Aggressive Intraosseous Myofibroma of the Maxilla: Report of a Rare Case and Literature Review

被引:9
作者
Silva Cunha, John Lennon [1 ]
Rodrigues-Fernandes, Carla Isabelly [1 ]
Soares, Ciro Dantas [1 ]
Sanchez-Romero, Celeste [1 ,2 ]
Vargas, Pablo Agustin [1 ]
Trento, Cleverson Luciano [3 ]
Benevenuto de Andrade, Bruno Augusto [4 ]
de Sousa, Silvia Ferreira [5 ]
Cavalcanti de Albuquerque-Junior, Ricardo Luiz [6 ]
机构
[1] Univ Estadual Campinas, Piracicaba Dent Sch, Dept Oral Diag, Oral Pathol Sect,UNICAMP, Piracicaba, SP, Brazil
[2] Univ La Republ, Fac Dent, Mol Pathol Area, Montevideo, Uruguay
[3] Fed Univ Sergipe UFS, Dept Dent, Aracaju, SE, Brazil
[4] Fed Univ Rio de Janeiro UFRJ, Sch Dent, Dept Oral Diag & Pathol, Rio De Janeiro, RJ, Brazil
[5] Univ Fed Minas Gerais, Sch Dent, Dept Oral Surg & Pathol, Belo Horizonte, MG, Brazil
[6] Tiradentes Univ Unit, Inst Technol & Res, Lab Morphol & Expt Pathol, Ave Murilo Dantas 300, BR-49032490 Aracaju, SE, Brazil
关键词
Myofibroma; Jaws; Maxilla; Pediatrics; SOLITARY FIBROUS TUMOR; NODULAR FASCIITIS; MYOFIBROBLASTIC TUMORS; INFANTILE MYOFIBROMA; NAB2-STAT6; FUSION; PDGFRB MUTATIONS; GENE; DIAGNOSIS; IMMUNOHISTOCHEMISTRY; EXPRESSION;
D O I
10.1007/s12105-020-01162-y
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Myofibroma (MF) is a benign mesenchymal myofibroblast-derived tumor, which occurs most frequently in children, and rarely affects the maxilla. We reported a case of an aggressive intraosseous lesion found in the maxilla of a 9-year-old female child. Intraorally, the swelling extended from tooth 12 to 16, causing displacement of teeth 13, 14, and 15. Computed tomography revealed a large osteolytic lesion causing thinning and cortical erosion. Microscopically, the lesion showed a proliferation of spindle-shaped cells, with elongated nuclei and eosinophilic cytoplasm, arranged in interlaced fascicles. The immunohistochemical analysis revealed cytoplasmic positivity for alpha-SMA and HHF-35, and negativity for desmin, laminin, S-100, beta-catenin, and CD34. Ki-67 was positive in 8% of tumor cells. The diagnosis was MF. Herein, we describe an additional case of central MF arising in the maxilla, including clinical, imaging, microscopical, and immunohistochemical features, as well as a review of the literature.
引用
收藏
页码:303 / 310
页数:8
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