Mostrar el registro sencillo del ítem
dc.contributor.author | Sanchez-Romero, Celeste | |
dc.contributor.author | Bonan, Paulo Rogerio Ferreti | |
dc.contributor.author | Pires, Fabio Ramoa | |
dc.contributor.author | Oliveira Silva-Junior, Geraldo | |
dc.contributor.author | Delgado Azanero, Wilson | |
dc.contributor.author | de Almeida, Oslei Paes | |
dc.contributor.author | da Cruz Perez, Danyel Elias | |
dc.date.accessioned | 2019-07-04T17:00:17Z | |
dc.date.available | 2019-07-04T17:00:17Z | |
dc.date.issued | 2019 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12866/6842 | |
dc.description.abstract | Objective. To present 4 new cases of oral leiomyomatous hamartomas (OLH), describing its clinical, microscopical, and immunohistochemical features, and a literature review. Methods. The OLH cases were retrieved from the files of 2 Brazilian and 1 Peruvian oral pathology services. Clinical data were obtained from the pathology reports. Microscopical features were reviewed, and immunohistochemical reactions were performed. A review of the English-language literature about OLH was done. Results. The sample was composed of 3 females (4-, 10-, and 15-year-old) and 1 male (3-year-old). Three cases affected the dorsum of the tongue and one the incisive papilla, and all presented sessile or pedunculated smooth nodules. Microscopically, the lesions were composed of varying-size fascicles of smooth muscle fibers in a fibrous connective tissue background. Immunohistochemistry revealed positivity of the smooth muscle bundles for myogenic markers. The English-language literature review revealed 38 OLH cases reported, most were congenital or diagnosed up to 5 years old. The main locations were tongue and anterior maxilla. Conclusions. Although OLH is a rare lesion, it must be considered in the differential diagnosis of midline tongue or maxillary masses in newborns, infants, and youngsters. | en_US |
dc.language.iso | eng | |
dc.publisher | SAGE Publications | |
dc.relation.ispartofseries | International Journal of Surgical Pathology | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es | |
dc.subject | adolescent | en_US |
dc.subject | Brazilian | en_US |
dc.subject | child | en_US |
dc.subject | clinical article | en_US |
dc.subject | clinical feature | en_US |
dc.subject | English (language) | en_US |
dc.subject | female | en_US |
dc.subject | hamartoma | en_US |
dc.subject | human | en_US |
dc.subject | immunohistochemistry | en_US |
dc.subject | leiomyoma | en_US |
dc.subject | leiomyomatous | en_US |
dc.subject | male | en_US |
dc.subject | mouth tumor | en_US |
dc.subject | oral | en_US |
dc.subject | oral leiomyomatous hamartoma | en_US |
dc.subject | Peruvian | en_US |
dc.subject | preschool child | en_US |
dc.subject | priority journal | en_US |
dc.subject | Review | en_US |
dc.subject | school child | en_US |
dc.subject | smooth muscle cell | en_US |
dc.title | Leiomyomatous Hamartomas of the Oral Cavity: Clinicopathological and Immunohistochemical Features of 4 Cases and Literature Review. | en_US |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | https://doi.org/10.1177/1066896919843337 | |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.01.09 | |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.02.11 | |
dc.relation.issn | 1940-2465 |
Ficheros | Tamaño | Formato | Ver |
---|---|---|---|
No hay ficheros asociados a este ítem. |