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A case report of Adult-onset Still’s disease as a cause of severe mitral regurgitation
BACKGROUND: Adult-onset Still’s disease (AOSD) is an uncommon systemic inflammatory disease, causing spiking fever, skin rash, and arthritis. Pericarditis and myocarditis are the most common cardiac manifestation of AOSD but valvular involvement is rarely reported. CASE SUMMARY: An 18-year-old boy p...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501920/ https://www.ncbi.nlm.nih.gov/pubmed/32974464 http://dx.doi.org/10.1093/ehjcr/ytaa127 |
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author | Shah, Shabir Hussain Shah, Muhammad Azam Khan, Mohammad Shahbaz Alghamdi, Faisal Abdullah |
author_facet | Shah, Shabir Hussain Shah, Muhammad Azam Khan, Mohammad Shahbaz Alghamdi, Faisal Abdullah |
author_sort | Shah, Shabir Hussain |
collection | PubMed |
description | BACKGROUND: Adult-onset Still’s disease (AOSD) is an uncommon systemic inflammatory disease, causing spiking fever, skin rash, and arthritis. Pericarditis and myocarditis are the most common cardiac manifestation of AOSD but valvular involvement is rarely reported. CASE SUMMARY: An 18-year-old boy presented with gradually worsening shortness of breath for 6 months. There was a history of low-grade intermittent fever and polyarthralgia affecting ankles, knees, and elbows. He was in heart failure with cardiogenic and septic shock. He was managed initially with antibiotics, inotropes, and diuretics. Echocardiography showed flail anterior mitral leaflet with severe mitral regurgitation. He remained febrile with persistent negative blood cultures. Intravenous antibiotics led to neutropenia without any response to fever and clinical status. On further workup, he was diagnosed to have AOSD, and he responded dramatically to oral steroid therapy. Later his mitral valve was replaced surgically. On follow-up, he was stable with mild exertional dyspnoea. His international normalized ratio was in therapeutic range and his follow-up echocardiography showed normally functioning mitral prosthesis. He is following rheumatology and currently on the maintenance dose of steroids. DISCUSSION: Adult-onset Still’s disease is a systemic illness with diagnosis is based on clinical features and exclusion of other illnesses. Adult-onset Still’s disease should be considered as a differential diagnosis in culture-negative endocarditis, especially in those with systemic features and non-responders to antibiotics. |
format | Online Article Text |
id | pubmed-7501920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-75019202020-09-23 A case report of Adult-onset Still’s disease as a cause of severe mitral regurgitation Shah, Shabir Hussain Shah, Muhammad Azam Khan, Mohammad Shahbaz Alghamdi, Faisal Abdullah Eur Heart J Case Rep Case Reports BACKGROUND: Adult-onset Still’s disease (AOSD) is an uncommon systemic inflammatory disease, causing spiking fever, skin rash, and arthritis. Pericarditis and myocarditis are the most common cardiac manifestation of AOSD but valvular involvement is rarely reported. CASE SUMMARY: An 18-year-old boy presented with gradually worsening shortness of breath for 6 months. There was a history of low-grade intermittent fever and polyarthralgia affecting ankles, knees, and elbows. He was in heart failure with cardiogenic and septic shock. He was managed initially with antibiotics, inotropes, and diuretics. Echocardiography showed flail anterior mitral leaflet with severe mitral regurgitation. He remained febrile with persistent negative blood cultures. Intravenous antibiotics led to neutropenia without any response to fever and clinical status. On further workup, he was diagnosed to have AOSD, and he responded dramatically to oral steroid therapy. Later his mitral valve was replaced surgically. On follow-up, he was stable with mild exertional dyspnoea. His international normalized ratio was in therapeutic range and his follow-up echocardiography showed normally functioning mitral prosthesis. He is following rheumatology and currently on the maintenance dose of steroids. DISCUSSION: Adult-onset Still’s disease is a systemic illness with diagnosis is based on clinical features and exclusion of other illnesses. Adult-onset Still’s disease should be considered as a differential diagnosis in culture-negative endocarditis, especially in those with systemic features and non-responders to antibiotics. Oxford University Press 2020-06-17 /pmc/articles/PMC7501920/ /pubmed/32974464 http://dx.doi.org/10.1093/ehjcr/ytaa127 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the European Society of Cardiology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Case Reports Shah, Shabir Hussain Shah, Muhammad Azam Khan, Mohammad Shahbaz Alghamdi, Faisal Abdullah A case report of Adult-onset Still’s disease as a cause of severe mitral regurgitation |
title | A case report of Adult-onset Still’s disease as a cause of severe mitral regurgitation |
title_full | A case report of Adult-onset Still’s disease as a cause of severe mitral regurgitation |
title_fullStr | A case report of Adult-onset Still’s disease as a cause of severe mitral regurgitation |
title_full_unstemmed | A case report of Adult-onset Still’s disease as a cause of severe mitral regurgitation |
title_short | A case report of Adult-onset Still’s disease as a cause of severe mitral regurgitation |
title_sort | case report of adult-onset still’s disease as a cause of severe mitral regurgitation |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501920/ https://www.ncbi.nlm.nih.gov/pubmed/32974464 http://dx.doi.org/10.1093/ehjcr/ytaa127 |
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