Laboratory and Imaging follow-up of the patient with Boné Paget´s

Detalhes bibliográficos
Autor(a) principal: Andrade, Glória Maria Barroso Rodrigues
Data de Publicação: 2023
Outros Autores: Lima Júnior , Francisco Jucier de, Tavares Neto, Manoel Edenor, Brito, Carla Maria Soares, Souza, Luan Kelves Miranda de
Tipo de documento: Artigo
Idioma: por
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/40735
Resumo: Paget's Disease of Bone (POD) has a viral and/or hereditary etiology, its strong familial component is noticeable, since 40% of patients have a family history of the disease, strengthening the idea that there is an autosomal dominant inheritance pattern. The main follow-up method used for patients with POP is the measurement of serum alkaline phosphatase, which is also used to assess the initial response to treatment. The purpose of this bibliographical study is to present, synthesize and describe the most relevant aspects that guide the medical follow-up of patients diagnosed with Paget's Disease of Bone, in order to cite and analyze the importance of medical action in the care of these patients, in an attempt to generate knowledge and updates that help in dealing with these patients, above all, to avoid the evolution of the disease and the appearance of possible complications. UpToDate, Scielo, Virtual Health Library (VHL), PubMed and ebscohost were used as databases, using the following descriptors: Paget's disease, laboratory monitoring, imaging tests, genetics and complications. The pagetic patient can evolve with osteosarcoma, irreversible hearing loss and paraplegia, making its multidisciplinary follow-up essential, through serum and bone alkaline phosphatase dosages, as well as the use of imaging tests, such as scintigraphy and radiography, for research of structural complications or neoplastic transformations, aiming at symptomatic relief along with delaying the progression of the disease, avoiding the total disability of the patient.
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spelling Laboratory and Imaging follow-up of the patient with Boné Paget´s Seguimiento de laboratório e imagen del paciente con Enfermiedad de Paget Óseo Acompanhamento laboratorial e por imagem do paciente com Doença de Paget ÓsseaPaget's diseaseMedical examinationLaboratory diagnosis.Enfermedad de PagetExamen medicalDiagnóstico de laboratório. Doença de PagetExames médicosDiagnóstico laboratorial.Paget's Disease of Bone (POD) has a viral and/or hereditary etiology, its strong familial component is noticeable, since 40% of patients have a family history of the disease, strengthening the idea that there is an autosomal dominant inheritance pattern. The main follow-up method used for patients with POP is the measurement of serum alkaline phosphatase, which is also used to assess the initial response to treatment. The purpose of this bibliographical study is to present, synthesize and describe the most relevant aspects that guide the medical follow-up of patients diagnosed with Paget's Disease of Bone, in order to cite and analyze the importance of medical action in the care of these patients, in an attempt to generate knowledge and updates that help in dealing with these patients, above all, to avoid the evolution of the disease and the appearance of possible complications. UpToDate, Scielo, Virtual Health Library (VHL), PubMed and ebscohost were used as databases, using the following descriptors: Paget's disease, laboratory monitoring, imaging tests, genetics and complications. The pagetic patient can evolve with osteosarcoma, irreversible hearing loss and paraplegia, making its multidisciplinary follow-up essential, through serum and bone alkaline phosphatase dosages, as well as the use of imaging tests, such as scintigraphy and radiography, for research of structural complications or neoplastic transformations, aiming at symptomatic relief along with delaying the progression of the disease, avoiding the total disability of the patient.La Enfermedad Ósea de Paget (EPO) tiene una etiología viral y/o hereditaria, es notorio su fuerte componente familiar, ya que el 40% de los pacientes tienen antecedentes familiares de la enfermedad, reforzando la idea de que existe un patrón de herencia autosómico dominante. El principal método de seguimiento utilizado para los pacientes con POP es la medición de la fosfatasa alcalina sérica, que también se utiliza para evaluar la respuesta inicial al tratamiento. El presente estudio bibliográfico tiene como objetivo presentar, sintetizar y describir los aspectos más relevantes que orientan el seguimiento médico de los pacientes con diagnóstico de Enfermedad Ósea de Paget, con el fin de citar y analizar la importancia de la actuación médica en la atención de estos pacientes. , en un intento de generar conocimientos y actualizaciones que ayuden en el abordaje de estos pacientes, sobre todo, para evitar la evolución de la enfermedad y la aparición de posibles complicaciones. Se utilizaron como bases de datos UpToDate, Scielo, Biblioteca Virtual en Salud (BVS), PubMed y ebscohost, utilizando los siguientes descriptores: enfermedad de Paget, seguimiento de laboratorio, pruebas de imagen, genética y complicaciones. El paciente pagético puede evolucionar con osteosarcoma, hipoacusia irreversible y paraplejia, siendo imprescindible su seguimiento multidisciplinar, mediante dosificación de fosfatasa alcalina sérica y ósea, así como la utilización de pruebas de imagen, como gammagrafía y radiografía, para la investigación de complicaciones estructurales. o transformaciones neoplásicas, buscando el alivio sintomático junto con retrasar la progresión de la enfermedad, evitando la invalidez total del paciente.A Doença de Paget Óssea (DPO) possui etiologia viral e/ou hereditário, seu forte componente familiar é perceptível, visto que, 40% dos pacientes possuem histórico familiar da doença, fortalecendo a ideia de que haja um padrão de herança autossômica dominante. O principal método de acompanhamento utilizado para pacientes com DPO, é a dosagem de fosfatase alcalina sérica, empregada também na avaliação da resposta inicial ao tratamento. O presente estudo bibliográfico tem por finalidade apresentar, sintetizar e descrever os aspectos mais relevantes que norteia o acompanhamento médico de pacientes diagnosticados com Doença de Paget Óssea, a fim de citar e analisar a importância da atuação médica nos cuidados desses pacientes, na tentativa gerar conhecimento e atualizações que auxiliem na lida desses pacientes, sobretudo, para evitar a evolução da doença e o surgimento de possíveis complicações.  Utilizou-se como base de dados o UpToDate, Scielo, Biblioteca Virtual em Saúde (BVS), PubMed e ebscohost a partir dos seguintes descritores: Doença de Paget, acompanhamento laboratorial, exames de imagem, genética e complicações. O paciente pagético pode evoluir com osteosarcoma, perda auditiva irreversível e paraplegia, tornando indispensável o seu acompanhamento multidisciplinar, através de dosagens de fosfatase alcalina sérica e óssea, assim como o uso de exames de imagem, como a cintilografia e a radiografia, para a pesquisa de complicações estruturais ou transformações neoplásicas, objetivando o alívio sintomatológico juntamente ao retardo da progressão da doença, evitando a invalidez total do paciente. Research, Society and Development2023-03-14info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/4073510.33448/rsd-v12i3.40735Research, Society and Development; Vol. 12 No. 3; e21912340735Research, Society and Development; Vol. 12 Núm. 3; e21912340735Research, Society and Development; v. 12 n. 3; e219123407352525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/40735/33213Copyright (c) 2023 Glória Maria Barroso Rodrigues Andrade; Francisco Jucier de Lima Júnior ; Manoel Edenor Tavares Neto; Carla Maria Soares Brito; Luan Kelves Miranda de Souzahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessAndrade, Glória Maria Barroso Rodrigues Lima Júnior , Francisco Jucier de Tavares Neto, Manoel Edenor Brito, Carla Maria Soares Souza, Luan Kelves Miranda de 2023-03-23T08:33:38Zoai:ojs.pkp.sfu.ca:article/40735Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2023-03-23T08:33:38Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Laboratory and Imaging follow-up of the patient with Boné Paget´s
Seguimiento de laboratório e imagen del paciente con Enfermiedad de Paget Óseo
Acompanhamento laboratorial e por imagem do paciente com Doença de Paget Óssea
title Laboratory and Imaging follow-up of the patient with Boné Paget´s
spellingShingle Laboratory and Imaging follow-up of the patient with Boné Paget´s
Andrade, Glória Maria Barroso Rodrigues
Paget's disease
Medical examination
Laboratory diagnosis.
Enfermedad de Paget
Examen medical
Diagnóstico de laboratório.
Doença de Paget
Exames médicos
Diagnóstico laboratorial.
title_short Laboratory and Imaging follow-up of the patient with Boné Paget´s
title_full Laboratory and Imaging follow-up of the patient with Boné Paget´s
title_fullStr Laboratory and Imaging follow-up of the patient with Boné Paget´s
title_full_unstemmed Laboratory and Imaging follow-up of the patient with Boné Paget´s
title_sort Laboratory and Imaging follow-up of the patient with Boné Paget´s
author Andrade, Glória Maria Barroso Rodrigues
author_facet Andrade, Glória Maria Barroso Rodrigues
Lima Júnior , Francisco Jucier de
Tavares Neto, Manoel Edenor
Brito, Carla Maria Soares
Souza, Luan Kelves Miranda de
author_role author
author2 Lima Júnior , Francisco Jucier de
Tavares Neto, Manoel Edenor
Brito, Carla Maria Soares
Souza, Luan Kelves Miranda de
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Andrade, Glória Maria Barroso Rodrigues
Lima Júnior , Francisco Jucier de
Tavares Neto, Manoel Edenor
Brito, Carla Maria Soares
Souza, Luan Kelves Miranda de
dc.subject.por.fl_str_mv Paget's disease
Medical examination
Laboratory diagnosis.
Enfermedad de Paget
Examen medical
Diagnóstico de laboratório.
Doença de Paget
Exames médicos
Diagnóstico laboratorial.
topic Paget's disease
Medical examination
Laboratory diagnosis.
Enfermedad de Paget
Examen medical
Diagnóstico de laboratório.
Doença de Paget
Exames médicos
Diagnóstico laboratorial.
description Paget's Disease of Bone (POD) has a viral and/or hereditary etiology, its strong familial component is noticeable, since 40% of patients have a family history of the disease, strengthening the idea that there is an autosomal dominant inheritance pattern. The main follow-up method used for patients with POP is the measurement of serum alkaline phosphatase, which is also used to assess the initial response to treatment. The purpose of this bibliographical study is to present, synthesize and describe the most relevant aspects that guide the medical follow-up of patients diagnosed with Paget's Disease of Bone, in order to cite and analyze the importance of medical action in the care of these patients, in an attempt to generate knowledge and updates that help in dealing with these patients, above all, to avoid the evolution of the disease and the appearance of possible complications. UpToDate, Scielo, Virtual Health Library (VHL), PubMed and ebscohost were used as databases, using the following descriptors: Paget's disease, laboratory monitoring, imaging tests, genetics and complications. The pagetic patient can evolve with osteosarcoma, irreversible hearing loss and paraplegia, making its multidisciplinary follow-up essential, through serum and bone alkaline phosphatase dosages, as well as the use of imaging tests, such as scintigraphy and radiography, for research of structural complications or neoplastic transformations, aiming at symptomatic relief along with delaying the progression of the disease, avoiding the total disability of the patient.
publishDate 2023
dc.date.none.fl_str_mv 2023-03-14
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://rsdjournal.org/index.php/rsd/article/view/40735
10.33448/rsd-v12i3.40735
url https://rsdjournal.org/index.php/rsd/article/view/40735
identifier_str_mv 10.33448/rsd-v12i3.40735
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/40735/33213
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Research, Society and Development
publisher.none.fl_str_mv Research, Society and Development
dc.source.none.fl_str_mv Research, Society and Development; Vol. 12 No. 3; e21912340735
Research, Society and Development; Vol. 12 Núm. 3; e21912340735
Research, Society and Development; v. 12 n. 3; e21912340735
2525-3409
reponame:Research, Society and Development
instname:Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
instname_str Universidade Federal de Itajubá (UNIFEI)
instacron_str UNIFEI
institution UNIFEI
reponame_str Research, Society and Development
collection Research, Society and Development
repository.name.fl_str_mv Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)
repository.mail.fl_str_mv rsd.articles@gmail.com
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