya Primali Rukmal, Athukorala Chamara, Attygalla Manjula, Mendis Balapuwaduge Ranjit Rigobert Nihal, Lombardi Tommaso

机构信息

Department of Oral Pathology, Faculty of Dental Sciences, University of Peradeniya, Peradeniya 20400, Sri Lanka.

Oral and Maxillofacial Surgery Unit, Base Hospital, Badulla 9000, Sri Lanka.

出版信息

Dermatopathology (Basel). 2021 Jan 1;8(1):1-9. doi: 10.3390/dermatopathology8010001.

Abstract

Low-grade myofibroblastic sarcoma (LGMS) is a mesenchymal tumor of myofibroblasts that occurs more frequently in adults. A series of three cases is presented to illustrate that LGMS may also occur within the oral cavity in children and adolescents. The first case (Case 1) occurred intra-osseously in the mandible, while the remaining two presented as gingival swellings and were purely restricted to soft tissue (cases 2 and 3). The intra-osseous lesion arose in a 7-year-old girl, whereas the gingival lesions were observed in a 12-year-old girl (Case 2) and a 13-year-old boy (Case 3). Histopathologically, all cases were composed of spindle shaped cells arranged into long fascicles showing mild to moderate degree of nuclear atypia. Ki-67 (MIB-1) proliferation activity was relatively low, amounting to 3-5% in all cases. Immunohistochemically, all cases showed smooth muscle actin (SMA) positivity in spindle cells, while desmin, beta catenin, cytokeratin, and CD34 were negative, resulting in a diagnosis of LGMS. In conclusion, current series of three cases of LGMSs that occurred in the oral cavity in a child and two adolescent patients is presented to highlight an emerging disease that requires additional data for further characterization.

摘要

低度恶性肌成纤维细胞肉瘤(LGMS)是一种肌成纤维细胞的间叶性肿瘤,在成人中更为常见。本文报告三例病例,以说明LGMS也可能发生于儿童和青少年的口腔内。第一例(病例1)发生于下颌骨的骨内,而其余两例表现为牙龈肿胀,且仅局限于软组织(病例2和病例3)。骨内病变发生在一名7岁女孩身上,而牙龈病变分别见于一名12岁女孩(病例2)和一名13岁男孩(病例3)。组织病理学上,所有病例均由梭形细胞组成,排列成束状,核异型性为轻度至中度。Ki-67(MIB-1)增殖活性相对较低,所有病例中均为3%-5%。免疫组织化学检查显示,所有病例的梭形细胞中平滑肌肌动蛋白(SMA)呈阳性,而结蛋白、β-连环蛋白、细胞角蛋白和CD34均为阴性,最终诊断为LGMS。总之,本文报告了三例发生于儿童和两名青少年患者口腔内的LGMS病例,以强调这一新兴疾病,需要更多数据以进一步明确其特征。

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