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Think twice – Diagnostic delay in a patient with acute chest pain

Heart involvement is the most critical and potentially lethal systemic manifestation in eosinophilic granulomatosis with polyangiitis (EGPA). We present a case of acute chest pain in a 58-year-old male with severe asthma, which regressed after sublingual administration of nitroglycerine. At the time...

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Autores principales: Bang, Cæcilie Larsen, Porsbjerg, Celeste Michala
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011159/
https://www.ncbi.nlm.nih.gov/pubmed/27625985
http://dx.doi.org/10.1016/j.rmcr.2016.08.004
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author Bang, Cæcilie Larsen
Porsbjerg, Celeste Michala
author_facet Bang, Cæcilie Larsen
Porsbjerg, Celeste Michala
author_sort Bang, Cæcilie Larsen
collection PubMed
description Heart involvement is the most critical and potentially lethal systemic manifestation in eosinophilic granulomatosis with polyangiitis (EGPA). We present a case of acute chest pain in a 58-year-old male with severe asthma, which regressed after sublingual administration of nitroglycerine. At the time of hospital admission, there were non-specific ST-changes on the ecg, coronary enzymes were increased, and the patient was concluded to have a non-ST-elevation myocardial infarction, and treated as such. A subacute cardiac catheterization showed no signs of significant coronary stenosis. During the next days, there was increasing pain and reduced strength in both feet. Paraclinical imaging and neurological examinations could not explain the symptoms, and physiotherapy was initiated. At the time, no connection to patient's diagnosis of severe asthma was made. The patient was seen in the respiratory outpatient clinic for a routine check-up, three weeks after the initial hospital admission. At this point, there was increasing pain in both legs and the patient had difficulty walking and experienced increasing dyspnea. Blood eosinophils were elevated (12.7 × 10(9)/L), and an acute HRCT scan showed bilateral peribronchial infiltrates with ground glass opacification and small noduli. A diagnosis of EGPA was established, and administration of systemic glucocorticoids was initiated. A year and a half later, there is still reduced strength and sensory loss. This case illustrates that it is important to consider alternative diagnoses in patients with atypical symptoms and a low risk profile. Heart involvement is the most critical and potentially lethal systemic manifestation in eosinophilic granulomatosis with polyangiitis (EGPA, formerly known as Churg-Strauss syndrome), which makes a quick diagnosis and prompt initiation of correct treatment imperative.
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spelling pubmed-50111592016-09-13 Think twice – Diagnostic delay in a patient with acute chest pain Bang, Cæcilie Larsen Porsbjerg, Celeste Michala Respir Med Case Rep Case Report Heart involvement is the most critical and potentially lethal systemic manifestation in eosinophilic granulomatosis with polyangiitis (EGPA). We present a case of acute chest pain in a 58-year-old male with severe asthma, which regressed after sublingual administration of nitroglycerine. At the time of hospital admission, there were non-specific ST-changes on the ecg, coronary enzymes were increased, and the patient was concluded to have a non-ST-elevation myocardial infarction, and treated as such. A subacute cardiac catheterization showed no signs of significant coronary stenosis. During the next days, there was increasing pain and reduced strength in both feet. Paraclinical imaging and neurological examinations could not explain the symptoms, and physiotherapy was initiated. At the time, no connection to patient's diagnosis of severe asthma was made. The patient was seen in the respiratory outpatient clinic for a routine check-up, three weeks after the initial hospital admission. At this point, there was increasing pain in both legs and the patient had difficulty walking and experienced increasing dyspnea. Blood eosinophils were elevated (12.7 × 10(9)/L), and an acute HRCT scan showed bilateral peribronchial infiltrates with ground glass opacification and small noduli. A diagnosis of EGPA was established, and administration of systemic glucocorticoids was initiated. A year and a half later, there is still reduced strength and sensory loss. This case illustrates that it is important to consider alternative diagnoses in patients with atypical symptoms and a low risk profile. Heart involvement is the most critical and potentially lethal systemic manifestation in eosinophilic granulomatosis with polyangiitis (EGPA, formerly known as Churg-Strauss syndrome), which makes a quick diagnosis and prompt initiation of correct treatment imperative. Elsevier 2016-08-20 /pmc/articles/PMC5011159/ /pubmed/27625985 http://dx.doi.org/10.1016/j.rmcr.2016.08.004 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Bang, Cæcilie Larsen
Porsbjerg, Celeste Michala
Think twice – Diagnostic delay in a patient with acute chest pain
title Think twice – Diagnostic delay in a patient with acute chest pain
title_full Think twice – Diagnostic delay in a patient with acute chest pain
title_fullStr Think twice – Diagnostic delay in a patient with acute chest pain
title_full_unstemmed Think twice – Diagnostic delay in a patient with acute chest pain
title_short Think twice – Diagnostic delay in a patient with acute chest pain
title_sort think twice – diagnostic delay in a patient with acute chest pain
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011159/
https://www.ncbi.nlm.nih.gov/pubmed/27625985
http://dx.doi.org/10.1016/j.rmcr.2016.08.004
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