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Kounis Syndrome Induced by Anisodamine: A Case Report

Kounis syndrome is a rare type of acute coronary syndrome caused by coronary spasm with or without atherosclerotic plaque erosion or rupture due to inflammatory factors released by allergic reactions. Due to a lack of awareness, Kounis syndrome is often underdiagnosed. Here, we for the first time re...

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Autores principales: Wu, Haoyu, Cao, Yiwei, Chang, Fengjun, Zhang, Chunyan, Hu, Yanchao, Liang, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754087/
https://www.ncbi.nlm.nih.gov/pubmed/33363401
http://dx.doi.org/10.2147/IJGM.S289015
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author Wu, Haoyu
Cao, Yiwei
Chang, Fengjun
Zhang, Chunyan
Hu, Yanchao
Liang, Lei
author_facet Wu, Haoyu
Cao, Yiwei
Chang, Fengjun
Zhang, Chunyan
Hu, Yanchao
Liang, Lei
author_sort Wu, Haoyu
collection PubMed
description Kounis syndrome is a rare type of acute coronary syndrome caused by coronary spasm with or without atherosclerotic plaque erosion or rupture due to inflammatory factors released by allergic reactions. Due to a lack of awareness, Kounis syndrome is often underdiagnosed. Here, we for the first time report a case of Kounis syndrome induced by anisodamine. A 48-year-old woman presented with upper abdominal pain and vomiting after eating. She was diagnosed with gastrointestinal spasm and intramuscularly injected with 10 mg anisodamine. The patient subsequently developed chest pain and hypotension with erythematous rash. A systemic allergic reaction was diagnosed. Saline solution, promethazine and dexamethasone were administered immediately. A 12-lead electrocardiogram indicated ST-segment elevation in II, III and aVF leads. Emergent coronary angiography was recommended. According to a preoperative electrocardiogram, the ST-segment elevation in the II, III and aVF leads had disappeared. Coronary angiograph revealed no significant coronary stenosis. The patient was diagnosed with Kounis syndrome induced by anisodamine, showing acute ST-segment elevation myocardial infarction due to allergic coronary vasospasm. During the 9-month follow-up, the patient did not receive further anisodamine injections and remained free of chest pain. In conclusion, it is essential for clinicians to be aware of Kounis syndrome because of the wide range of triggers and its potentially fatal evolution if not identified in time.
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spelling pubmed-77540872020-12-23 Kounis Syndrome Induced by Anisodamine: A Case Report Wu, Haoyu Cao, Yiwei Chang, Fengjun Zhang, Chunyan Hu, Yanchao Liang, Lei Int J Gen Med Case Report Kounis syndrome is a rare type of acute coronary syndrome caused by coronary spasm with or without atherosclerotic plaque erosion or rupture due to inflammatory factors released by allergic reactions. Due to a lack of awareness, Kounis syndrome is often underdiagnosed. Here, we for the first time report a case of Kounis syndrome induced by anisodamine. A 48-year-old woman presented with upper abdominal pain and vomiting after eating. She was diagnosed with gastrointestinal spasm and intramuscularly injected with 10 mg anisodamine. The patient subsequently developed chest pain and hypotension with erythematous rash. A systemic allergic reaction was diagnosed. Saline solution, promethazine and dexamethasone were administered immediately. A 12-lead electrocardiogram indicated ST-segment elevation in II, III and aVF leads. Emergent coronary angiography was recommended. According to a preoperative electrocardiogram, the ST-segment elevation in the II, III and aVF leads had disappeared. Coronary angiograph revealed no significant coronary stenosis. The patient was diagnosed with Kounis syndrome induced by anisodamine, showing acute ST-segment elevation myocardial infarction due to allergic coronary vasospasm. During the 9-month follow-up, the patient did not receive further anisodamine injections and remained free of chest pain. In conclusion, it is essential for clinicians to be aware of Kounis syndrome because of the wide range of triggers and its potentially fatal evolution if not identified in time. Dove 2020-12-14 /pmc/articles/PMC7754087/ /pubmed/33363401 http://dx.doi.org/10.2147/IJGM.S289015 Text en © 2020 Wu et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Case Report
Wu, Haoyu
Cao, Yiwei
Chang, Fengjun
Zhang, Chunyan
Hu, Yanchao
Liang, Lei
Kounis Syndrome Induced by Anisodamine: A Case Report
title Kounis Syndrome Induced by Anisodamine: A Case Report
title_full Kounis Syndrome Induced by Anisodamine: A Case Report
title_fullStr Kounis Syndrome Induced by Anisodamine: A Case Report
title_full_unstemmed Kounis Syndrome Induced by Anisodamine: A Case Report
title_short Kounis Syndrome Induced by Anisodamine: A Case Report
title_sort kounis syndrome induced by anisodamine: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754087/
https://www.ncbi.nlm.nih.gov/pubmed/33363401
http://dx.doi.org/10.2147/IJGM.S289015
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