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Epithelioid hemangioma in the oral cavity: Report of a rare case

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Resumo:Abstract The epithelioid hemangioma (EH), also known as angiolymphoid hyperplasia with eosinophilia, is a benign, neoplastic vascular tumor rarely presented in the mouth. It is most frequent in young adult male patients. Clinically, it is characterized by papules or nodules, usually with a reddish-brown color, mimicking other vascular and non-vascular lesions. Histologically, the lesion is composed of well-formed round vessels with epithelioid endothelial cells, with a histiocytoid appearance, surrounded by an infiltrate of lymphocytes and eosinophils. Oral EH’s endothelial cells are commonly immunoreactive for CD34 and factor VIII antigen. Surgical excision is the most widely used form of treatment, and recurrences are uncommon. The aim of this study was to report a rare case of oral EH in a 52-year-old female patient.
Autores principais:Assis,Fabiana Nunes de
Outros Autores:Mattos,Natanael Henrique Ribeiro; Milani,Cintia Mussi
Assunto:Angiolymphoid hyperplasia with eosinofilia Hemangioma Oral mucosa
Ano:2022
País:Portugal
Tipo de documento:relatório
Tipo de acesso:acesso aberto
Instituição associada:Fundação para a Ciência e Tecnologia
Idioma:inglês
Origem:SciELO Portugal
Descrição
Resumo:Abstract The epithelioid hemangioma (EH), also known as angiolymphoid hyperplasia with eosinophilia, is a benign, neoplastic vascular tumor rarely presented in the mouth. It is most frequent in young adult male patients. Clinically, it is characterized by papules or nodules, usually with a reddish-brown color, mimicking other vascular and non-vascular lesions. Histologically, the lesion is composed of well-formed round vessels with epithelioid endothelial cells, with a histiocytoid appearance, surrounded by an infiltrate of lymphocytes and eosinophils. Oral EH’s endothelial cells are commonly immunoreactive for CD34 and factor VIII antigen. Surgical excision is the most widely used form of treatment, and recurrences are uncommon. The aim of this study was to report a rare case of oral EH in a 52-year-old female patient.

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