Neuroleptic malignant syndrome: a rare long lasting case report.

Detalhes bibliográficos
Autor(a) principal: Lemos, Joana
Data de Publicação: 2010
Outros Autores: Mós, Marta, Monteiro, António, Henriques, Pedro
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/732
Resumo: Neuroleptic malignant syndrome (NMS) is a neurological emergency related to neuroleptics medication. Diagnosis is clinical. Authors present the case of a 32-year-old Caucasian man with a history of moderated oligophreny treated with stable doses of psychotropic and neuroleptic drugs. Because of aggressivity outbreaks, he was administered high doses of intramuscular haloperidol decanoate for a period of ten days. One month later he had evolved with mental deterioration, mutism, generalized rigidity, fever, tachycardia, hypotension and diaphoresis. Neuroleptic malignant syndrome was diagnosed. Supporting treatment was provided and intercurrences treated. Neuroleptic malignant syndrome is a fatal disease in 10 to 20% of patients; otherwise it resolves in about two weeks. In rare cases, like this one the authors report, it has a prolonged evolution of months.
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spelling Neuroleptic malignant syndrome: a rare long lasting case report.Síndrome maligno dos neurolépticos: um caso raro de evolução prolongada.Neuroleptic malignant syndrome (NMS) is a neurological emergency related to neuroleptics medication. Diagnosis is clinical. Authors present the case of a 32-year-old Caucasian man with a history of moderated oligophreny treated with stable doses of psychotropic and neuroleptic drugs. Because of aggressivity outbreaks, he was administered high doses of intramuscular haloperidol decanoate for a period of ten days. One month later he had evolved with mental deterioration, mutism, generalized rigidity, fever, tachycardia, hypotension and diaphoresis. Neuroleptic malignant syndrome was diagnosed. Supporting treatment was provided and intercurrences treated. Neuroleptic malignant syndrome is a fatal disease in 10 to 20% of patients; otherwise it resolves in about two weeks. In rare cases, like this one the authors report, it has a prolonged evolution of months.Neuroleptic malignant syndrome (NMS) is a neurological emergency related to neuroleptics medication. Diagnosis is clinical. Authors present the case of a 32-year-old Caucasian man with a history of moderated oligophreny treated with stable doses of psychotropic and neuroleptic drugs. Because of aggressivity outbreaks, he was administered high doses of intramuscular haloperidol decanoate for a period of ten days. One month later he had evolved with mental deterioration, mutism, generalized rigidity, fever, tachycardia, hypotension and diaphoresis. Neuroleptic malignant syndrome was diagnosed. Supporting treatment was provided and intercurrences treated. Neuroleptic malignant syndrome is a fatal disease in 10 to 20% of patients; otherwise it resolves in about two weeks. In rare cases, like this one the authors report, it has a prolonged evolution of months.Ordem dos Médicos2010-12-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/732oai:ojs.www.actamedicaportuguesa.com:article/732Acta Médica Portuguesa; Vol. 23 No. 6 (2010): November-December; 1155-9Acta Médica Portuguesa; Vol. 23 N.º 6 (2010): Novembro-Dezembro; 1155-91646-07580870-399Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/732https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/732/409Lemos, JoanaMós, MartaMonteiro, AntónioHenriques, Pedroinfo:eu-repo/semantics/openAccess2022-12-20T10:56:49Zoai:ojs.www.actamedicaportuguesa.com:article/732Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:16:43.259701Repositório 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 Neuroleptic malignant syndrome: a rare long lasting case report.
Síndrome maligno dos neurolépticos: um caso raro de evolução prolongada.
title Neuroleptic malignant syndrome: a rare long lasting case report.
spellingShingle Neuroleptic malignant syndrome: a rare long lasting case report.
Lemos, Joana
title_short Neuroleptic malignant syndrome: a rare long lasting case report.
title_full Neuroleptic malignant syndrome: a rare long lasting case report.
title_fullStr Neuroleptic malignant syndrome: a rare long lasting case report.
title_full_unstemmed Neuroleptic malignant syndrome: a rare long lasting case report.
title_sort Neuroleptic malignant syndrome: a rare long lasting case report.
author Lemos, Joana
author_facet Lemos, Joana
Mós, Marta
Monteiro, António
Henriques, Pedro
author_role author
author2 Mós, Marta
Monteiro, António
Henriques, Pedro
author2_role author
author
author
dc.contributor.author.fl_str_mv Lemos, Joana
Mós, Marta
Monteiro, António
Henriques, Pedro
description Neuroleptic malignant syndrome (NMS) is a neurological emergency related to neuroleptics medication. Diagnosis is clinical. Authors present the case of a 32-year-old Caucasian man with a history of moderated oligophreny treated with stable doses of psychotropic and neuroleptic drugs. Because of aggressivity outbreaks, he was administered high doses of intramuscular haloperidol decanoate for a period of ten days. One month later he had evolved with mental deterioration, mutism, generalized rigidity, fever, tachycardia, hypotension and diaphoresis. Neuroleptic malignant syndrome was diagnosed. Supporting treatment was provided and intercurrences treated. Neuroleptic malignant syndrome is a fatal disease in 10 to 20% of patients; otherwise it resolves in about two weeks. In rare cases, like this one the authors report, it has a prolonged evolution of months.
publishDate 2010
dc.date.none.fl_str_mv 2010-12-28
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dc.language.iso.fl_str_mv por
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https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/732/409
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dc.publisher.none.fl_str_mv Ordem dos Médicos
publisher.none.fl_str_mv Ordem dos Médicos
dc.source.none.fl_str_mv Acta Médica Portuguesa; Vol. 23 No. 6 (2010): November-December; 1155-9
Acta Médica Portuguesa; Vol. 23 N.º 6 (2010): Novembro-Dezembro; 1155-9
1646-0758
0870-399X
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