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 |
|