1. A solitary myofibroma in the mandibular region: Case report.
- Author
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Martínez-Gámez, J, Vázquez-Zúñiga, U, Pérez-Cornejo, N, Ramos-Baena, JD, Juárez, KM Avelar, Villanueva-Sánchez, FG, Sagrero, L, Silva-Suárez, R, and Cruz-Monroy, EA
- Abstract
Solitary myofibroma (SM) is a proliferation of myofibroblasts that primarily develops in children, with a predilection for the head and neck, being uncommon in the jaws and mouth, where clinically it has been described as a variable-sized nodule and imagenologically as a unilocular radiolucent lesion with well-defined borders, with or without erosion of the mandible. An 18-year-old female patient went to the Maxillofacial Surgery Department of the General Hospital of León with symptomatic tissue growth of approximately 6 cm in the left mandibular body. A hypodense, well-defined lesion was identified on tomography, and an excisional biopsy was performed. The histopathological study was carried out at the histopathological diagnosis service of ENES Unidad León, as well as an immunohistochemical panel and histochemical stains, determining the diagnosis of SM. The presence of SM in the mandible is rare, as evidenced by limited case reports and is even unusual in adults. Its clinical presentation can vary, and its histopathological appearance is very similar to other spindle cell lesions, which is why the similarities and differences between related lesions are discussed. MF represents a diagnostic challenge and, although rare, should be considered as a differential diagnosis of benign and malignant spindle cell mesenchymal proliferations. The diagnosis of these types of lesions should be based on histomorphology, with the use of immunohistochemistry and histochemistry being important to achieve their correct identification by exclusion and to implement appropriate management. [ABSTRACT FROM AUTHOR]
- Published
- 2025
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