Noncompaction and Takotsubo Syndrome in a Neuromuscular Disorder
Background. Takotsubo syndrome (TTS) in patients with left ventricular hypertrabeculation/noncompaction (LVHT) has been reported in four patients, and a TTS plus LVHT plus a neuromuscular disorder (NMD) was only reported once so far. Here, we present the fifth patient with LVHT and TTS and the secon...
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doaj-2e3da94688394f4d847de28bd30cb76c2020-11-25T01:05:18ZengHindawi LimitedCase Reports in Cardiology2090-64042090-64122019-01-01201910.1155/2019/69027516902751Noncompaction and Takotsubo Syndrome in a Neuromuscular DisorderJosef Finsterer0Claudia Stöllberger1Walter Benedikt Winkler2Krankenanstalt Rudolfstiftung, Vienna, Austria2nd Medical Department with Cardiology and Intensive Care Medicine, Krankenanstalt Rudolfstiftung, Vienna, Austria2nd Medical Department with Cardiology and Intensive Care Medicine, Krankenanstalt Rudolfstiftung, Vienna, AustriaBackground. Takotsubo syndrome (TTS) in patients with left ventricular hypertrabeculation/noncompaction (LVHT) has been reported in four patients, and a TTS plus LVHT plus a neuromuscular disorder (NMD) was only reported once so far. Here, we present the fifth patient with LVHT and TTS and the second patient with LVHT, TTS, and a NMD. Methods and Results. The patient is a 68 yo female hobby choir singer with a history of skin dermatofibroma, skin fibrokeratoma, arterial hypertension, hyperlipidemia, hypothyroidism, anemia, hyponatremia, diverticulosis, LVHT detected at age 60 y, five syncopes, a liver cyst, and carotid endarterectomy 2 months prior to admission because of sudden-onset chest pain. Workup revealed ST elevation, troponin elevation, and mild coronary artery sclerosis. Ventriculography and transthoracic echocardiography (TTE) showed the apical type of a TTS. ECG normalised within 10 w and TTE within 6 w under beta-blockers and ATII-blockers. The TTS was triggered by being offended of being unable to sing anymore after endarterectomy. Neurological workup suggested the presence of a NMD. Conclusions. This case shows that LVHT occurs in NMD patients and that patients with LVHT and a NMD may develop a TTS. Whether patients with LVHT and a NMD are particularly prone to develop a TTS requires further confirmation. NMD patients with LVHT should avoid stress not to trigger a TTS.http://dx.doi.org/10.1155/2019/6902751 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Josef Finsterer Claudia Stöllberger Walter Benedikt Winkler |
spellingShingle |
Josef Finsterer Claudia Stöllberger Walter Benedikt Winkler Noncompaction and Takotsubo Syndrome in a Neuromuscular Disorder Case Reports in Cardiology |
author_facet |
Josef Finsterer Claudia Stöllberger Walter Benedikt Winkler |
author_sort |
Josef Finsterer |
title |
Noncompaction and Takotsubo Syndrome in a Neuromuscular Disorder |
title_short |
Noncompaction and Takotsubo Syndrome in a Neuromuscular Disorder |
title_full |
Noncompaction and Takotsubo Syndrome in a Neuromuscular Disorder |
title_fullStr |
Noncompaction and Takotsubo Syndrome in a Neuromuscular Disorder |
title_full_unstemmed |
Noncompaction and Takotsubo Syndrome in a Neuromuscular Disorder |
title_sort |
noncompaction and takotsubo syndrome in a neuromuscular disorder |
publisher |
Hindawi Limited |
series |
Case Reports in Cardiology |
issn |
2090-6404 2090-6412 |
publishDate |
2019-01-01 |
description |
Background. Takotsubo syndrome (TTS) in patients with left ventricular hypertrabeculation/noncompaction (LVHT) has been reported in four patients, and a TTS plus LVHT plus a neuromuscular disorder (NMD) was only reported once so far. Here, we present the fifth patient with LVHT and TTS and the second patient with LVHT, TTS, and a NMD. Methods and Results. The patient is a 68 yo female hobby choir singer with a history of skin dermatofibroma, skin fibrokeratoma, arterial hypertension, hyperlipidemia, hypothyroidism, anemia, hyponatremia, diverticulosis, LVHT detected at age 60 y, five syncopes, a liver cyst, and carotid endarterectomy 2 months prior to admission because of sudden-onset chest pain. Workup revealed ST elevation, troponin elevation, and mild coronary artery sclerosis. Ventriculography and transthoracic echocardiography (TTE) showed the apical type of a TTS. ECG normalised within 10 w and TTE within 6 w under beta-blockers and ATII-blockers. The TTS was triggered by being offended of being unable to sing anymore after endarterectomy. Neurological workup suggested the presence of a NMD. Conclusions. This case shows that LVHT occurs in NMD patients and that patients with LVHT and a NMD may develop a TTS. Whether patients with LVHT and a NMD are particularly prone to develop a TTS requires further confirmation. NMD patients with LVHT should avoid stress not to trigger a TTS. |
url |
http://dx.doi.org/10.1155/2019/6902751 |
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