| Literature DB >> 32335819 |
John Lennon Silva Cunha1, Carla Isabelly Rodrigues-Fernandes1, Ciro Dantas Soares1, Celeste Sánchez-Romero1,2, Pablo Agustin Vargas1, Cleverson Luciano Trento3, Bruno Augusto Benevenuto de Andrade4, Sílvia Ferreira de Sousa5, Ricardo Luiz Cavalcanti de Albuquerque-Júnior6.
Abstract
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 α-SMA and HHF-35, and negativity for desmin, laminin, S-100, β-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.Entities:
Keywords: Jaws; Maxilla; Myofibroma; Pediatrics
Year: 2020 PMID: 32335819 PMCID: PMC8010050 DOI: 10.1007/s12105-020-01162-y
Source DB: PubMed Journal: Head Neck Pathol ISSN: 1936-055X