Non-familial Cherubism – Report of a case

Detalhes bibliográficos
Autor(a) principal: Patussi, Cleverson
Data de Publicação: 2015
Outros Autores: Sassi, Laurindo Moacir, Bixofix, Regiane Benez, Silva, William Phillip Pereira da, Shussel, Juliana Lucena
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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spelling 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.
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dc.rights.driver.fl_str_mv Copyright (c) 2015 Brazilian Dental Science
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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
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