An Atypical and Severe Case of Neuralgic Amyotrophy

Detalhes bibliográficos
Autor(a) principal: Cadilha, Rui; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
Data de Publicação: 2017
Outros Autores: Amorim, Hugo; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto, Pinto, Madalena; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto, Silveira, Fernando; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto, Parada, Fernando; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.25759/spmfr.267
Resumo: Neuralgic amyotrophy or Parsonage-Turner syndrome is an uncommon disorder, of unknown etiology, typically characterized by abrupt onset of shoulder and upper extremity pain followed by progressive neurologic deficits. An immune/autoimmune process seems to have more support in development of neuralgic amyotrophy. Neuralgic amyotrophy is a clinical diagnosis, however, further diagnostic studies can confirm clinical suspicion and help exclude other causes. The treatment consists predominantly in pain control and rehabilitation. Patients with neuralgic amyotrophy, can be evaluated by a wide range of clinical specialists in the early stage of disease before a correct diagnosis be made. This is a result of different phenotypes that this disorder exhibits, that complicate the diagnosis. It is important for clinicians to beware of the classic clinical manifestations that usually follow a characteristic clinical course of abrupt onset of shoulder girdle pain followed by progressive neurologic deficits as muscle weakness, amyotrophy and sensory abnormalities. We report the case of a 32-year-old man who had a severe bilateral and atypical shoulder involvement, that made the most probably diagnostic not so evident.
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spelling An Atypical and Severe Case of Neuralgic AmyotrophyUm Caso Atípico e Grave de Amiotrofia NeurálgicaBrachial Plexus Neuritis; Shoulder PainDor de Ombro; Neurite do Plexo BraquialNeuralgic amyotrophy or Parsonage-Turner syndrome is an uncommon disorder, of unknown etiology, typically characterized by abrupt onset of shoulder and upper extremity pain followed by progressive neurologic deficits. An immune/autoimmune process seems to have more support in development of neuralgic amyotrophy. Neuralgic amyotrophy is a clinical diagnosis, however, further diagnostic studies can confirm clinical suspicion and help exclude other causes. The treatment consists predominantly in pain control and rehabilitation. Patients with neuralgic amyotrophy, can be evaluated by a wide range of clinical specialists in the early stage of disease before a correct diagnosis be made. This is a result of different phenotypes that this disorder exhibits, that complicate the diagnosis. It is important for clinicians to beware of the classic clinical manifestations that usually follow a characteristic clinical course of abrupt onset of shoulder girdle pain followed by progressive neurologic deficits as muscle weakness, amyotrophy and sensory abnormalities. We report the case of a 32-year-old man who had a severe bilateral and atypical shoulder involvement, that made the most probably diagnostic not so evident.A amiotrofia neurálgica ou síndroma de Parsonage-Turner é uma síndrome incomum, de etiologia desconhecida, tipicamente caracterizada pelo início súbito de dor nos ombros e/ou membros superiores seguida de défices neurológicos progressivos. Um processo imune/autoimune parece estar na origem desta síndrome. A amiotrofia neurálgica é um diagnóstico clínico, no entanto, os exames complementares podem ajudar a confirmar a suspeita clínica e a excluir outras patologias. O tratamento consiste predominantemente no controlo da dor e reabilitação. Os pacientes com amiotrofia neurálgica podem ser avaliados por um vasto número de clínicos na fase inicial da doença antes de ser efetuado o diagnóstico correto. Este atraso é resultado dos diferentes fenótipos que esta síndrome pode exibir, complicando o diagnóstico. É importante que os clínicos tenham presentes as manifestações clínicas clássicas que geralmente seguem um curso característico com início abrupto de dor na cintura escapular seguido de deficits neurológicos progressivos como fraqueza muscular, amiotrofia e alterações sensitivas. Apresentamos o caso clínico de um homem de 32 anos com atingimento bilateral grave e atípico, o que fez com que o diagnóstico mais provável não fosse tão evidente.Sociedade Portuguesa de Medicina Física e de Reabilitação2017-12-23T00:00:00Zjournal articlejournal articleinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://doi.org/10.25759/spmfr.267oai:ojs.spmfrjournal.org:article/267Revista da Sociedade Portuguesa de Medicina Física e de Reabilitação; v. 29, n. 2 (2017): Ano 25; 36-400872-9204reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://spmfrjournal.org/index.php/spmfr/article/view/267https://doi.org/10.25759/spmfr.267https://spmfrjournal.org/index.php/spmfr/article/view/267/145Copyright (c) 2017 Revista da Sociedade Portuguesa de Medicina Física e de Reabilitaçãoinfo:eu-repo/semantics/openAccessCadilha, Rui; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, PortoAmorim, Hugo; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, PortoPinto, Madalena; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, PortoSilveira, Fernando; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, PortoParada, Fernando; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto2022-09-20T15:28:44Zoai:ojs.spmfrjournal.org:article/267Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:51:18.638691Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv An Atypical and Severe Case of Neuralgic Amyotrophy
Um Caso Atípico e Grave de Amiotrofia Neurálgica
title An Atypical and Severe Case of Neuralgic Amyotrophy
spellingShingle An Atypical and Severe Case of Neuralgic Amyotrophy
Cadilha, Rui; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
Brachial Plexus Neuritis; Shoulder Pain
Dor de Ombro; Neurite do Plexo Braquial
title_short An Atypical and Severe Case of Neuralgic Amyotrophy
title_full An Atypical and Severe Case of Neuralgic Amyotrophy
title_fullStr An Atypical and Severe Case of Neuralgic Amyotrophy
title_full_unstemmed An Atypical and Severe Case of Neuralgic Amyotrophy
title_sort An Atypical and Severe Case of Neuralgic Amyotrophy
author Cadilha, Rui; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
author_facet Cadilha, Rui; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
Amorim, Hugo; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
Pinto, Madalena; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
Silveira, Fernando; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
Parada, Fernando; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
author_role author
author2 Amorim, Hugo; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
Pinto, Madalena; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
Silveira, Fernando; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
Parada, Fernando; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Cadilha, Rui; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
Amorim, Hugo; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
Pinto, Madalena; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
Silveira, Fernando; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
Parada, Fernando; Department of Physical and Rehabilitation Medicine, Centro Hospitalar São João, Porto
dc.subject.por.fl_str_mv Brachial Plexus Neuritis; Shoulder Pain
Dor de Ombro; Neurite do Plexo Braquial
topic Brachial Plexus Neuritis; Shoulder Pain
Dor de Ombro; Neurite do Plexo Braquial
description Neuralgic amyotrophy or Parsonage-Turner syndrome is an uncommon disorder, of unknown etiology, typically characterized by abrupt onset of shoulder and upper extremity pain followed by progressive neurologic deficits. An immune/autoimmune process seems to have more support in development of neuralgic amyotrophy. Neuralgic amyotrophy is a clinical diagnosis, however, further diagnostic studies can confirm clinical suspicion and help exclude other causes. The treatment consists predominantly in pain control and rehabilitation. Patients with neuralgic amyotrophy, can be evaluated by a wide range of clinical specialists in the early stage of disease before a correct diagnosis be made. This is a result of different phenotypes that this disorder exhibits, that complicate the diagnosis. It is important for clinicians to beware of the classic clinical manifestations that usually follow a characteristic clinical course of abrupt onset of shoulder girdle pain followed by progressive neurologic deficits as muscle weakness, amyotrophy and sensory abnormalities. We report the case of a 32-year-old man who had a severe bilateral and atypical shoulder involvement, that made the most probably diagnostic not so evident.
publishDate 2017
dc.date.none.fl_str_mv 2017-12-23T00:00:00Z
dc.type.driver.fl_str_mv journal article
journal article
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dc.identifier.uri.fl_str_mv https://doi.org/10.25759/spmfr.267
oai:ojs.spmfrjournal.org:article/267
url https://doi.org/10.25759/spmfr.267
identifier_str_mv oai:ojs.spmfrjournal.org:article/267
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dc.relation.none.fl_str_mv https://spmfrjournal.org/index.php/spmfr/article/view/267
https://doi.org/10.25759/spmfr.267
https://spmfrjournal.org/index.php/spmfr/article/view/267/145
dc.rights.driver.fl_str_mv Copyright (c) 2017 Revista da Sociedade Portuguesa de Medicina Física e de Reabilitação
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2017 Revista da Sociedade Portuguesa de Medicina Física e de Reabilitação
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Sociedade Portuguesa de Medicina Física e de Reabilitação
publisher.none.fl_str_mv Sociedade Portuguesa de Medicina Física e de Reabilitação
dc.source.none.fl_str_mv Revista da Sociedade Portuguesa de Medicina Física e de Reabilitação; v. 29, n. 2 (2017): Ano 25; 36-40
0872-9204
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