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Ossifying Fibromyxoid Tumor of the Retromolar Trigone: A Case Report and Systematic Review of the Literature.
Titsinides, Savvas; Nikitakis, Nikolaos G; Tasoulas, Jason; Daskalopoulos, Argyriοs; Goutzanis, Lampros; Sklavounou, Alexandra.
Afiliación
  • Titsinides S; 1 Department of Oral Medicine and Pathology, School of Dentistry, National and Kapodistrian University of Athens, Greece.
  • Nikitakis NG; 1 Department of Oral Medicine and Pathology, School of Dentistry, National and Kapodistrian University of Athens, Greece.
  • Tasoulas J; 1 Department of Oral Medicine and Pathology, School of Dentistry, National and Kapodistrian University of Athens, Greece.
  • Daskalopoulos A; 1 Department of Oral Medicine and Pathology, School of Dentistry, National and Kapodistrian University of Athens, Greece.
  • Goutzanis L; 2 Department of Oral and Maxillofacial Surgery, School of Dentistry, National and Kapodistrian University of Athens, Greece.
  • Sklavounou A; 1 Department of Oral Medicine and Pathology, School of Dentistry, National and Kapodistrian University of Athens, Greece.
Int J Surg Pathol ; 25(6): 526-532, 2017 Sep.
Article en En | MEDLINE | ID: mdl-28436288
ABSTRACT
Ossifying fibromyxoid tumor (OFMT) is a mesenchymal neoplasm of uncertain lineage and intermediate biologic behavior. Involvement of the head and neck area is infrequent (10% to 15%) and intraoral presentation is very rare. An OFMT developing in the retromolar trigone of a 13-year-old male is presented, along with a comprehensive review of oral OFMT cases. Among 12 oral OFMTs (including the present case), most patients were male (72.7%), with a mean age of 30.3 (13-67) years. The tumors generally appeared as painless masses of firm or hard consistency (mean diameter 27.7 mm), most commonly located in the soft tissues of the mandible (50%). Common microscopic features included ossification, lack of atypia or high mitotic activity, and immunohistochemical positivity for S100 (5/7), vimentin (6/6), GFAP (3/6), and SMA (2/6). Recurrence was reported only in one case. Further characterization of this rare entity is needed to increase our understanding of its distinct clinical and histopathologic features.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Boca / Fibroma Osificante Tipo de estudio: Systematic_reviews Límite: Adolescent / Humans / Male Idioma: En Revista: Int J Surg Pathol Asunto de la revista: PATOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Grecia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Boca / Fibroma Osificante Tipo de estudio: Systematic_reviews Límite: Adolescent / Humans / Male Idioma: En Revista: Int J Surg Pathol Asunto de la revista: PATOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Grecia