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Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT Syndrome
Sudden death is defined as the unexpected death of a healthy person that occurs within the first hour of the onset of symptoms or within 24 h of the victim being last seen alive. In some of these cases, rare deleterious variants of genes associated with inherited cardiac disorders can provide a high...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569895/ https://www.ncbi.nlm.nih.gov/pubmed/36232963 http://dx.doi.org/10.3390/ijms231911666 |
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author | Grassi, Simone Campuzano, Oscar Coll, Mònica Cazzato, Francesca Iglesias, Anna Ausania, Francesco Scarnicci, Francesca Sarquella-Brugada, Georgia Brugada, Josep Arena, Vincenzo Oliva, Antonio Brugada, Ramon |
author_facet | Grassi, Simone Campuzano, Oscar Coll, Mònica Cazzato, Francesca Iglesias, Anna Ausania, Francesco Scarnicci, Francesca Sarquella-Brugada, Georgia Brugada, Josep Arena, Vincenzo Oliva, Antonio Brugada, Ramon |
author_sort | Grassi, Simone |
collection | PubMed |
description | Sudden death is defined as the unexpected death of a healthy person that occurs within the first hour of the onset of symptoms or within 24 h of the victim being last seen alive. In some of these cases, rare deleterious variants of genes associated with inherited cardiac disorders can provide a highly probable explanation for the fatal event. We report the case of a 21-year-old obese woman who lost consciousness suddenly in a public place and was pronounced dead after hospital admission. Clinical autopsy showed an inconclusive gross examination, while in the histopathological analysis an eosinophilic inflammatory focus and interstitial fibrosis in the sino-atrial node were found. Molecular autopsy revealed an intronic variant in the KCNQ1 gene (c.683 + 5G > A), classified as likely pathogenic for long QT syndrome according to the guidelines provided by the American College of Medical Genetics and Genomics. Therefore, there were many anomalies that could have played a role in the causation of the sudden death, such as the extreme obesity, the cardiac anomalies and the KNCQ1 variant. This case depicts the difficult interpretation of rare cardiac structural abnormalities in subjects carrying rare variants responsible for inherited arrhythmic disorders and the challenge for the forensic pathologist to make causal inferences in the determinism of the unexpected decease. |
format | Online Article Text |
id | pubmed-9569895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95698952022-10-17 Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT Syndrome Grassi, Simone Campuzano, Oscar Coll, Mònica Cazzato, Francesca Iglesias, Anna Ausania, Francesco Scarnicci, Francesca Sarquella-Brugada, Georgia Brugada, Josep Arena, Vincenzo Oliva, Antonio Brugada, Ramon Int J Mol Sci Case Report Sudden death is defined as the unexpected death of a healthy person that occurs within the first hour of the onset of symptoms or within 24 h of the victim being last seen alive. In some of these cases, rare deleterious variants of genes associated with inherited cardiac disorders can provide a highly probable explanation for the fatal event. We report the case of a 21-year-old obese woman who lost consciousness suddenly in a public place and was pronounced dead after hospital admission. Clinical autopsy showed an inconclusive gross examination, while in the histopathological analysis an eosinophilic inflammatory focus and interstitial fibrosis in the sino-atrial node were found. Molecular autopsy revealed an intronic variant in the KCNQ1 gene (c.683 + 5G > A), classified as likely pathogenic for long QT syndrome according to the guidelines provided by the American College of Medical Genetics and Genomics. Therefore, there were many anomalies that could have played a role in the causation of the sudden death, such as the extreme obesity, the cardiac anomalies and the KNCQ1 variant. This case depicts the difficult interpretation of rare cardiac structural abnormalities in subjects carrying rare variants responsible for inherited arrhythmic disorders and the challenge for the forensic pathologist to make causal inferences in the determinism of the unexpected decease. MDPI 2022-10-01 /pmc/articles/PMC9569895/ /pubmed/36232963 http://dx.doi.org/10.3390/ijms231911666 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Grassi, Simone Campuzano, Oscar Coll, Mònica Cazzato, Francesca Iglesias, Anna Ausania, Francesco Scarnicci, Francesca Sarquella-Brugada, Georgia Brugada, Josep Arena, Vincenzo Oliva, Antonio Brugada, Ramon Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT Syndrome |
title | Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT Syndrome |
title_full | Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT Syndrome |
title_fullStr | Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT Syndrome |
title_full_unstemmed | Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT Syndrome |
title_short | Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT Syndrome |
title_sort | eosinophilic infiltration of the sino-atrial node in sudden cardiac death caused by long qt syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569895/ https://www.ncbi.nlm.nih.gov/pubmed/36232963 http://dx.doi.org/10.3390/ijms231911666 |
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