A rare benign tumor mimicking an inflammatory reactive lesion

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dc.creatorSara Ferreira dos Santos Costa
dc.creatorMaria Cassia Ferreira de Aguiar
dc.creatorPatrícia Carlos Caldeira
dc.date.accessioned2024-07-31T19:54:38Z
dc.date.accessioned2025-09-09T00:57:40Z
dc.date.available2024-07-31T19:54:38Z
dc.date.issued2017-08
dc.description.sponsorshipCNPq - Conselho Nacional de Desenvolvimento Científico e Tecnológico
dc.description.sponsorshipFAPEMIG - Fundação de Amparo à Pesquisa do Estado de Minas Gerais
dc.description.sponsorshipCAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
dc.format.mimetypepdf
dc.identifier.doihttps://doi.org/10.1016/j.oooo.2017.05.032
dc.identifier.issn2212-4411
dc.identifier.urihttps://hdl.handle.net/1843/72224
dc.languageeng
dc.publisherUniversidade Federal de Minas Gerais
dc.relation.ispartofOral Surgery Oral Medicine Oral Pathology Oral Radiology
dc.rightsAcesso Restrito
dc.subjectGranuloma, pyogenic
dc.subjectFibroma
dc.subjectNeoplasms
dc.subjectDiagnosis
dc.subjectEpithelium
dc.subject.othersoft tissue tumors Oral Surgery Oral Medicine Oral Pathology Oral Radiology
dc.subject.otherSupport: CAPES, FAPEMIG, CNPq acesso restrito A rare benign tumor mimicking an inflammatory reactive lesion data 30/07/2024 julho terça-feira ano d.c depois de Cristo horario 15 e 03
dc.titleA rare benign tumor mimicking an inflammatory reactive lesion
dc.typeArtigo de periódico
local.citation.epageE67
local.citation.issue2
local.citation.spageE67
local.citation.volume124 Oral Surgery Oral Medicine Oral Pathology Oral Radiology
local.description.resumoThe present case reports a rare benign tumor of a 30-year-old female patient presenting with a painless, erythematous, sessile, firm, localized swelling on the distal of the left mandibular pre molar of approximately 3 years’ duration. Covering mucosa was intact and there was no bone involvement. The initial clinical diagnosis was pyogenic granuloma. An excisional biopsy was performed and the histopathologic examination showed a mark edly cellular connective tissue intermixed with nests and strands of inactive-looking odontogenic epithelium. Deposition of a mineralized material resembling dentinoid was seen. The epithelial elements were positive for AE1/AE3 and CK14. The histopathologic and immunohistochemical features were consis tent with a diagnosis of peripheral odontogenic fibroma, epithe lium-rich type. No recurrence was found during a 4-month follow-up. Peripheral odontogenic fibroma is often misdiagnosed as a reactive lesion because of similar clinical features and, thus, a histopathologic examination is required for accurate definitive diagnosis.
local.identifier.orcidhttps://orcid.org/0000-0001-9273-376X
local.publisher.countryBrasil
local.publisher.departmentFAO - DEPARTAMENTO DE CLÍNICA
local.publisher.initialsUFMG
local.url.externahttps://www.oooojournal.net/article/S2212-4403(17)30325-5/fulltext

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