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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Main Authors: Josef Finsterer, Claudia Stöllberger, Walter Benedikt Winkler
Format: Article
Language:English
Published: Hindawi Limited 2019-01-01
Series:Case Reports in Cardiology
Online Access:http://dx.doi.org/10.1155/2019/6902751
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spelling 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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