Achenbach Syndrome: presentation of a case report and review of the literature

Detalhes bibliográficos
Autor(a) principal: Utiamada, Jéssica Lie
Data de Publicação: 2021
Outros Autores: Cassemiro, Pâmela Mayara da Silva, Brandl, Rafael Cristiano, Davet, Bertha Aparecida, Cunha, João Pedro Pereira da
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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spelling 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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