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Yamaguchi Syndrome: A Hidden Masquerader of Ischemic Heart Disease
Yamaguchi syndrome, also known as apical (Ap) hypertrophic cardiomyopathy (HCM), is a variant of cardiomyopathy that affects the apical region of the left ventricle. ApHCM is frequently misdiagnosed or missed because its symptoms are extremely similar to those of acute coronary syndrome. As clinicia...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9337995/ https://www.ncbi.nlm.nih.gov/pubmed/35915685 http://dx.doi.org/10.7759/cureus.26439 |
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author | Giri, Anamika Acharya, Sourya Kamat, Sandeep Shukla, Samarth Kumar, Sunil |
author_facet | Giri, Anamika Acharya, Sourya Kamat, Sandeep Shukla, Samarth Kumar, Sunil |
author_sort | Giri, Anamika |
collection | PubMed |
description | Yamaguchi syndrome, also known as apical (Ap) hypertrophic cardiomyopathy (HCM), is a variant of cardiomyopathy that affects the apical region of the left ventricle. ApHCM is frequently misdiagnosed or missed because its symptoms are extremely similar to those of acute coronary syndrome. As clinicians are unfamiliar with this disease, diagnosis can be missed or delayed; as a result, this condition is frequently discovered by chance. ApHCM has a favorable long-term prognosis once properly diagnosed. We report a case of a 50-year-old male who was diagnosed with Yamaguchi syndrome incidentally. |
format | Online Article Text |
id | pubmed-9337995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-93379952022-07-31 Yamaguchi Syndrome: A Hidden Masquerader of Ischemic Heart Disease Giri, Anamika Acharya, Sourya Kamat, Sandeep Shukla, Samarth Kumar, Sunil Cureus Cardiology Yamaguchi syndrome, also known as apical (Ap) hypertrophic cardiomyopathy (HCM), is a variant of cardiomyopathy that affects the apical region of the left ventricle. ApHCM is frequently misdiagnosed or missed because its symptoms are extremely similar to those of acute coronary syndrome. As clinicians are unfamiliar with this disease, diagnosis can be missed or delayed; as a result, this condition is frequently discovered by chance. ApHCM has a favorable long-term prognosis once properly diagnosed. We report a case of a 50-year-old male who was diagnosed with Yamaguchi syndrome incidentally. Cureus 2022-06-29 /pmc/articles/PMC9337995/ /pubmed/35915685 http://dx.doi.org/10.7759/cureus.26439 Text en Copyright © 2022, Giri et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Cardiology Giri, Anamika Acharya, Sourya Kamat, Sandeep Shukla, Samarth Kumar, Sunil Yamaguchi Syndrome: A Hidden Masquerader of Ischemic Heart Disease |
title | Yamaguchi Syndrome: A Hidden Masquerader of Ischemic Heart Disease |
title_full | Yamaguchi Syndrome: A Hidden Masquerader of Ischemic Heart Disease |
title_fullStr | Yamaguchi Syndrome: A Hidden Masquerader of Ischemic Heart Disease |
title_full_unstemmed | Yamaguchi Syndrome: A Hidden Masquerader of Ischemic Heart Disease |
title_short | Yamaguchi Syndrome: A Hidden Masquerader of Ischemic Heart Disease |
title_sort | yamaguchi syndrome: a hidden masquerader of ischemic heart disease |
topic | Cardiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9337995/ https://www.ncbi.nlm.nih.gov/pubmed/35915685 http://dx.doi.org/10.7759/cureus.26439 |
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