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Incidental cerebral aneurysm after takotsubo cardiomyopathy: A case report
Takotsubo syndrome (TS) is an acute heart disease that mimics the typical features of acute coronary syndrome (ACS). TS is generally reported after subarachnoid hemorrhage (SAH) due to a ruptured aneurysm, and has an incidence rate of 0.8 (17%). Here, we report a rare case of TS with unruptured intr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547853/ https://www.ncbi.nlm.nih.gov/pubmed/37799569 http://dx.doi.org/10.1002/ccr3.7998 |
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author | Amaro, Tânia Sgarbi, Taynara Vieira, Raísa Santos, Rafael Reis Matos, Priscila Oliveira, Adilson |
author_facet | Amaro, Tânia Sgarbi, Taynara Vieira, Raísa Santos, Rafael Reis Matos, Priscila Oliveira, Adilson |
author_sort | Amaro, Tânia |
collection | PubMed |
description | Takotsubo syndrome (TS) is an acute heart disease that mimics the typical features of acute coronary syndrome (ACS). TS is generally reported after subarachnoid hemorrhage (SAH) due to a ruptured aneurysm, and has an incidence rate of 0.8 (17%). Here, we report a rare case of TS with unruptured intracranial aneurism. A 54‐year‐old woman had a history of systemic arterial hypertension and migraine. She went to a secondary hospital 2 h after sudden‐onset chest pain, which irradiated to the left upper limb and back. The initial electrocardiogram (ECG) was normal but showed a troponin curve, which led us to suspect acute non‐ST elevation myocardial infarction. Serial ECG showed dynamic changes in ST‐segment elevation in DIII, AvF, V5, and V6. Emergency cardiac catheterisation was performed and did not show any obstructive lesions. However, ventriculography revealed hypokinesia of the inferoapical wall. During hospitalization, the patient had a severe refractory headache. Computed tomography (CT) and CT angiography were performed, which identified “mirror” saccular aneurysms. A supraclinoid internal carotid artery aneurysm was embolized with two stents. The patient's condition progressed satisfactorily. The association between takotsubo syndrome and aneurysmal SAH with some populations has already been reported. Due to this prior knowledge, and severe headache, it was necessary to perform screening for SAH and the discovery of an unruptured aneurysm in this case report. The present case report differs from most reported cases of takotsubo syndrome described in the literature because it presents unruptured mirror aneurysms, while most cases are diagnosed after intracranial hemorrhage. |
format | Online Article Text |
id | pubmed-10547853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105478532023-10-05 Incidental cerebral aneurysm after takotsubo cardiomyopathy: A case report Amaro, Tânia Sgarbi, Taynara Vieira, Raísa Santos, Rafael Reis Matos, Priscila Oliveira, Adilson Clin Case Rep Case Report Takotsubo syndrome (TS) is an acute heart disease that mimics the typical features of acute coronary syndrome (ACS). TS is generally reported after subarachnoid hemorrhage (SAH) due to a ruptured aneurysm, and has an incidence rate of 0.8 (17%). Here, we report a rare case of TS with unruptured intracranial aneurism. A 54‐year‐old woman had a history of systemic arterial hypertension and migraine. She went to a secondary hospital 2 h after sudden‐onset chest pain, which irradiated to the left upper limb and back. The initial electrocardiogram (ECG) was normal but showed a troponin curve, which led us to suspect acute non‐ST elevation myocardial infarction. Serial ECG showed dynamic changes in ST‐segment elevation in DIII, AvF, V5, and V6. Emergency cardiac catheterisation was performed and did not show any obstructive lesions. However, ventriculography revealed hypokinesia of the inferoapical wall. During hospitalization, the patient had a severe refractory headache. Computed tomography (CT) and CT angiography were performed, which identified “mirror” saccular aneurysms. A supraclinoid internal carotid artery aneurysm was embolized with two stents. The patient's condition progressed satisfactorily. The association between takotsubo syndrome and aneurysmal SAH with some populations has already been reported. Due to this prior knowledge, and severe headache, it was necessary to perform screening for SAH and the discovery of an unruptured aneurysm in this case report. The present case report differs from most reported cases of takotsubo syndrome described in the literature because it presents unruptured mirror aneurysms, while most cases are diagnosed after intracranial hemorrhage. John Wiley and Sons Inc. 2023-10-03 /pmc/articles/PMC10547853/ /pubmed/37799569 http://dx.doi.org/10.1002/ccr3.7998 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Case Report Amaro, Tânia Sgarbi, Taynara Vieira, Raísa Santos, Rafael Reis Matos, Priscila Oliveira, Adilson Incidental cerebral aneurysm after takotsubo cardiomyopathy: A case report |
title | Incidental cerebral aneurysm after takotsubo cardiomyopathy: A case report |
title_full | Incidental cerebral aneurysm after takotsubo cardiomyopathy: A case report |
title_fullStr | Incidental cerebral aneurysm after takotsubo cardiomyopathy: A case report |
title_full_unstemmed | Incidental cerebral aneurysm after takotsubo cardiomyopathy: A case report |
title_short | Incidental cerebral aneurysm after takotsubo cardiomyopathy: A case report |
title_sort | incidental cerebral aneurysm after takotsubo cardiomyopathy: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547853/ https://www.ncbi.nlm.nih.gov/pubmed/37799569 http://dx.doi.org/10.1002/ccr3.7998 |
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