Dentinogênese imperfeita tipo II: um relato de caso com acompanhamento de 34 anos

Detalhes bibliográficos
Autor(a) principal: Vieira, Heloisa Aparecida Orsini
Data de Publicação: 2020
Outros Autores: Freitas, Aldevina Campos de, Fernandes, Regina Maura, Longo, Daniele Lucca, Silva, Raquel Assed Bezerra da, Daltoé, Mariana de Oliveira, Queiroz, Alexandra Mussolino de, Nelson Filho, Paulo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinical and Laboratorial Research in Dentistry
Texto Completo: https://www.revistas.usp.br/clrd/article/view/168679
Resumo: Dentinogenesis imperfecta (DI) is a hereditary developmental disorder of dentin formation that can occur associated with osteogenesis imperfecta (type I), isolated (type II), or in a specific isolated resident group of Brandywine, in southern Maryland (type III). This work aims at reporting a clinical case of DI type II in childhood with a 34-year follow up. The child at issue was taken to the dental health service at a very young age, which favored an appropriate treatment, avoiding complications, and portending a favorable long-term prognosis, besides safeguarding the patient physical and mental well-being. The clinical aspects of this condition are teeth with short crowns and gray-brown coloration, and an altered consistency of affected dental elements. Radiographically, the teeth present bulbous crowns, cervical constriction, thin roots, and early obliteration of the root canal and pulp chambers due to excessive dentin production. Rehabilitation treatment included the use of stainless-steel crowns for reconstructing deciduous molars and composite resin restorations on the anterior deciduous teeth. As for permanent dentition, it consisted of aesthetic-functional rehabilitation using metal crowns on the first molars and ceramic crowns and facets on the anterior teeth. Endodontic, prosthetic and restorative treatment was performed on other posterior teeth. Preventive measures were instituted. DI may cause serious changes in dentin structure, affecting function and aesthetics in both dentitions. The sooner it is administered, the more promising the multidisciplinary dental treatment will be in promoting health and minimizing damage to affected individuals.
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spelling Dentinogênese imperfeita tipo II: um relato de caso com acompanhamento de 34 anosDentinogenesis imperfecta type II: a case report of a 34-year follow-upDentinogênese ImperfeitaDiagnóstico PrecoceReabilitação oralContinuidade da Assistência ao PacienteDentinogenesis ImperfectaEarly DiagnosisMouth RehabilitationContinuity of Patient CareDentinogenesis imperfecta (DI) is a hereditary developmental disorder of dentin formation that can occur associated with osteogenesis imperfecta (type I), isolated (type II), or in a specific isolated resident group of Brandywine, in southern Maryland (type III). This work aims at reporting a clinical case of DI type II in childhood with a 34-year follow up. The child at issue was taken to the dental health service at a very young age, which favored an appropriate treatment, avoiding complications, and portending a favorable long-term prognosis, besides safeguarding the patient physical and mental well-being. The clinical aspects of this condition are teeth with short crowns and gray-brown coloration, and an altered consistency of affected dental elements. Radiographically, the teeth present bulbous crowns, cervical constriction, thin roots, and early obliteration of the root canal and pulp chambers due to excessive dentin production. Rehabilitation treatment included the use of stainless-steel crowns for reconstructing deciduous molars and composite resin restorations on the anterior deciduous teeth. As for permanent dentition, it consisted of aesthetic-functional rehabilitation using metal crowns on the first molars and ceramic crowns and facets on the anterior teeth. Endodontic, prosthetic and restorative treatment was performed on other posterior teeth. Preventive measures were instituted. DI may cause serious changes in dentin structure, affecting function and aesthetics in both dentitions. The sooner it is administered, the more promising the multidisciplinary dental treatment will be in promoting health and minimizing damage to affected individuals.A dentinogênese imperfeita (DI) é uma doença de alteração hereditária que afeta o desenvolvimento dentinário, podendo ocorrer associada à presença de osteogênese imperfeita (tipo I), isoladamente (tipo II), ou especificamente associada ao povoado de Brandywine, no sul de Maryland (tipo III). O objetivo deste trabalho é relatar um caso clínico de DI tipo II na infância que recebeu acompanhamento por 34 anos. A criança em questão foi encaminhada ao serviço de assistência odontológica ainda muito pequena, o que favoreceu um tratamento adequado, evitando complicações e trazendo um prognóstico favorável a longo prazo, além de garantir o bem-estar físico e mental da paciente. Os aspectos clínicos desta condição são dentes com coroas curtas e coloração marrom acinzentada, além de uma consistência alterada nos elementos dentários afetados. Radiograficamente, foram identificados dentes com coroas bulbosas, constrição cervical, raízes afinadas, e obliteração precoce do canal radicular e câmaras pulpares devido à excessiva produção de dentina. Para o tratamento, utilizou-se coroas de aço cromado na reconstrução de molares decíduos e restaurações de resina composta nos dentes decíduos anteriores. Quanto à dentição permanente, o tratamento visou reestabelecer a função e a estética, utilizando-se de coroas metálicas nos primeiros molares e coroas e facetas cerâmicas nos dentes anteriores. Em outros dentes posteriores foram utilizados os tratamentos endodôntico, protético e restaurador. Medidas preventivas foram instituídas. Em conclusão, a DI pode causar sérias alterações na estrutura dentinária, afetando a função e a estética de ambas as dentições. A intervenção odontológica multidisciplinar será mais promissora quanto mais cedo for estabelecida, promovendo a saúde bucal e minimizando os danos aos indivíduos afetados.Universidade de São Paulo. Faculdade de Odontologia2020-09-24info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clrd/article/view/16867910.11606/issn.2357-8041.clrd.2020.168679Clinical and Laboratorial Research in Dentistry; 2020Clinical and Laboratorial Research in Dentistry; 20202357-8041reponame:Clinical and Laboratorial Research in Dentistryinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clrd/article/view/168679/163526Copyright (c) 2020 Heloisa Aparecida Orsini Vieira, DDS, Aldevina Campos de Freitas, PhD, Regina Maura Fernandes, PhD, Daniele Lucca Longo, PhD, Raquel Assed Bezerra da Silva, PhD, Mariana de Oliveira Daltoé, MSc, Alexandra Mussolino de Queiroz, PhD, Paulo Nelson Filho, PhDhttp://creativecommons.org/licenses/by-nc/4.0info:eu-repo/semantics/openAccessVieira, Heloisa Aparecida OrsiniFreitas, Aldevina Campos deFernandes, Regina MauraLongo, Daniele LuccaSilva, Raquel Assed Bezerra daDaltoé, Mariana de OliveiraQueiroz, Alexandra Mussolino deNelson Filho, Paulo2020-09-30T19:19:47ZRevistahttp://www.revistas.usp.br/clrd/indexPUB
dc.title.none.fl_str_mv Dentinogênese imperfeita tipo II: um relato de caso com acompanhamento de 34 anos
Dentinogenesis imperfecta type II: a case report of a 34-year follow-up
title Dentinogênese imperfeita tipo II: um relato de caso com acompanhamento de 34 anos
spellingShingle Dentinogênese imperfeita tipo II: um relato de caso com acompanhamento de 34 anos
Vieira, Heloisa Aparecida Orsini
Dentinogênese Imperfeita
Diagnóstico Precoce
Reabilitação oral
Continuidade da Assistência ao Paciente
Dentinogenesis Imperfecta
Early Diagnosis
Mouth Rehabilitation
Continuity of Patient Care
title_short Dentinogênese imperfeita tipo II: um relato de caso com acompanhamento de 34 anos
title_full Dentinogênese imperfeita tipo II: um relato de caso com acompanhamento de 34 anos
title_fullStr Dentinogênese imperfeita tipo II: um relato de caso com acompanhamento de 34 anos
title_full_unstemmed Dentinogênese imperfeita tipo II: um relato de caso com acompanhamento de 34 anos
title_sort Dentinogênese imperfeita tipo II: um relato de caso com acompanhamento de 34 anos
author Vieira, Heloisa Aparecida Orsini
author_facet Vieira, Heloisa Aparecida Orsini
Freitas, Aldevina Campos de
Fernandes, Regina Maura
Longo, Daniele Lucca
Silva, Raquel Assed Bezerra da
Daltoé, Mariana de Oliveira
Queiroz, Alexandra Mussolino de
Nelson Filho, Paulo
author_role author
author2 Freitas, Aldevina Campos de
Fernandes, Regina Maura
Longo, Daniele Lucca
Silva, Raquel Assed Bezerra da
Daltoé, Mariana de Oliveira
Queiroz, Alexandra Mussolino de
Nelson Filho, Paulo
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Vieira, Heloisa Aparecida Orsini
Freitas, Aldevina Campos de
Fernandes, Regina Maura
Longo, Daniele Lucca
Silva, Raquel Assed Bezerra da
Daltoé, Mariana de Oliveira
Queiroz, Alexandra Mussolino de
Nelson Filho, Paulo
dc.subject.por.fl_str_mv Dentinogênese Imperfeita
Diagnóstico Precoce
Reabilitação oral
Continuidade da Assistência ao Paciente
Dentinogenesis Imperfecta
Early Diagnosis
Mouth Rehabilitation
Continuity of Patient Care
topic Dentinogênese Imperfeita
Diagnóstico Precoce
Reabilitação oral
Continuidade da Assistência ao Paciente
Dentinogenesis Imperfecta
Early Diagnosis
Mouth Rehabilitation
Continuity of Patient Care
description Dentinogenesis imperfecta (DI) is a hereditary developmental disorder of dentin formation that can occur associated with osteogenesis imperfecta (type I), isolated (type II), or in a specific isolated resident group of Brandywine, in southern Maryland (type III). This work aims at reporting a clinical case of DI type II in childhood with a 34-year follow up. The child at issue was taken to the dental health service at a very young age, which favored an appropriate treatment, avoiding complications, and portending a favorable long-term prognosis, besides safeguarding the patient physical and mental well-being. The clinical aspects of this condition are teeth with short crowns and gray-brown coloration, and an altered consistency of affected dental elements. Radiographically, the teeth present bulbous crowns, cervical constriction, thin roots, and early obliteration of the root canal and pulp chambers due to excessive dentin production. Rehabilitation treatment included the use of stainless-steel crowns for reconstructing deciduous molars and composite resin restorations on the anterior deciduous teeth. As for permanent dentition, it consisted of aesthetic-functional rehabilitation using metal crowns on the first molars and ceramic crowns and facets on the anterior teeth. Endodontic, prosthetic and restorative treatment was performed on other posterior teeth. Preventive measures were instituted. DI may cause serious changes in dentin structure, affecting function and aesthetics in both dentitions. The sooner it is administered, the more promising the multidisciplinary dental treatment will be in promoting health and minimizing damage to affected individuals.
publishDate 2020
dc.date.none.fl_str_mv 2020-09-24
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dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clrd/article/view/168679
10.11606/issn.2357-8041.clrd.2020.168679
url https://www.revistas.usp.br/clrd/article/view/168679
identifier_str_mv 10.11606/issn.2357-8041.clrd.2020.168679
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clrd/article/view/168679/163526
dc.rights.driver.fl_str_mv http://creativecommons.org/licenses/by-nc/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Odontologia
publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Odontologia
dc.source.none.fl_str_mv Clinical and Laboratorial Research in Dentistry; 2020
Clinical and Laboratorial Research in Dentistry; 2020
2357-8041
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instname_str Universidade de São Paulo (USP)
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