Laboratory and Imaging follow-up of the patient with Boné Paget´s
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , |
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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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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1797052620499582976 |