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Solitary fibrous tumor of the tongue
Siqueira, Juliana Mota; Heguedusch, Daniele; Aguiar, Emília Maria Gomes; Santos, Anaeliza Figueiredo dos; Alves, Fabio Abreu; Nunes, Fabio Daumas.
Afiliación
  • Siqueira, Juliana Mota; Universidade de São Paulo. Dental School, Department of Oral and Maxillofacial Pathology. São Paulo. BR
  • Heguedusch, Daniele; Universidade de São Paulo. Dental School, Department of Oral and Maxillofacial Pathology. São Paulo. BR
  • Aguiar, Emília Maria Gomes; Universidade de São Paulo. Dental School, Department of Oral and Maxillofacial Pathology. São Paulo. BR
  • Santos, Anaeliza Figueiredo dos; Universidade de São Paulo. Dental School, Department of Oral and Maxillofacial Pathology. São Paulo. BR
  • Alves, Fabio Abreu; Universidade de São Paulo. Dental School, Stomatology Department. São Paulo. BR
  • Nunes, Fabio Daumas; Universidade de São Paulo. Dental School, Department of Oral and Maxillofacial Pathology. São Paulo. BR
Autops. Case Rep ; 12: e2021405, 2022. graf
Article en En | LILACS-Express | LILACS | ID: biblio-1403555
Biblioteca responsable: BR1.1
ABSTRACT
ABSTRACT 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: LILACS Idioma: En Revista: Autops. Case Rep Asunto de la revista: Anatomia / Patologia Cl¡nica / Patologia Legal Año: 2022 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Base de datos: LILACS Idioma: En Revista: Autops. Case Rep Asunto de la revista: Anatomia / Patologia Cl¡nica / Patologia Legal Año: 2022 Tipo del documento: Article País de afiliación: Brasil
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