6533b7d4fe1ef96bd12634c3

RESEARCH PRODUCT

Clinicopathological study of oral focal mucinosis : a retrospective case series

Lélia-maria-guedes QueirozDenise-hélen-imaculada-pereira De OliveiraÉRicka Janine Dantas Da SilveiraAmanda-katarinny-goes GonzagaTiago-joão-da Silva FilhoMaria-luiza-diniz-de Sousa Lopes

subject

AdultMale0301 basic medicinePathologymedicine.medical_specialtyMucinosesAsymptomatic03 medical and health sciences0302 clinical medicineOral and maxillofacial pathologymedicineHumansGeneral DentistryAgedRetrospective StudiesOral Medicine and Pathologybusiness.industryResearchDiagnosis OralMiddle Aged:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseStaining030104 developmental biologyOtorhinolaryngologyCutaneous focal mucinosisUNESCO::CIENCIAS MÉDICAS030221 ophthalmology & optometryEtiologyImmunohistochemistryFemaleSurgerymedicine.symptomDifferential diagnosisMouth DiseasesMyxoid cystbusiness

description

Background Oral focal mucinosis (OFM) is a rare soft tissue lesion of unknown etiology that exhibits tumor-like growth. It is considered the oral counterpart of cutaneous focal mucinosis or cutaneous myxoid cyst. This is a retrospective study of oral OFM diagnosed over a period of 42 years at an oral pathology service. Material and Methods Clinical, histopathological and immunohistochemical data were analyzed. Alcian blue staining and S-100 immunohistochemistry were performed. Results Eleven cases were retrieved (4:1 female-to-male ratio). The mean age was 44 years. The gingiva was the most affected site. The main clinical presentation was sessile or pedunculated lesions of fibrous or hyperplasic appearance, most of them asymptomatic. Positive Alcian blue staining and absence of S-100 protein were observed in all specimens, which supported the histological diagnosis of OFM. Surgical excision was the treatment of choice. Conclusions Although rare, this study supports the inclusion of OFM in the differential diagnosis of intraoral myxoid lesions. Key words:Oral focal mucinosis, myxomatous lesion, connective tissue diseases, diagnosis.

10.4317/medoral.22291http://hdl.handle.net/10550/68041