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Solitary fibrous tumor of the tongue.
Siqueira, Juliana Mota; Heguedusch, Daniele; Aguiar, Emília Maria Gomes; Dos Santos, Anaeliza Figueiredo; Alves, Fabio Abreu; Nunes, Fabio Daumas.
Afiliación
  • Siqueira JM; Universidade de São Paulo (USP), Dental School, Department of Oral and Maxillofacial Pathology, São Paulo, SP, Brasil.
  • Heguedusch D; Universidade de São Paulo (USP), Dental School, Department of Oral and Maxillofacial Pathology, São Paulo, SP, Brasil.
  • Aguiar EMG; Universidade de São Paulo (USP), Dental School, Department of Oral and Maxillofacial Pathology, São Paulo, SP, Brasil.
  • Dos Santos AF; Universidade de São Paulo (USP), Dental School, Department of Oral and Maxillofacial Pathology, São Paulo, SP, Brasil.
  • Alves FA; Universidade de São Paulo (USP), Dental School, Stomatology Department, São Paulo, SP, Brasil.
  • Nunes FD; A.C. Camargo Cancer Center, Stomatology Department, São Paulo, SP, Brasil.
Autops Case Rep ; 12: e2021405, 2022.
Article en En | MEDLINE | ID: mdl-36426115
Solitary fibrous tumor (SFT) is a benign mesenchymal neoplasm originally described in pleura with a rare presentation in the oral cavity. Herein, we report a case of a 28-year-old male patient who presented an asymptomatic slow-growing mass in the anterior part of the tongue. Intraoral examination revealed a well-circumscribed mass covered by normal mucosa with a fibrous consistency. Due to non-specific clinical findings, the initial diagnostic hypotheses include benign submucosal neoplasms such as leiomyoma, neurofibroma, SFT, and others. An excisional biopsy was performed. Microscopically, the tumor was surrounded by a thick fibrous capsule; hypo and hypercellular areas were arranged in a storiform pattern with a stroma formed by collagen and abundant vascularization. Tumor cells showed immunopositivity for CD34 and STAT-6 and no expression of CD99, AML, S-100, and Ki-67. According to these findings, the diagnosis of SFT was established. After 24 months, the patient is asymptomatic and has no evidence of recurrence. Although oral involvement is rare, SFT should be included in the differential diagnosis of oral submucosal lesions.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Autops Case Rep Año: 2022 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Autops Case Rep Año: 2022 Tipo del documento: Article País de afiliación: Brasil
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