Hyperpigmentation in Addison’s Disease: Case Report

Detalhes bibliográficos
Autor(a) principal: Figueiredo Gatti, Rafael
Data de Publicação: 2017
Outros Autores: Medeiros Prohmann, Carolina, Araújo Dantas, Camila, Barcelos e Silva, Lorena, Marçal Machado, Thalita, Rodrigues de Oliveira Mattar, Fernanda, Roberto Antônio, João
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.29021/spdv.75.2.772
Resumo: The primary adrenal insufficiency or Addison's disease is a rare disorder of the adrenal glands and is a risk factor, since its diagnosis is often not recognized in the early stages of the disease. Currently, its main cause is idiopathic atrophy, but it can occur due to infectious, traumatic and neoplastic causes. Symptoms of the condition include: asthenia, weakness, nausea, weight loss, hypotension, and hyperpigmentation. The skin and mucosa hyperpigmentation is the most characteristic symptom of the disease, but may be present in other differential diagnoses, such as hemochromatosis, chronic kidney disease, hyperthyroidism, ocronosis, among others. We report a case of a patient who was referred for investigation of diffuse cutaneous and mucosa hyperpigmentation. The patient also indicated complaints of weight loss, fatigue, anorexia, hypotension and constipation. Several tests were conducted to research and accomplished the diagnosis of Addison's disease.
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spelling Hyperpigmentation in Addison’s Disease: Case ReportHiperpigmentação na Doença de Addison: Relato de CasoAddison DiseaseHyperpigmentationDoença de AddisonHiperpigmentaçãoThe primary adrenal insufficiency or Addison's disease is a rare disorder of the adrenal glands and is a risk factor, since its diagnosis is often not recognized in the early stages of the disease. Currently, its main cause is idiopathic atrophy, but it can occur due to infectious, traumatic and neoplastic causes. Symptoms of the condition include: asthenia, weakness, nausea, weight loss, hypotension, and hyperpigmentation. The skin and mucosa hyperpigmentation is the most characteristic symptom of the disease, but may be present in other differential diagnoses, such as hemochromatosis, chronic kidney disease, hyperthyroidism, ocronosis, among others. We report a case of a patient who was referred for investigation of diffuse cutaneous and mucosa hyperpigmentation. The patient also indicated complaints of weight loss, fatigue, anorexia, hypotension and constipation. Several tests were conducted to research and accomplished the diagnosis of Addison's disease.A insuficiência adrenal primária ou doença de Addison é um raro distúrbio das glândulas supra-renais e representa uma condição de risco, já que seu diagnóstico é frequentemente não reconhecido nas fases inicias da doença. Atualmente sua principal causa é a atrofia idiopática, mas pode decorrer devido a causas infecciosas, traumáticas e neoplásicas. Os sintomas da patologia incluem: astenia, náuseas, perda de peso, hipotensão arterial e hiperpigmentação. A hiperpigmentação cutânea e mucosa é o sinal mais característico da doença, porém pode estar presente em outros diagnósticos diferencias, como: hemocromatose, doença renal crônica, hipertireoidismo, ocronose, entre outras. Relatamos um caso de uma paciente que foi encaminhada para investigação de hiperpigmentação cutânea difusa e mucosa. A paciente ainda referia queixas de perda de peso, fadiga, anorexia, hipotensão e obstipação. Foram realizados diversos exames para investigação e realizado o diagnóstico de doença de Addison.Sociedade Portuguesa de Dermatologia e Venereologia2017-07-20T00:00:00Zjournal articleinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://doi.org/10.29021/spdv.75.2.772oai:ojs.revista.spdv.com.pt:article/772Journal of the Portuguese Society of Dermatology and Venereology; Vol 75 No 2 (2017): Abril - Junho; 169-172Revista da Sociedade Portuguesa de Dermatologia e Venereologia; v. 75 n. 2 (2017): Abril - Junho; 169-1722182-24092182-2395reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://revista.spdv.com.pt/index.php/spdv/article/view/772https://doi.org/10.29021/spdv.75.2.772https://revista.spdv.com.pt/index.php/spdv/article/view/772/496Figueiredo Gatti, RafaelMedeiros Prohmann, CarolinaAraújo Dantas, CamilaBarcelos e Silva, LorenaMarçal Machado, ThalitaRodrigues de Oliveira Mattar, FernandaRoberto Antônio, Joãoinfo:eu-repo/semantics/openAccess2022-10-06T12:35:03Zoai:ojs.revista.spdv.com.pt:article/772Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:11:02.528908Repositório 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 Hyperpigmentation in Addison’s Disease: Case Report
Hiperpigmentação na Doença de Addison: Relato de Caso
title Hyperpigmentation in Addison’s Disease: Case Report
spellingShingle Hyperpigmentation in Addison’s Disease: Case Report
Figueiredo Gatti, Rafael
Addison Disease
Hyperpigmentation
Doença de Addison
Hiperpigmentação
title_short Hyperpigmentation in Addison’s Disease: Case Report
title_full Hyperpigmentation in Addison’s Disease: Case Report
title_fullStr Hyperpigmentation in Addison’s Disease: Case Report
title_full_unstemmed Hyperpigmentation in Addison’s Disease: Case Report
title_sort Hyperpigmentation in Addison’s Disease: Case Report
author Figueiredo Gatti, Rafael
author_facet Figueiredo Gatti, Rafael
Medeiros Prohmann, Carolina
Araújo Dantas, Camila
Barcelos e Silva, Lorena
Marçal Machado, Thalita
Rodrigues de Oliveira Mattar, Fernanda
Roberto Antônio, João
author_role author
author2 Medeiros Prohmann, Carolina
Araújo Dantas, Camila
Barcelos e Silva, Lorena
Marçal Machado, Thalita
Rodrigues de Oliveira Mattar, Fernanda
Roberto Antônio, João
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Figueiredo Gatti, Rafael
Medeiros Prohmann, Carolina
Araújo Dantas, Camila
Barcelos e Silva, Lorena
Marçal Machado, Thalita
Rodrigues de Oliveira Mattar, Fernanda
Roberto Antônio, João
dc.subject.por.fl_str_mv Addison Disease
Hyperpigmentation
Doença de Addison
Hiperpigmentação
topic Addison Disease
Hyperpigmentation
Doença de Addison
Hiperpigmentação
description The primary adrenal insufficiency or Addison's disease is a rare disorder of the adrenal glands and is a risk factor, since its diagnosis is often not recognized in the early stages of the disease. Currently, its main cause is idiopathic atrophy, but it can occur due to infectious, traumatic and neoplastic causes. Symptoms of the condition include: asthenia, weakness, nausea, weight loss, hypotension, and hyperpigmentation. The skin and mucosa hyperpigmentation is the most characteristic symptom of the disease, but may be present in other differential diagnoses, such as hemochromatosis, chronic kidney disease, hyperthyroidism, ocronosis, among others. We report a case of a patient who was referred for investigation of diffuse cutaneous and mucosa hyperpigmentation. The patient also indicated complaints of weight loss, fatigue, anorexia, hypotension and constipation. Several tests were conducted to research and accomplished the diagnosis of Addison's disease.
publishDate 2017
dc.date.none.fl_str_mv 2017-07-20T00:00:00Z
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dc.identifier.uri.fl_str_mv https://doi.org/10.29021/spdv.75.2.772
oai:ojs.revista.spdv.com.pt:article/772
url https://doi.org/10.29021/spdv.75.2.772
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dc.relation.none.fl_str_mv https://revista.spdv.com.pt/index.php/spdv/article/view/772
https://doi.org/10.29021/spdv.75.2.772
https://revista.spdv.com.pt/index.php/spdv/article/view/772/496
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dc.publisher.none.fl_str_mv Sociedade Portuguesa de Dermatologia e Venereologia
publisher.none.fl_str_mv Sociedade Portuguesa de Dermatologia e Venereologia
dc.source.none.fl_str_mv Journal of the Portuguese Society of Dermatology and Venereology; Vol 75 No 2 (2017): Abril - Junho; 169-172
Revista da Sociedade Portuguesa de Dermatologia e Venereologia; v. 75 n. 2 (2017): Abril - Junho; 169-172
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