Non-familial Cherubism – Report of a case
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Dental Science |
Texto Completo: | https://ojs.ict.unesp.br/index.php/cob/article/view/1137 |
Resumo: | Introduction: The Cherubism is a rare disease that affects the middle and lower third of the face in individuals at the time of childhood. It is a rare hereditary benign bone disease with an autosomal dominant inheritance. The familial distribution may affect different generations and isolated non-familial cases have also been reported in literature. Lesions appear as cystic multilocular radiolucencies, histologically, resembles central giant cell granluloma and hyperparathyroidism brown tumor with numerous randomly distributed multinucleated giant cells and vascular spaces within a fibrous connective tissue stroma. Objectives: The aim of this study is to report the importance of the diagnosis of this pathology and the variety of treatments available in the literature, thus guiding to an individualized treatment. Case Report: Caucasian 8 years-old female, in good general condition, was referred to Service of Oral and Maxillofacial Surgery of Erasto Gaertner Hospital (EGH), Curitiba – PR, Brazil, complaining of bilateral swelling of the maxilla and mandible since 4 years-old. Apparently, the girl is the first one who developed the genetic pathology in at least 4 generation of her family. After biopsy, cherubism diagnosis was confirmed and the treatment of choice was periodic monitoring. Discussion: Cherubism studies with long-term follow-up with clinical and radiographic documentation indicate that the spontaneous resolution of bone lesions is rare. Treatment of cherubism is controversial and various modalities have been reported as the use of calcitonin, osseous plasty surgery, curettage, orthognathic surgery, liposuction and palliative treatments. |
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Non-familial Cherubism – Report of a caseIntroduction: The Cherubism is a rare disease that affects the middle and lower third of the face in individuals at the time of childhood. It is a rare hereditary benign bone disease with an autosomal dominant inheritance. The familial distribution may affect different generations and isolated non-familial cases have also been reported in literature. Lesions appear as cystic multilocular radiolucencies, histologically, resembles central giant cell granluloma and hyperparathyroidism brown tumor with numerous randomly distributed multinucleated giant cells and vascular spaces within a fibrous connective tissue stroma. Objectives: The aim of this study is to report the importance of the diagnosis of this pathology and the variety of treatments available in the literature, thus guiding to an individualized treatment. Case Report: Caucasian 8 years-old female, in good general condition, was referred to Service of Oral and Maxillofacial Surgery of Erasto Gaertner Hospital (EGH), Curitiba – PR, Brazil, complaining of bilateral swelling of the maxilla and mandible since 4 years-old. Apparently, the girl is the first one who developed the genetic pathology in at least 4 generation of her family. After biopsy, cherubism diagnosis was confirmed and the treatment of choice was periodic monitoring. Discussion: Cherubism studies with long-term follow-up with clinical and radiographic documentation indicate that the spontaneous resolution of bone lesions is rare. Treatment of cherubism is controversial and various modalities have been reported as the use of calcitonin, osseous plasty surgery, curettage, orthognathic surgery, liposuction and palliative treatments.Institute of Science and Technology of São José dos Campos2015-12-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/vnd.openxmlformats-officedocument.wordprocessingml.documentimage/jpegimage/jpegimage/jpegimage/jpegimage/jpegimage/jpegimage/jpeghttps://ojs.ict.unesp.br/index.php/cob/article/view/113710.14295/bds.2015.v18i4.1137Brazilian Dental Science; Vol. 18 No. 4 (2015): Oct. - Dec. / 2015 - Published November 2015; 133-138Brazilian Dental Science; v. 18 n. 4 (2015): Oct. - Dec. / 2015 - Published November 2015; 133-1382178-6011reponame:Brazilian Dental Scienceinstname:Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP)instacron:UNESPenghttps://ojs.ict.unesp.br/index.php/cob/article/view/1137/988https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2386https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2387https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2388https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2389https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2390https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2391https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2392https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2393Copyright (c) 2015 Brazilian Dental Scienceinfo:eu-repo/semantics/openAccessPatussi, CleversonSassi, Laurindo MoacirBixofix, Regiane BenezSilva, William Phillip Pereira daShussel, Juliana Lucena2020-01-28T12:26:08Zoai:ojs.pkp.sfu.ca:article/1137Revistahttp://bds.ict.unesp.br/PUBhttp://ojs.fosjc.unesp.br/index.php/index/oaisergio@fosjc.unesp.br||sergio@fosjc.unesp.br2178-60112178-6011opendoar:2022-11-08T16:30:01.899658Brazilian Dental Science - Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP)true |
dc.title.none.fl_str_mv |
Non-familial Cherubism – Report of a case |
title |
Non-familial Cherubism – Report of a case |
spellingShingle |
Non-familial Cherubism – Report of a case Patussi, Cleverson |
title_short |
Non-familial Cherubism – Report of a case |
title_full |
Non-familial Cherubism – Report of a case |
title_fullStr |
Non-familial Cherubism – Report of a case |
title_full_unstemmed |
Non-familial Cherubism – Report of a case |
title_sort |
Non-familial Cherubism – Report of a case |
author |
Patussi, Cleverson |
author_facet |
Patussi, Cleverson Sassi, Laurindo Moacir Bixofix, Regiane Benez Silva, William Phillip Pereira da Shussel, Juliana Lucena |
author_role |
author |
author2 |
Sassi, Laurindo Moacir Bixofix, Regiane Benez Silva, William Phillip Pereira da Shussel, Juliana Lucena |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Patussi, Cleverson Sassi, Laurindo Moacir Bixofix, Regiane Benez Silva, William Phillip Pereira da Shussel, Juliana Lucena |
description |
Introduction: The Cherubism is a rare disease that affects the middle and lower third of the face in individuals at the time of childhood. It is a rare hereditary benign bone disease with an autosomal dominant inheritance. The familial distribution may affect different generations and isolated non-familial cases have also been reported in literature. Lesions appear as cystic multilocular radiolucencies, histologically, resembles central giant cell granluloma and hyperparathyroidism brown tumor with numerous randomly distributed multinucleated giant cells and vascular spaces within a fibrous connective tissue stroma. Objectives: The aim of this study is to report the importance of the diagnosis of this pathology and the variety of treatments available in the literature, thus guiding to an individualized treatment. Case Report: Caucasian 8 years-old female, in good general condition, was referred to Service of Oral and Maxillofacial Surgery of Erasto Gaertner Hospital (EGH), Curitiba – PR, Brazil, complaining of bilateral swelling of the maxilla and mandible since 4 years-old. Apparently, the girl is the first one who developed the genetic pathology in at least 4 generation of her family. After biopsy, cherubism diagnosis was confirmed and the treatment of choice was periodic monitoring. Discussion: Cherubism studies with long-term follow-up with clinical and radiographic documentation indicate that the spontaneous resolution of bone lesions is rare. Treatment of cherubism is controversial and various modalities have been reported as the use of calcitonin, osseous plasty surgery, curettage, orthognathic surgery, liposuction and palliative treatments. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-12-07 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://ojs.ict.unesp.br/index.php/cob/article/view/1137 10.14295/bds.2015.v18i4.1137 |
url |
https://ojs.ict.unesp.br/index.php/cob/article/view/1137 |
identifier_str_mv |
10.14295/bds.2015.v18i4.1137 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://ojs.ict.unesp.br/index.php/cob/article/view/1137/988 https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2386 https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2387 https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2388 https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2389 https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2390 https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2391 https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2392 https://ojs.ict.unesp.br/index.php/cob/article/view/1137/2393 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2015 Brazilian Dental Science info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2015 Brazilian Dental Science |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf application/vnd.openxmlformats-officedocument.wordprocessingml.document image/jpeg image/jpeg image/jpeg image/jpeg image/jpeg image/jpeg image/jpeg |
dc.publisher.none.fl_str_mv |
Institute of Science and Technology of São José dos Campos |
publisher.none.fl_str_mv |
Institute of Science and Technology of São José dos Campos |
dc.source.none.fl_str_mv |
Brazilian Dental Science; Vol. 18 No. 4 (2015): Oct. - Dec. / 2015 - Published November 2015; 133-138 Brazilian Dental Science; v. 18 n. 4 (2015): Oct. - Dec. / 2015 - Published November 2015; 133-138 2178-6011 reponame:Brazilian Dental Science instname:Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Brazilian Dental Science |
collection |
Brazilian Dental Science |
repository.name.fl_str_mv |
Brazilian Dental Science - Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP) |
repository.mail.fl_str_mv |
sergio@fosjc.unesp.br||sergio@fosjc.unesp.br |
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1788346899341770752 |