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AA amyloidosis is a classic and serious complication of many chronic inflammatory processes, whether of infectious, autoimmune, or neoplastic origin. It is frequently complicated by kidney damage, often in the form of a nephrotic syndrome. Giant cell arteritis is a common inflammatory arteritis in the elderly; however, it rarely causes AA amyloidosis. We report a rare case of Horton disease causing AA amyloidosis in an elderly patient with history of myopericarditis and repeated episodes of congestive heart failure. Patient was treated initially with dual therapy based on corticosteroids and anti TNF therapy (Tocilizumab) associated with heart failure therapy recommended by the European society of cardiology (ESC 2021 guidelines on Heart Failure). The initial outcome was favorable but later complicated by the involvement of the lungs; pulmonary fibrosis, responsible for repeated episodes of pleural effusion non controlled in spite of high dose of loop diuretics and repeated pleural punction. Patient died shortly after her second hospitalization due to respiratory insufficiency.
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Hypertrophic cardiomyopathy (HCM) is the most common non-ischemic cardiomyopathy with a prevalence of 1:500 in the general population, based on the recognition of the phenotype. HCM is defined by the presence of increased left ventricular (LV) wall thickness that is not solely explained by abnormal loading conditions and the phenotype also includes disorganized myocyte arrangement, fibrosis, small-vessel disease, and abnormalities of the mitral valve apparatus. In particular to this pathology, we have conducted a one-year prospective study to determine clinical, echocardiographic features and etiopathogenic aspects of hypertrophic cardiomyopathy in the Casablanca university hospital. The results concluded that 50% of the causes was due to amyloidosis 35%, sarcomeric HCM and 15% Fabry disease in which 2 cases were related with pregnancy. Transthoracic echocardiography and cardia MRI plays an important role in HCM diagnosis and prognosis.
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Valsalva sinus aneurysm (SVAs) and double-chambered right ventricle (DCRV)is an uncommon congenitalheart defect and are usually associated with ventricular septal defect (VSD) in 50% to 60% of patient抯 population. The current case report had documented a 59 years old hypertensive asymptomatic male with a known case of SVAs presented to our hospital following device closure for 6 months. On examination, the patient was diagnosed to have DCRV induced by SVAs prior to the closure along with other factors. However, to the best of our knowledge, this is the first case report on DCRV induced by SVAs in synergy with other associated multifactors and without VSD among the Indian population.
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Introduction: The presence of a Q-wave on a 12-lead electrocardiogram (ECG) has been considered a marker of a large myocardial infarction (MI). However, the correlation between the presence of Q-waves and nonviable myocardium is still controversial. The aims of this study were to 1) test QWA, a novel ECG approach, to predict transmural extent and scar volume using a 3.0 Tesla scanner, and 2) assess the accuracy of QWA and transmural extent. Methods: Consecutive patients with a history of coronary artery disease who came for myocardial viability assessment by CMR were retrospectively enrolled. Q-wave measurements parameters including duration and maximal amplitude were performed from each surface lead. A 3.0 Tesla CMR was performed to assess LGE and viability. Results: Total of 248 patients were enrolled in the study (with presence (n ¼ 76) and absence of pathologic Q-wave (n ¼ 172)). Overall prevalence of pathologic Q-waves was 27.2% (for LAD infarction patients), 20.0 % (for LCX infarction patients), and 16.8% (for RCA infarction patients). Q-wave area demonstrated high performance for predicting the presence of a nonviable segment in LAD territory (AUC 0.85, 0.77e0.92) and a lower, but still significant performance in LCX (0.63, 0.51e0.74) and RCA territory (0.66, 0.55e0.77). Q-wave area greater than 6 ms mV demonstrated high performance in predicting the presence of myocardium scar larger than 10% (AUC 0.82, 0.76e0.89). Conclusion: Q-wave area, a novel Q-wave parameter, can predict non-viable myocardial territories and the presence of a significant myocardial scar extension.
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SARS Cov2 infection is a pandemic declared by WHO in early month of 2020 as corona virus disease (COVID 19) which was diagnosed first in Wuhan, China in December 2019. During first wave of COVID 19 we faced with severe acute respiratory insufficiency and respiratory failure with common symptoms of high-grade fever, shortness of breath and loss of sensations but later on we accessed the different symptoms to related with multi systems of human body. Cardiac emergencies or cardiovascular morbidities with mortality were accessed across the globe during COVID 19 pandemic era. Data revealed that SARS Cov2 affected on heart by both direct or indirect pathway which leads to acute myocarditis, myocardial injury/infarct, heart failure, thrombosis and arrhythmias. Here we are presenting a rare case as hematoma in myocardium called as intramyocardial dissecting hematoma. Non-invasive diagnostic tools to prevent mortality in cardiology field and avoid further complication.
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ABSTRACT: Bicuspid aortic valve (BAV) disease is generally associated with thoracic aortic dilatation (TAD). Related factors include; genetical, morphological (valvular phenotype) and most recently, hemodynamic profiles associated with flow pattern and wall shear stress. Cardiac magnetic resonance 4D Flow (4DF) can give an integral evaluation of these later flow variables. Remarkable, different spectrums of flow and vortex direction exist in BAV that are related to the site of TAD (proximal or distal). Therefore, we present a 57 years old patient with BAV (Sievers 0) with anteroposterior leaflets distribution in which 4DF depicted an anteriorly and righthand oriented jet that correlated with the zone of grater AD; also, vortex rotation was counterclockwise, corresponding to the most frequent vortex type in BAV. In conclusion, 4DF is a powerful and ground-breaking tool that enhances our knowledge of BAV related aortopathy.
Subject(s)
Magnetic Resonance Imaging, Cine/methods , Bicuspid Aortic Valve Disease , Aortic Aneurysm , Aortic Diseases/physiopathology , Image Interpretation, Computer-Assisted , Cardiovascular Diseases/diagnostic imaging , Imaging, Three-Dimensional , Cardiac-Gated Imaging Techniques/methodsABSTRACT
OBJECTIVE: To assess the accuracy and potential bias of computed tomography (CT) ventricular volumetry using semiautomatic three-dimensional (3D) threshold-based segmentation in repaired tetralogy of Fallot, and to compare them to those of two-dimensional (2D) magnetic resonance imaging (MRI). MATERIALS AND METHODS: This retrospective study evaluated 32 patients with repaired tetralogy of Fallot who had undergone both cardiac CT and MRI within 3 years. For ventricular volumetry, semiautomatic 3D threshold-based segmentation was used in CT, while a manual simplified contouring 2D method was used in MRI. The indexed ventricular volumes were compared between CT and MRI. The indexed ventricular stroke volumes were compared with the indexed arterial stroke volumes measured using phase-contrast MRI. The mean differences and degrees of agreement in the indexed ventricular and stroke volumes were evaluated using Bland-Altman analysis. RESULTS: The indexed end-systolic (ES) volumes showed no significant difference between CT and MRI (p > 0.05), while the indexed end-diastolic (ED) volumes were significantly larger on CT than on MRI (93.6 ± 17.5 mL/m² vs. 87.3 ± 15.5 mL/m² for the left ventricle [p < 0.001] and 177.2 ± 39.5 mL/m² vs. 161.7 ± 33.1 mL/m² for the right ventricle [p < 0.001], respectively). The mean differences between CT and MRI were smaller for the indexed ES volumes (2.0–2.5 mL/m²) than for the indexed ED volumes (6.3–15.5 mL/m²). CT overestimated the stroke volumes by 14–16%. With phase-contrast MRI as a reference, CT (7.2–14.3 mL/m²) showed greater mean differences in the indexed stroke volumes than did MRI (0.8–3.3 mL/m²; p < 0.005). CONCLUSION: Compared to 2D MRI, CT ventricular volumetry using semiautomatic 3D threshold-based segmentation provides comparable ES volumes, but overestimates the ED and stroke volumes in patients with repaired tetralogy of Fallot.
Subject(s)
Humans , Bias , Heart Defects, Congenital , Heart Ventricles , Magnetic Resonance Imaging , Methods , Retrospective Studies , Stroke Volume , Tetralogy of FallotABSTRACT
Objectives: To evaluate the changes of left atrial volume (LAV) and the maximum ostial cross-sectional area (CAS) of pulmonary vein (PV) in atrial fibrillation (AF) patients after circumferential pulmonary vein isolation radiofrequency catheter ablation (CPVA-RFCA) and to explore their relationship to AF recurrence by enhanced cardiac MRI evaluation. Methods: Our research included in 2 groups: Control group, n=20 healthy subjects and AF group, n=78 patients whom were classified into 2 subgroups as Paroxysmal AF subgroup, n=46 and Persistent AF subgroup, n=32; 66 patients received CPVA-RFCA and based on 6 months post-operative recurrence, they were divided into another set of 2 groups: AF recurrent subgroup, n=17 and Non-AF recurrent subgroup, n=49. Pre- and 6 months post-operative maximum ostial CSA of PV were measured by enhanced cardiac MRI, LAV were obtained by 3D reconstruction and the differences were compared between AF group and Control group, Paroxysmal AF subgroup and Persistent AF subgroup, AF recurrent subgroup and Non-AF recurrent subgroup; their relationships to AF recurrence were studied.Results: Compared with Control group, AF group had increased LAV and elevated ostial CSA of superior PV (SPV), both P<0.05. Compared with Paroxysmal AF subgroup, Persistent AF subgroup had increased LAV and elevated ostial CSA of SPV, both P<0.05. Compared with pre-operative condition, at 6 months after the operation, Non-AF recurrent subgroup showed reduced ostial CSAs in left SPV (LSPV), right SPV (RSPV), right inferior PV (RIPV) and decreased LAV, all P<0.05;while AF recurrent subgroup showed expanded RSPV and increased LAV,allP<0.05.Post-operative reductions of LAV and ostial CSA of SPV had close correlation; multivariate Logistic regression analysis indicated that LAV (HR=1.05, P<0.01)and ostial CSA of RSPV(HR=1.09,P=0.05)were related to AF recurrence after RFCA. Conclusions: CAPV-RFCA could reverse left atrial and PV remodeling in AF patients, LAV and ostial CSA of RSPV were related to post-operative AF recurrence.
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BACKGROUND: We investigated the difference in right ventricle (RV) volume and ejection fraction (EF) according to the pulmonary valve (PV) annular extension technique during Tetralogy of Fallot (TOF) total correction.METHODS: We divided patients who underwent the procedure from 1993 to 2003 into two groups according to PV extension technique (group I: PV annular extension, group II: no PV annular extension) during TOF total correction. We then analyzed the three segmental (RV inlet, trabecular and outlet) and whole RV volume and EF by cardiac magnetic resonance imaging (MRI).RESULTS: Fourteen patients were included in this study (group I: 10 patients, group II: four patients; male: nine patients, female: five patients). Cardiac MRI was conducted after a 16.1 years TOF total correction follow-up period. There was no statistical difference in RV segmental volume index or EF between groups (all p>0.05). Moreover, the total RV volume index and EF did not differ significantly between groups (all p>0.05).CONCLUSION: The RV volume and EF of the PV annular extension group did not differ from that of the PV annular extension group. Thus, PV annular preservation technique did not show the surgical advantage compared to PV annular extension technique in this study.
Subject(s)
Female , Humans , Male , Bays , Follow-Up Studies , Heart Ventricles , Magnetic Resonance Imaging , Pulmonary Valve , Tetralogy of FallotABSTRACT
Congenital heart disease(CHD) is one of the main causes of newborn death,which makes the prenatal diagnosis of CHD the hot spot of perinatology.Fetal echocardiography has high sensitivity in diagnosing fetal CHD in mid-gestational age of pregnancy,and is considered world-widely as the gold standard.Rapid advance has been achieved for the past decades in the technology of fetal cardiac magnetic resonance imaging (MRI).The advantages of fetal cardiac MRI including broad vision of interest and good reproducibility could make up for the deficiency of fetal echocardiography.However,some technical problems significantly limit the clinical application of it.Nowadays,fetal cardiac MRI has been utilized as a supplementary method in prenatal diagnosis of fetal CHD.This article reviews the application,advantages and limitations of fetal cardiac MRI in fetal CHD diagnosis.
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BACKGROUND: We investigated the difference in right ventricle (RV) volume and ejection fraction (EF) according to the pulmonary valve (PV) annular extension technique during Tetralogy of Fallot (TOF) total correction. METHODS: We divided patients who underwent the procedure from 1993 to 2003 into two groups according to PV extension technique (group I: PV annular extension, group II: no PV annular extension) during TOF total correction. We then analyzed the three segmental (RV inlet, trabecular and outlet) and whole RV volume and EF by cardiac magnetic resonance imaging (MRI). RESULTS: Fourteen patients were included in this study (group I: 10 patients, group II: four patients; male: nine patients, female: five patients). Cardiac MRI was conducted after a 16.1 years TOF total correction follow-up period. There was no statistical difference in RV segmental volume index or EF between groups (all p>0.05). Moreover, the total RV volume index and EF did not differ significantly between groups (all p>0.05). CONCLUSION: The RV volume and EF of the PV annular extension group did not differ from that of the PV annular extension group. Thus, PV annular preservation technique did not show the surgical advantage compared to PV annular extension technique in this study.
Subject(s)
Female , Humans , Male , Bays , Follow-Up Studies , Heart Ventricles , Magnetic Resonance Imaging , Pulmonary Valve , Tetralogy of FallotABSTRACT
PURPOSE: We proposed a multi-physiological signals based real-time intelligent triggering system(MITS) for Cardiac MRI. Induced noise of the system was analyzed. MATERIALS AND METHODS: MITS makes cardiac MR imaging sequence synchronize to the cardiac motion using ECG, respiratory signal and second order derivative of SPO2 signal. Abnormal peaks due to arrhythmia or subject's motion are rejected using the average R-R intervals and R-peak values. Induced eddy currents by gradients switching in cardiac MR imaging are analyzed. The induced eddy currents were removed by hardware and software filters. RESULTS: Cardiac MR images that synchronized to the cardiac and respiratory motion are acquired using MITS successfully without artifacts caused by induced eddy currents of gradient switching or subject's motion or arrhythmia. We showed that the second order derivative of the SPO2 signal can be used as a complement to the ECG signals. CONCLUSION: The proposed system performs cardiac and respiratory gating with multi-physiological signals in real time. During the cardiac gating, induced noise caused by eddy currents is removed. False triggers due to subject's motion or arrhythmia are rejected. The cardiac MR imaging with free breathing is obtained using MITS.
Subject(s)
Arrhythmias, Cardiac , Artifacts , Complement System Proteins , Electrocardiography , Magnetic Resonance Imaging , Noise , RespirationABSTRACT
Objective: Non-compaction cardiomyopathy (NCC) is a genetic disorder characterized by the presence of an extensive trabecular layer of myocardium with intertrabecular recesses in communication with the ventricular cavity. The objective of this study is to evaluate the clinical and morphological characteristics of patients with NCC with and without systolic dysfunction assessed by cardiac magnetic resonance (CMR) imaging, as well as to discuss the value and limitations of echocardiography and CMR imaging in its diagnosis. Twenty patients diagnosed with NCC were retrospectively included. Studies were performed on a 1.5 Tesla resonator. The end-diastolic volume (LVEDV) and end-systolic volumen (LVESV), end-diastolic diameter (LVEDD) and end-systolic diameter (LVESD), left ventricular ejection fraction (LVEF), cardiac mass and LV trabeculations were determined. A 17-segment myocardium segmentation model was applied. Student s T test was used to compare variables between groups. Significance level was set at p <0.05. Correlation between 2 continuous variables was calculated using the linear regression model. The statistical software package used for data analysis was StatsDirect (Version 2.6.5,. Altrincham, UK. Results: The average thickness of NC myocardial segments and normal myocardium was 13.1 +/- 3.3 mm and 3.6 +/- 0.6 mm, respectively. The average number of myocardial segments with NC was 8.2 +/- 1.2. The more affected segments were the apex of the heart and the lateral segments at the apical and mid-ventricular level. LVEDD, LVEDV, global LV mass, compacted and trabeculated, were significantly increased in the group of patients with ventricular dysfunction. LVEF had a negative linear correlation with trabecular myocardal mass (MM)/ m2 (R = 0.67, p = 0.001), LVEDV /m2 (R = 0.77, p <0.001) and LVEDD/m2 (R = 0.7, p <0.001). Similarly, a negative linear correlation between LVTM/m² and LVEDV/m² (R = 0.76, p < 0.001) was observed. Conclusion: In our population...
Objetivos: La miocardiopatía no compactada (MNC) es un desorden genético caracterizado por la presencia de una extensa capa de miocardio trabeculado con recesos intertrabeculares comunicados con la cavidad ventricular. El objetivo del trabajo es evaluar las características clínicas y morfológicas de los pacientes con MNC con y sin disfunción sistólica evaluados por resonancia magnética cardíaca (RMC), y poner en discusión los alcances y las limitaciones de la ecocardiografía y la RMC en su diagnóstico. Material y métodos: Se incluyeron en forma retrospectiva 20 pacientes con diagnóstico de MNC. Los estudios se realizaron en un resonador de 1.5 Tesla. Se determinaron: volumen de fin de diástole (VFDVI) y sístole, diámetro de fin de diástole (DFDVI) y sístole, fracción de eyección (FEVI), masa cardíaca y trabeculaciones del VI. La distribución del miocardio NC se llevó a cabo con el modelo de 17 segmentos miocárdicos. Se empleó el test de Student para comparar las variables entre ambos grupos. El nivel de significancia fue establecido en p < 0,05. La correlación entre 2 variables continuas se calculó usando el modelo de regresión lineal. Los análisis se realizaron utilizando el software de estadística StatsDirect (versión 2.6.5, Altrincham, UK). Resultados: El espesor medio del miocardio NC y el miocardio normal fue 13.1 +/- 3.3 mm y 3.6 +/- 0.6 mm respectivamente. El número medio de segmentos con miocardio NC fue 8.2 +/- 1.2, siendo los más afectados el ápex y los segmentos laterales a nivel apical y medioventricular. El DFDVI, el VFDVI, la masa global, compactada y trabeculada del VI estuvieron incrementados en forma significativa en el grupo de pacientes con disfunción ventricular. La FEVI tuvo una correlación lineal negativa con masa de miocardio trabeculado del VI (MTVI)/m2 (R = 0.67, p = 0.001), el VFDVI/m2 (R = 0.77, p < 0.001) y el DFDVI/m2 (R = 0.7, p < 0.001). Asimismo, hubo una correlación lineal negativa entre la MTVI/m2 y el VFDVI/m2...
Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Cardiomyopathies/pathology , Magnetic Resonance Imaging/methods , Cardiac Imaging Techniques/methods , Ventricular Dysfunction, Left , Echocardiography , Retrospective Studies , Ventricular Function, Left , Myocardium/pathology , Stroke VolumeABSTRACT
This study described the radiological features on echocardiography and MRI specific to cardiac amyloidosis confirmed on biopsy.Eleven cases of biopsy-proven cardiac amyloidosis were retrospectively reviewed in this study.All patients underwent biopsy,cardiac MRI and echocardiography.The main echocardiography and MRI findings were as follows: diffuse ventricular and septum wall thickening,atrial enlargement,pericardial effusion,restricted left ventricular(LV)systolic and diastolic function,characteristic granular sparkling of myocardium.MRI revealed a characteristic pattern of global subendocardial late enhancement,extending in varying degrees into the neighboring myocardium.The findings agreed with the infiltration distribution of amyloid protein.Typical abnormalities seen on echocardiography and MRI should have important diagnostic and prognostic value of cardiac amyloidosis.MRI should be considered in the diagnosis of cardiac amyloidosis if echocardiographic features are suspicious.
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Recently, MRI has achieved many technical advances in the spatial resolution, temporal resolution, signaltonoise ratio, and postprocessing software. As a result, cardiac MRI has made a sudden rise from old obscurity in the diagnosis of coronary artery disease. Cardiac MRI may be a onestopshop solution for the assessment of systolic dysfunction, perfusion impairment and myocardial viability, and for the imaging of stenosed artery. The evaluation of myocardial ischemia and viability are very important in the decision of therapeutic strategy and the anticipation of the prognosis of the patients with ischemic heart disease. At one session of examination, MRI can provide combined information on myocardial contractile function and myocardial perfusion, and unique information on the transmural extent of delayed hyper-enhancement. Delayed hyperenhancement on contrastenhanced MRI is highly reproducible irrespective of the scanning procedure and the operator, which is used for the interpretation of myocardial viability in the patients with myocardial infarction. Cardiac MRI is a very accurate and costeffective modality for the evaluation of ischemic heart disease.
Subject(s)
Humans , Arteries , Coronary Artery Disease , Diagnosis , Magnetic Resonance Imaging , Myocardial Infarction , Myocardial Ischemia , Perfusion , PrognosisABSTRACT
To examine the usefulness of cardiac MRI in assessing patients (pt) with congenital heart diseases(CHD), informations obtained from MRI and echocardiogrphy (echo) were compared in 91 consecutive pt with CHD and was correlated with findigs at cardiac catheterization (53pt) and at surgery (71pt). Pt were studied with 1.5 Tesla MRI unit and multiplanar images of the heart and great vessels were obtained using ECG-gated multislice spin-echo technique. Age ranged from newborn to 22 years. We obtained the following results. MRI was vary useful in providing important diagnostic informations in 19pt, provided informations which was not crucial to the clinical decision in 28pt, and did not provide additional informations in 44pt. MRI was very useful in assessing complex lesions, particularly in identifying atrial situs, rudimentary ventricular chamber, criss-cross atrioventricular connection, total anomalous pulmonary venous connection, anatomy of ventricular septal defect in double outlet right ventricle, anomalous ventricular muscles, aortopulmonary collateral artery and distal pulmonary artery anatomy. En face view of the ventricular septum was very useful in clearly outlining the ventricular septal defect. MRI gave false information in 17pt. Diagnostic accuracy of MRI was poor for coarctation of the aorta in neonates and small infants, patent ductus arteriosus and pulmonary stenosis. Cardiac MRI is recommended for preoperative planning in selected pt with CHD, particularly with complex lesions.