Clinical characterization of anophthalmic and microphthalmic cavities in individuals with craniofacial anomalies

Detalhes bibliográficos
Autor(a) principal: Paula, Isabella de Oliveira Lima Parizotto
Data de Publicação: 2022
Tipo de documento: Dissertação
Idioma: eng
Título da fonte: Biblioteca Digital de Teses e Dissertações da USP
Texto Completo: https://www.teses.usp.br/teses/disponiveis/61/61132/tde-06092022-161354/
Resumo: Objective: Measure the frequency of anophthalmic and microphthalmic patients with craniofacial anomalies (FCAs). Design Descriptive, cross-sectional, retrospective study.Setting Hospital for Rehabilitation in Craniofacial Anomalies of the University of São Paulo (HRAC-USP, Bauru, São Paulo, Brazil). Patients The medical records of patients treated at HRAC from 2000 to 2012 with a diagnosis of anophthalmia or congenital microphthalmia were examined. Patients were excluded for secondary anophthalmia, incomplete medical records, or information that could not be accessed. Outcome Measures Frequency of anophthalmia and microphthalmia; the proportions and diagnoses of associated FCAs; impairment of ocular appendages; extracranial or facial anomalies; genetic alterations; and surgical approach. Results A total of 56 patients had anophthalmia (52.3%), 35 had microphthalmia (32.7%), and 16 patients had both (15%). Individuals with FCAs associated with microphthalmia, anophthalmia, or both totaled 74, corresponding to 69.2%. Anophthalmia was more likely than microphthalmia to be accompanied by FCAs, at 76.4% of patients (p < 0.05). Cleft lip and palate were the main malformations associated with anophthalmia (23.64%), with microphthalmia (45%), and with both (44.44%). Reconstructive surgery was done in 63.6% of cases. The ocular attachments were compromised in 71% of cases. Extracraniofacial malformations were found in 9.3% of patients. Only seven records contained karyotypes, and no changes directly related to anophthalmia or microphthalmia were found. Conclusion Anophthalmia is more frequent than microphthalmia and is more often accompanied by FCA. Cleft lip and cleft palate are the most frequent concomitant malformations.
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spelling Clinical characterization of anophthalmic and microphthalmic cavities in individuals with craniofacial anomaliesCaracterização clínica de cavidades anoftálmicas e microftaálmicas em indivíduos com anomalias craniofaciaisAnoftalmiaAnomalias craniofaciasAnophthalmosCraniofacial abnormalitiesMicroftalmiaMicrophthalmosOrbitÓrbitaObjective: Measure the frequency of anophthalmic and microphthalmic patients with craniofacial anomalies (FCAs). Design Descriptive, cross-sectional, retrospective study.Setting Hospital for Rehabilitation in Craniofacial Anomalies of the University of São Paulo (HRAC-USP, Bauru, São Paulo, Brazil). Patients The medical records of patients treated at HRAC from 2000 to 2012 with a diagnosis of anophthalmia or congenital microphthalmia were examined. Patients were excluded for secondary anophthalmia, incomplete medical records, or information that could not be accessed. Outcome Measures Frequency of anophthalmia and microphthalmia; the proportions and diagnoses of associated FCAs; impairment of ocular appendages; extracranial or facial anomalies; genetic alterations; and surgical approach. Results A total of 56 patients had anophthalmia (52.3%), 35 had microphthalmia (32.7%), and 16 patients had both (15%). Individuals with FCAs associated with microphthalmia, anophthalmia, or both totaled 74, corresponding to 69.2%. Anophthalmia was more likely than microphthalmia to be accompanied by FCAs, at 76.4% of patients (p < 0.05). Cleft lip and palate were the main malformations associated with anophthalmia (23.64%), with microphthalmia (45%), and with both (44.44%). Reconstructive surgery was done in 63.6% of cases. The ocular attachments were compromised in 71% of cases. Extracraniofacial malformations were found in 9.3% of patients. Only seven records contained karyotypes, and no changes directly related to anophthalmia or microphthalmia were found. Conclusion Anophthalmia is more frequent than microphthalmia and is more often accompanied by FCA. Cleft lip and cleft palate are the most frequent concomitant malformations.Objetivo: Frequência de pacientes anoftálmicos e microftálmicos com as anomalias craniofaciais (ACF). Desenho Estudo descritivo, transversal e retrospectivo. Local: Hospital de Reabilitação em Anomalias Craniofaciais da Universidade de São Paulo (HRAC-USP). Bauru, São Paulo, Brasil. Pacientes: Prontuários de pacientes atendidos no HRAC no intervalo do ano de 2000 a 2012 com diagnóstico de anoftalmia ou microftalmia congênita. Excluiu-se anoftalmia secundária, prontuários incompletos ou cujas informações não possam ser acessadas. Desfechos estudados: Frequência de anoftalmia e microftalmia, proporção e diagnóstico de ACF associadas. Comprometimento de anexos oculares, anomalias extracranianas ou faciais, alterações genéticas e abordagem cirúrgica. Resultados: Total de 56 pacientes com anoftalmia (52,3%), 35 com microftalmia (32,7%) e 16 que apresentavam ambos (15%). Indivíduos com ACF associadas a microftalmia, anoftalmia ou ambos somaram 74, correspondendo a 69,2%. Em anoftalmia foi encontrado maior tendência a associar-se com ACF com 76,4% (p<0.05). Fissura labiopalatina foi a principal malformação associada à anoftalmia 23,64%, microftalmia 45% e ambos 44,44% em todas as situações. A cirurgia reparadora ocorreu em 63,6% dos casos. Os anexos oculares foram comprometidos em 71% dos casos. Em 9,3% dos pacientes encontrou-se malformações extra craniofaciais. Apenas 7 prontuários contavam análise de cariótipo e nenhuma alteração diretamente relacionada com a anoftalmia ou microftalmia foi encontrada. Conclusão: Conclui-se que a anoftalmia é mais frequente e que mais se associa a ACF. As fissuras labiopalatinas são as malformações concomitantes mais frequentes.Biblioteca Digitais de Teses e Dissertações da USPTonello, CristianoPaula, Isabella de Oliveira Lima Parizotto2022-07-22info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttps://www.teses.usp.br/teses/disponiveis/61/61132/tde-06092022-161354/reponame:Biblioteca Digital de Teses e Dissertações da USPinstname:Universidade de São Paulo (USP)instacron:USPLiberar o conteúdo para acesso público.info:eu-repo/semantics/openAccesseng2024-10-09T13:16:04Zoai:teses.usp.br:tde-06092022-161354Biblioteca Digital de Teses e Dissertaçõeshttp://www.teses.usp.br/PUBhttp://www.teses.usp.br/cgi-bin/mtd2br.plvirginia@if.usp.br|| atendimento@aguia.usp.br||virginia@if.usp.bropendoar:27212024-10-09T13:16:04Biblioteca Digital de Teses e Dissertações da USP - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Clinical characterization of anophthalmic and microphthalmic cavities in individuals with craniofacial anomalies
Caracterização clínica de cavidades anoftálmicas e microftaálmicas em indivíduos com anomalias craniofaciais
title Clinical characterization of anophthalmic and microphthalmic cavities in individuals with craniofacial anomalies
spellingShingle Clinical characterization of anophthalmic and microphthalmic cavities in individuals with craniofacial anomalies
Paula, Isabella de Oliveira Lima Parizotto
Anoftalmia
Anomalias craniofacias
Anophthalmos
Craniofacial abnormalities
Microftalmia
Microphthalmos
Orbit
Órbita
title_short Clinical characterization of anophthalmic and microphthalmic cavities in individuals with craniofacial anomalies
title_full Clinical characterization of anophthalmic and microphthalmic cavities in individuals with craniofacial anomalies
title_fullStr Clinical characterization of anophthalmic and microphthalmic cavities in individuals with craniofacial anomalies
title_full_unstemmed Clinical characterization of anophthalmic and microphthalmic cavities in individuals with craniofacial anomalies
title_sort Clinical characterization of anophthalmic and microphthalmic cavities in individuals with craniofacial anomalies
author Paula, Isabella de Oliveira Lima Parizotto
author_facet Paula, Isabella de Oliveira Lima Parizotto
author_role author
dc.contributor.none.fl_str_mv Tonello, Cristiano
dc.contributor.author.fl_str_mv Paula, Isabella de Oliveira Lima Parizotto
dc.subject.por.fl_str_mv Anoftalmia
Anomalias craniofacias
Anophthalmos
Craniofacial abnormalities
Microftalmia
Microphthalmos
Orbit
Órbita
topic Anoftalmia
Anomalias craniofacias
Anophthalmos
Craniofacial abnormalities
Microftalmia
Microphthalmos
Orbit
Órbita
description Objective: Measure the frequency of anophthalmic and microphthalmic patients with craniofacial anomalies (FCAs). Design Descriptive, cross-sectional, retrospective study.Setting Hospital for Rehabilitation in Craniofacial Anomalies of the University of São Paulo (HRAC-USP, Bauru, São Paulo, Brazil). Patients The medical records of patients treated at HRAC from 2000 to 2012 with a diagnosis of anophthalmia or congenital microphthalmia were examined. Patients were excluded for secondary anophthalmia, incomplete medical records, or information that could not be accessed. Outcome Measures Frequency of anophthalmia and microphthalmia; the proportions and diagnoses of associated FCAs; impairment of ocular appendages; extracranial or facial anomalies; genetic alterations; and surgical approach. Results A total of 56 patients had anophthalmia (52.3%), 35 had microphthalmia (32.7%), and 16 patients had both (15%). Individuals with FCAs associated with microphthalmia, anophthalmia, or both totaled 74, corresponding to 69.2%. Anophthalmia was more likely than microphthalmia to be accompanied by FCAs, at 76.4% of patients (p < 0.05). Cleft lip and palate were the main malformations associated with anophthalmia (23.64%), with microphthalmia (45%), and with both (44.44%). Reconstructive surgery was done in 63.6% of cases. The ocular attachments were compromised in 71% of cases. Extracraniofacial malformations were found in 9.3% of patients. Only seven records contained karyotypes, and no changes directly related to anophthalmia or microphthalmia were found. Conclusion Anophthalmia is more frequent than microphthalmia and is more often accompanied by FCA. Cleft lip and cleft palate are the most frequent concomitant malformations.
publishDate 2022
dc.date.none.fl_str_mv 2022-07-22
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
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dc.identifier.uri.fl_str_mv https://www.teses.usp.br/teses/disponiveis/61/61132/tde-06092022-161354/
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dc.language.iso.fl_str_mv eng
language eng
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dc.rights.driver.fl_str_mv Liberar o conteúdo para acesso público.
info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Biblioteca Digitais de Teses e Dissertações da USP
publisher.none.fl_str_mv Biblioteca Digitais de Teses e Dissertações da USP
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reponame:Biblioteca Digital de Teses e Dissertações da USP
instname:Universidade de São Paulo (USP)
instacron:USP
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reponame_str Biblioteca Digital de Teses e Dissertações da USP
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