Achenbach Syndrome: presentation of a case report and review of the literature
Autor(a) principal: | |
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Data de Publicação: | 2021 |
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/19672 |
Resumo: | The objective of this work is to describe a case report of an adult patient whit a previous diagnosis of a autoimmune disease. Better understanding of the clinical picture and medical actions performed. The patient sought care in the city of Lages on 10/09/2019, due to a complaint of changes in hand color, beginning 4 months ago, persisting for 4 hours. No fingings of clinical significance on physical examination. During outpatient investigation, laboratory tests and arterial Doppler of the upper limbs were performed, without evidence of vasculopathy, hematological diseases or other pathologies. After excluding other diseases, Achenbach’s Syndrome became the most likely one. Due to the favorable evolution of this pathology, some medications had been prescribed for the patient’s symptomatic improvement and requests for exames to reassess the condition in 6 months. Thus, it is concluded that Achenbach’s syndrome is configured as a complex pathology, since its etiology and pathophysiology are not well defined, causing difficulty in making the diagnosis of this little-known entity. |
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Achenbach Syndrome: presentation of a case report and review of the literature Síndrome de Achenbach: presentación de un caso clínico y revisión de la literatura Síndrome de Achenbach: apresentação de um relato de caso e revisão de literatura Síndrome de AchenbachHematoma nas extremidadesCianose. Síndrome de AchenbachHematoma en las extremidadesCianosis. Achenbach SyndromeHematoma in the extremitiesCyanosis. The objective of this work is to describe a case report of an adult patient whit a previous diagnosis of a autoimmune disease. Better understanding of the clinical picture and medical actions performed. The patient sought care in the city of Lages on 10/09/2019, due to a complaint of changes in hand color, beginning 4 months ago, persisting for 4 hours. No fingings of clinical significance on physical examination. During outpatient investigation, laboratory tests and arterial Doppler of the upper limbs were performed, without evidence of vasculopathy, hematological diseases or other pathologies. After excluding other diseases, Achenbach’s Syndrome became the most likely one. Due to the favorable evolution of this pathology, some medications had been prescribed for the patient’s symptomatic improvement and requests for exames to reassess the condition in 6 months. Thus, it is concluded that Achenbach’s syndrome is configured as a complex pathology, since its etiology and pathophysiology are not well defined, causing difficulty in making the diagnosis of this little-known entity.El objetivo de este trabajo es describir un reporte de caso de un paciente adulto con diagnóstico previo de una efermedad autoinmune. Se configura como un estudio de reporte de caso clínico mediante la recolección directa de datos del paciente, describiendo los eventos de forma cronológica, con el objetivo en una mejor comprensión del cuadro clínico y las acciones médicas realizadas. El paciente buscó atención en la ciudad de Lages el 09/20/2019, debido a una queja de cambios en el color de la mano, iniciada hace 4 meses, persistiendo durante 4 horas. No hay hallazgos de importancia clínica en la expliración física. Durante la investigación ambulatoria, se realizaron pruebas de laboratory y Doppler arterial de miembros superiores, sin evidencia de vasculopatía, enfermedades hematológicas u outras patologías. Después de excluir otras efermedades, el Síndrome de Achenbach se convirtió en el más probable, debido a la evolución favorable de esta patología, se prescribieron algunos medicamentos para la mejoría sintomática del paciente y se solicitaron pruebas para reevaluar la condición en el plazo de 6 meses. Así, se concluy el Síndrome de Achenbach se configura como una patología compleja, ua que su etiología y fisiopatología no están bien defínidas, lo que dificulta el diagnóstico de esta entidad poco conocida. O objetivo deste trabalho é descrever um relato de caso de um paciente adulto com diagnóstico prévio de uma doença autoimune. Configura-se como estudo do tipo relato de caso clínico por meio de coleta direta dos dados do paciente, descrevendo os acontecimentos de forma cronológica, visando o melhor entendimento do quadro clínico e ações médicas realizadas. A paciente procurou atendimento na cidade de Lages no dia 09/10/2019, devido a uma queixa de alteração em coloração de mãos, de início há 4 meses, persistindo por 4 horas. Sem achados de significância clínica em exame físico. Durante investigação ambulatorial fora realizados exames laboratoriais e Doppler arterial de membros superiores, sem evidência de vasculopatia, doenças hematológicas ou outras patologias. Após exclusão de demais doenças a Síndrome de Achenbach tornou-se a de maior probabilidade. Devido a evolução favorável dessa patologia, fora prescrito alguns medicamentos para melhora sintomática de paciente e solicitação de exames para reavaliação de quadro em 6 meses. Desta forma conclui-se que a síndrome de Achenbach configura-se como uma patologia complexa, uma vez que sua etiologia e fisiopatologia não são bem definidas, gerando dificuldade na realização de diagnóstico dessa entidade pouco conhecida.Research, Society and Development2021-09-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/1967210.33448/rsd-v10i11.19672Research, Society and Development; Vol. 10 No. 11; e573101119672Research, Society and Development; Vol. 10 Núm. 11; e573101119672Research, Society and Development; v. 10 n. 11; e5731011196722525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/19672/17869Copyright (c) 2021 Jéssica Lie Utiamada; Pâmela Mayara da Silva Cassemiro; Rafael Cristiano Brandl; Bertha Aparecida Davet; João Pedro Pereira da Cunhahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessUtiamada, Jéssica LieCassemiro, Pâmela Mayara da Silva Brandl, Rafael Cristiano Davet, Bertha Aparecida Cunha, João Pedro Pereira da 2021-10-23T19:01:11Zoai:ojs.pkp.sfu.ca:article/19672Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:39:31.917212Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
Achenbach Syndrome: presentation of a case report and review of the literature Síndrome de Achenbach: presentación de un caso clínico y revisión de la literatura Síndrome de Achenbach: apresentação de um relato de caso e revisão de literatura |
title |
Achenbach Syndrome: presentation of a case report and review of the literature |
spellingShingle |
Achenbach Syndrome: presentation of a case report and review of the literature Utiamada, Jéssica Lie Síndrome de Achenbach Hematoma nas extremidades Cianose. Síndrome de Achenbach Hematoma en las extremidades Cianosis. Achenbach Syndrome Hematoma in the extremities Cyanosis. |
title_short |
Achenbach Syndrome: presentation of a case report and review of the literature |
title_full |
Achenbach Syndrome: presentation of a case report and review of the literature |
title_fullStr |
Achenbach Syndrome: presentation of a case report and review of the literature |
title_full_unstemmed |
Achenbach Syndrome: presentation of a case report and review of the literature |
title_sort |
Achenbach Syndrome: presentation of a case report and review of the literature |
author |
Utiamada, Jéssica Lie |
author_facet |
Utiamada, Jéssica Lie Cassemiro, Pâmela Mayara da Silva Brandl, Rafael Cristiano Davet, Bertha Aparecida Cunha, João Pedro Pereira da |
author_role |
author |
author2 |
Cassemiro, Pâmela Mayara da Silva Brandl, Rafael Cristiano Davet, Bertha Aparecida Cunha, João Pedro Pereira da |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Utiamada, Jéssica Lie Cassemiro, Pâmela Mayara da Silva Brandl, Rafael Cristiano Davet, Bertha Aparecida Cunha, João Pedro Pereira da |
dc.subject.por.fl_str_mv |
Síndrome de Achenbach Hematoma nas extremidades Cianose. Síndrome de Achenbach Hematoma en las extremidades Cianosis. Achenbach Syndrome Hematoma in the extremities Cyanosis. |
topic |
Síndrome de Achenbach Hematoma nas extremidades Cianose. Síndrome de Achenbach Hematoma en las extremidades Cianosis. Achenbach Syndrome Hematoma in the extremities Cyanosis. |
description |
The objective of this work is to describe a case report of an adult patient whit a previous diagnosis of a autoimmune disease. Better understanding of the clinical picture and medical actions performed. The patient sought care in the city of Lages on 10/09/2019, due to a complaint of changes in hand color, beginning 4 months ago, persisting for 4 hours. No fingings of clinical significance on physical examination. During outpatient investigation, laboratory tests and arterial Doppler of the upper limbs were performed, without evidence of vasculopathy, hematological diseases or other pathologies. After excluding other diseases, Achenbach’s Syndrome became the most likely one. Due to the favorable evolution of this pathology, some medications had been prescribed for the patient’s symptomatic improvement and requests for exames to reassess the condition in 6 months. Thus, it is concluded that Achenbach’s syndrome is configured as a complex pathology, since its etiology and pathophysiology are not well defined, causing difficulty in making the diagnosis of this little-known entity. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-09-11 |
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/19672 10.33448/rsd-v10i11.19672 |
url |
https://rsdjournal.org/index.php/rsd/article/view/19672 |
identifier_str_mv |
10.33448/rsd-v10i11.19672 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/19672/17869 |
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. 10 No. 11; e573101119672 Research, Society and Development; Vol. 10 Núm. 11; e573101119672 Research, Society and Development; v. 10 n. 11; e573101119672 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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1797052688212426752 |