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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Abnormalities of the papillary muscle &#40;PM&#41; are a rare disorder that has been described in patients with hypertrophic cardiomyopathy<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#8211;3</span></a> or cardiac amyloidosis causing significant left ventricular outflow tract &#40;LVOT&#41; obstruction&#46; These anomalies are often challenging to diagnose with 2D echocardiography&#44; and real-time 3D echocardiography &#40;RT3D&#41; facilitates the diagnosis by providing accurate imaging and delineation of the spatial relationship between the cardiac structures&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Case report</span><p id="par0010" class="elsevierStylePara elsevierViewall">A 43-year-old black African woman&#44; asymptomatic at presentation &#40;blood pressure 105&#47;71<span class="elsevierStyleHsp" style=""></span>mmHg&#44; heart rate 82<span class="elsevierStyleHsp" style=""></span>bp<span class="elsevierStyleHsp" style=""></span>m&#44; body surface area 1&#46;52<span class="elsevierStyleHsp" style=""></span>m<span class="elsevierStyleSup">2</span>&#41;&#44; diagnosed with sickle cell disease&#44; was investigated for pulmonary hypertension in our department&#46; Echocardiography was requested for the assessment of cardiac function and estimation of pulmonary artery pressures&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">Full 2D and 3D transthoracic echocardiography &#40;TTE&#41; was performed and 3D images were acquired and analyzed using Philips Qlab offline analysis software&#46; The echocardiogram revealed a dilated left ventricle &#40;LV&#41; with normal wall thickness and good global systolic function&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">In parasternal long-axis 2D view&#44; the anterolateral PM appeared in an unusual position&#44; and in short-axis view and apical 4 chambers view &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Figure 1</a>&#41; it was clearly inserted lower than normal&#46; A complete Doppler assessment revealed no high velocity or turbulent flow pattern and no significant LVOT or intracavitary gradient was identified&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">3D echocardiography clearly showed the lower insertion of the PM and the hypertrophied chordae &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Figure 2</a>&#41;&#46; A follow-up echocardiography study was recommended to assess left ventricular hypertrophy but the patient died a few months later due to a subarachnoid hemorrhage&#46; No post-mortem was performed&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Discussion</span><p id="par0030" class="elsevierStylePara elsevierViewall">Anomalous insertion of PMs not causing LVOT obstruction is a rare abnormality&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#8211;4</span></a> RT3D is being increasingly used in the clinical setting to accurately identify cardiac structures and anatomy&#46;<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5&#44;6</span></a> Its role is mainly in providing additional spatial information to 2D TTE in the identification of complex anatomic structures&#46; The normal variant of low insertion of the anterolateral PM without LVOT obstruction may be observed in healthy individuals but an association with sickle cell disease cannot be excluded&#59; further investigations are needed to confirm this association&#46; To our knowledge&#44; this is the first case in sickle cell disease of an anomalous insertion of PMs not causing LVOT obstruction reported in the literature&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Ethical disclosures</span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Confidentiality of data</span><p id="par0035" class="elsevierStylePara elsevierViewall">The authors declare that they have followed the protocols of their work center on the publication of patient data and that all the patients included in the study have received sufficient information and have given their informed consent in writing to participate in the study&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Right to privacy and informed consent</span><p id="par0040" class="elsevierStylePara elsevierViewall">The authors have obtained the informed consent of the patients and&#47;or subjects mentioned in the article&#46; The author for correspondence is in possession of this document&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Protection of human and animal subjects</span><p id="par0045" class="elsevierStylePara elsevierViewall">The authors declare that no experiments were performed on humans or animals for this investigation&#46;</p></span></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conflicts of interest</span><p id="par0050" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare&#46;</p></span></span>"
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Image in Cardiology
Anomalous insertion of the papillary muscle in a patient with sickle cell disease: A normal variant with no left ventricular outflow obstruction
Inserção anómala do músculo papilar num doente com drepanocitose: Uma variante do normal sem obstrução do tracto de saída do ventriculo esquerdo
Inês Zimbarra Cabritaa,
Corresponding author
ines.cabrita05@imperial.ac.uk

Corresponding author.
, Julia Grapsaa, David Dawsona, Fausto J. Pintob,c, J. Simon R. Gibbsa, Petros Nihoyannopoulosb
a National Heart and Lung Institute, Hammersmith Campus, Imperial College London, United Kingdom
b Instituto Cardiovascular, Lisboa, Portugal
c Hospital de Santa Maria, Centro Académico de Medicina de Lisboa, Serviço de Cardiologia I, CCUL, Lisboa, Portugal
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Abnormalities of the papillary muscle &#40;PM&#41; are a rare disorder that has been described in patients with hypertrophic cardiomyopathy<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#8211;3</span></a> or cardiac amyloidosis causing significant left ventricular outflow tract &#40;LVOT&#41; obstruction&#46; These anomalies are often challenging to diagnose with 2D echocardiography&#44; and real-time 3D echocardiography &#40;RT3D&#41; facilitates the diagnosis by providing accurate imaging and delineation of the spatial relationship between the cardiac structures&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Case report</span><p id="par0010" class="elsevierStylePara elsevierViewall">A 43-year-old black African woman&#44; asymptomatic at presentation &#40;blood pressure 105&#47;71<span class="elsevierStyleHsp" style=""></span>mmHg&#44; heart rate 82<span class="elsevierStyleHsp" style=""></span>bp<span class="elsevierStyleHsp" style=""></span>m&#44; body surface area 1&#46;52<span class="elsevierStyleHsp" style=""></span>m<span class="elsevierStyleSup">2</span>&#41;&#44; diagnosed with sickle cell disease&#44; was investigated for pulmonary hypertension in our department&#46; Echocardiography was requested for the assessment of cardiac function and estimation of pulmonary artery pressures&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">Full 2D and 3D transthoracic echocardiography &#40;TTE&#41; was performed and 3D images were acquired and analyzed using Philips Qlab offline analysis software&#46; The echocardiogram revealed a dilated left ventricle &#40;LV&#41; with normal wall thickness and good global systolic function&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">In parasternal long-axis 2D view&#44; the anterolateral PM appeared in an unusual position&#44; and in short-axis view and apical 4 chambers view &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Figure 1</a>&#41; it was clearly inserted lower than normal&#46; A complete Doppler assessment revealed no high velocity or turbulent flow pattern and no significant LVOT or intracavitary gradient was identified&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">3D echocardiography clearly showed the lower insertion of the PM and the hypertrophied chordae &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Figure 2</a>&#41;&#46; A follow-up echocardiography study was recommended to assess left ventricular hypertrophy but the patient died a few months later due to a subarachnoid hemorrhage&#46; No post-mortem was performed&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Discussion</span><p id="par0030" class="elsevierStylePara elsevierViewall">Anomalous insertion of PMs not causing LVOT obstruction is a rare abnormality&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#8211;4</span></a> RT3D is being increasingly used in the clinical setting to accurately identify cardiac structures and anatomy&#46;<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5&#44;6</span></a> Its role is mainly in providing additional spatial information to 2D TTE in the identification of complex anatomic structures&#46; The normal variant of low insertion of the anterolateral PM without LVOT obstruction may be observed in healthy individuals but an association with sickle cell disease cannot be excluded&#59; further investigations are needed to confirm this association&#46; To our knowledge&#44; this is the first case in sickle cell disease of an anomalous insertion of PMs not causing LVOT obstruction reported in the literature&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Ethical disclosures</span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Confidentiality of data</span><p id="par0035" class="elsevierStylePara elsevierViewall">The authors declare that they have followed the protocols of their work center on the publication of patient data and that all the patients included in the study have received sufficient information and have given their informed consent in writing to participate in the study&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Right to privacy and informed consent</span><p id="par0040" class="elsevierStylePara elsevierViewall">The authors have obtained the informed consent of the patients and&#47;or subjects mentioned in the article&#46; The author for correspondence is in possession of this document&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Protection of human and animal subjects</span><p id="par0045" class="elsevierStylePara elsevierViewall">The authors declare that no experiments were performed on humans or animals for this investigation&#46;</p></span></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conflicts of interest</span><p id="par0050" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare&#46;</p></span></span>"
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ISSN: 21742049
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