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CASE REPORT
Year : 2020  |  Volume : 30  |  Issue : 3  |  Page : 174-176

Apical hypertrophic cardiomyopathy masked by Takotsubo syndrome


1 Cardiac Imaging Department, Fondazione Cardiocentro Ticino, Lugano, Switzerland; Postgraduate School in Cardiovascular Diseases, University of Milan, Milan, Italy
2 Cardiac Imaging Department, Fondazione Cardiocentro Ticino, Lugano, Switzerland
3 Cardiac Imaging Department, Fondazione Cardiocentro Ticino, Lugano, Switzerland; Postgraduate School in Cardiovascular Diseases, University of Bari, Bari, Italy

Date of Submission01-May-2020
Date of Decision06-Jun-2020
Date of Acceptance10-Jul-2020
Date of Web Publication05-Nov-2020

Correspondence Address:
Elisa Gherbesi
Fondazione Cardiocentro Ticino, Via Tesserete 48, 6900 Lugano

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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jcecho.jcecho_46_20

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  Abstract 


We describe the case of a 66-year-old female presented to our emergency department (ER) with acute chest pain and diagnosed with Takotsubo syndrome that initially prevented from suspecting an apical hypertrophic cardiomyopathy at echocardiography.

Keywords: Apical hypertrophic cardiomyopathy, cardiac magnetic resonance imaging, echocardiography, Takotsubo cardiomyopathy


How to cite this article:
Gherbesi E, Paiocchi VL, Leo LA, Schlossbauer SA, Chiarello G, Faletra FF. Apical hypertrophic cardiomyopathy masked by Takotsubo syndrome. J Cardiovasc Echography 2020;30:174-6

How to cite this URL:
Gherbesi E, Paiocchi VL, Leo LA, Schlossbauer SA, Chiarello G, Faletra FF. Apical hypertrophic cardiomyopathy masked by Takotsubo syndrome. J Cardiovasc Echography [serial online] 2020 [cited 2020 Nov 24];30:174-6. Available from: https://www.jcecho.org/text.asp?2020/30/3/174/300089




  Introduction Top


Takotsubo syndrome (TTS) is characterized by transient left ventricular dysfunction and apical ballooning without obstructive coronary artery disease.[1] Hypertrophic cardiomyopathy (HCM) is a genetic disorder; apical HCM (ApHCM) is a variant characterized by hypertrophy of the ventricular apical myocardium.[2] We describe the case of a patient whose diagnostic suspicion of ApHCM was initially masked by her presentation with TTS.


  Case Report Top


A 66-year-old female presented to our ER with acute chest pain associated with cold sweat and dizziness. Her medical history was significant only for a minor stroke related to patent foramen ovale, for which she was treated with aspirin 100 mg/day.

On admission, blood pressure was 113/78 mmHg; oxygen saturation was 97% on room air. A 12-lead electrocardiogram (ECG) documented sinus rhythm 109 bpm with ST elevation in the inferolateral leads, so the patient underwent emergency invasive coronary angiography with a presumptive diagnosis of an acute ST elevation myocardial infarction. No significant coronary artery stenosis were detected and left ventriculography showed mid-apical akinesia, a pattern consistent with TTS [Figure 1]. No obvious stressful trigger was identified. At laboratory studies, troponin T was 503 ng/dL and creatine kinase-MB 53 U/L.
Figure 1: Left ventriculography with apical ballooning

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A transthoracic echocardiogram [Figure 2] confirmed mid-apical akinesia with hypercontractility of the basal segments without obstruction of the left ventricular outflow tract and a moderate reduction of the left ventricular systolic function (left ventricular ejection fraction [LVEF] 35%). Four days later, an echocardiogram [Video 1] documented apical akinesia with hypercontractility of the mid-basal segments, LVEF 50%, and increased wall thickness, which was attributed to edema (thickness of septum and posterior wall = 12 mm).
Figure 2: Echocardiogram during acute phase, apical 4-chamber view with apical ballooning

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Her hospital course was uneventful and the patient was discharged on bisoprolol, ramipril, and torasemide. Upon discharge, a repeat ECG showed negative T waves in the precordial (V3–V6) and inferior leads [Figure 3].
Figure 3: Electrocardiogram at discharge

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An echocardiogram scheduled at 1 month after discharge [[Figure 4] and Video 2] documented normal kinesis and LVEF 74%, compatible with recovery after TTS, but also thickened apical ventricular segments (thickness of lateral apex = 12 mm) and apical systolic cavity obliteration, confirmed with contrast echocardiography (Sonovue), suspected for ApHCM [Video 3].
Figure 4: Echocardiogram from apical view after recovery. (a) 4-chamber view; (b) 2-chamber view; (c) Three-dimensional 4-chamber view; (d) contrast echocardiogram 4-chamber view

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Cardiac magnetic resonance (CMR) was therefore scheduled.

3T CMR (Magnetom Skyra, Siemens) [Figure 5] confirmed the echocardiogram findings and T2 mapping excluded the presence of edema in the thickened myocardial segments (values <45 ms). T1 mapping documented an increase of myocardial T1 values of mid-apical segments, with an increase of extracellular volume (ECV) values (36%, normal value <25%), but no late gadolinium enhancement was observed. These data were suggestive of a diagnosis of ApHCM.
Figure 5: Cardiac magnetic resonance, 4-chamber, 2-chamber, and 3-chamber view. (a) (1–3): Cine steady-state free precession sequences; (b) (1–3): Late gadolinium enhancement; (c) (1–3): T2 mapping; (d) (1–3): T1 mapping

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A regular follow-up with echocardiography and 24-h ECG monitoring was, therefore, programmed.


  Discussion Top


Previous case reports in literature documented myocardial edema in the subacute phase of TTS,[3] responsible for thickening of the involved segments and mimicking ApHCM.[4],[5]

In the above-described case, the increased thickness of the apical ventricular segments after the acute phase of TTS was not related to edema, suggesting that ApHCM was not evident until fully recovery of the apical ballooning, making it a challenging diagnosis.

To our knowledge, this is the first reported case in which ApHCM was masked at presentation by TTS with apical ballooning on echocardiography. CMR excluded the presence of edema as the cause of apical ventricular thickening but documented an increase in ECV, compatible with ApHCM.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Pelliccia F, Kaski JC, Crea F, Camici PG. Pathophysiology of Takotsubo syndrome. Circulation 2017;135:2426-41.  Back to cited text no. 1
    
2.
Jan MF, Todaro MC, Oreto L, Tajik AJ. Apical hypertrophic cardiomyopathy: Present status. Int J Cardiol 2016;222:745-59.  Back to cited text no. 2
    
3.
Neil C, Nguyen TH, Kucia A, Crouch B, Sverdlov A, Chirkov Y, et al. Slowly resolving global myocardial inflammation/oedema in Tako-Tsubo cardiomyopathy: Evidence from T2-weighted cardiac MRI. Heart 2012;98:1278-84.  Back to cited text no. 3
    
4.
Izgi C, Ray S, Nyktari E, Alpendurada F, Lyon AR, Rathore S, et al. Myocardial edema in Takotsubo syndrome mimicking apical hypertrophic cardiomyopathy: An insight into diagnosis by cardiovascular magnetic resonance. Heart Lung 2015;44:481-5.  Back to cited text no. 4
    
5.
Hwang HJ, Lee HM, Yang IH, Kim DH, Byun JK, Sohn IS. Evolutionary change mimicking apical hypertrophic cardiomyopathy in a patient with takotsubo cardiomyopathy. Echocardiography 2014;31:E293-5.  Back to cited text no. 5
    


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]



 

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