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

被引:12
作者
Jayasooriya, Primali Rukmal [1 ]
Athukorala, Chamara [2 ]
Attygalla, Manjula [3 ]
Mendis, Balapuwaduge Ranjit Rigobert Nihal [4 ,5 ]
Lombardi, Tommaso [4 ,5 ]
机构
[1] Univ Peradeniya, Fac Dent Sci, Dept Oral Pathol, Peradeniya 20400, Sri Lanka
[2] Base Hosp, Oral & Maxillofacial Surg Unit, Badulla 9000, Sri Lanka
[3] Univ Peradeniya, Fac Dent Sci, Dept Oral & Maxillofacial Surg, Peradeniya 20400, Sri Lanka
[4] Univ Hosp Geneva, Unit Oral Med & Oral Maxillofacial Pathol, Lab Oral & Maxillofacial Pathol, CH-1211 Geneva GE 4, Switzerland
[5] Univ Geneva, Fac Med, CH-1211 Geneva GE 4, Switzerland
关键词
low-grade myofibroblastic sarcoma; oral cavity; mandible; gingiva; malignancy; immunohistochemistry; MYOFIBROSARCOMA; HEAD; NECK;
D O I
10.3390/dermatopathology8010001
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
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.
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页码:1 / 9
页数:9
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