Cardiac Masses tumors By Dr Khaled M Abdel
Cardiac Masses tumors By Dr. Khaled M. Abdel Aal MD Cardiothoracic surgery Associate Prof. & Consultant of Cardiothoracic surgery Sohag University
Cardiac Masses Items to be covered: �Introduction �Classification �Presentation �Evaluation �Common types �Summary
Introduction � Improvement of cardiac Imaging and Surgery have changed cardiac tumors from a postmortem curiosity to a ready diagnosed and frequently treatable form of heart disease. �Cardiac tumors can be located in the Epicardium, Myocardium, and Endocardium. � Either primary or secondary. �Secondary tumors are commonest.
Introduction Prevalance: �Primary tumors �<3/10, 000 autopsies �Over ¾ are benign �Secondary � 20 -40 x more common �Present in upto 20% of patients dying of malignancy
Classification I. Primary cardiac tumors: �Benign �Malignant II. Secondery cardiac tumors: �Benign �malignant
Primary cardiac tumors �Benign: �Myxoma �Papillary fibroelastoma �Fibroma �Lipoma �Rhabdomyomas • Malignant: Angiosarcomas Rhabdomyosarcomas Mesotheliomas Lymphoma Intrapericardial Pheochromocytomas
Secondary Cardiac Tumors § Malignant: �Carcinoma (common) �Melanoma �carcinoid § Benign: �Intracardiac. Thrombus �Leiomyomatosis �Endomyocardial fibrosis
Presentation �Embolization � Systemic � Pulmonary (less common) �Obstruction �Arrhythmia �Tamponade �Direct compression of coronary artery �Intramyocardial � Conduction disturbances � Global dysfunction due to infiltration
Normal Variants on Echo �Many benign findings on echo often misinterpreted as pathologic: 1. Eustatian valve 2. Catheters 3. crista terminalis 4. Suture line 5. coronary sinus 6. moderator band 7. muscle bundles 8. False chords 9. Trabeculations 10. Brachiocephalic vein
Benign Primary Cardiac Tumors Myxomas �The most common primary cardiac tumor in the Age > 35 �Arise from the endocardium � 75% in the Lt. Atrium near fossa ovalis � 15% Rt. Atrium � 5 -10% Lt. Ventricle � 5% multiple sites
Myxomas �Grossly �Typically pedunculated �Gelatinous consistency �Friable �Histologically �Copious mucopolysaccharide stroma �Scattered solitary or clustered polygonal cells.
Myxoma � 90% are solitary, average size 5 -6 cm (range 1 -15 cm) �Average of presentation is 50 years old �Presentation: 1. Embolisation 2. Heart failure (obstruction, arrhythmia) 3. Constitutional manifestations
Myxoma Constitutional Extra cardiac manifestations suggestive of Collagen Vascular disease �Fever �ESR elevation �Anemia �Thrombocythemia �Circulating autoantibodies
Myxoma �Usually occur sporadically but at least 7 % occur as a part of an autosomal dominant syndrome called Carney Complex �spotty pigmentation of the skin �Peripheral myxoid tumors (cutaneous myxoma, myxoid mamary fibroadenoma) �Endocrine over activity (Cushing’s syndrome, pituitary adenomas, testicular Sertoli cell tumors)
Myxoma Management �High propensity for embolization �Surgical results excellent �Treatment is surgical with en bloc resection including rim of septum around base
Myxoma Management �Recurrence in about 1 -5% of cases (incomplete resection, implantation from first tumor etc) �therefore annual surveillance recommended �In the familial Carney complex – risk of recurrence 12 -22%
Papillary Fibroelastomas �Benign papilloma of endocardium �Average of detection is 60 years old �Found equally in men and women �Many are clinically silent but can result in emboli
Papillary Fibroelastoma – Echo Features � 90% are single, with median diameter of 8 mm �Most commonly found on downstream side of valves (can be confused for vegetations) �Less common locations: Papillary muscle, chordae tendenae or atria �Mobility is common and risk factor for embolization �Valvular regurgitation is rare
Papillary Fibroelastoma – Treatment �Most recommend resection, especially for left sided lesions �Risk of embolism can be up to 25% over 3 years and 6% in asymptomatic patients in whom the fibroelastoma was found incidentally �Surgery can usually be valve-sparing �Recurrences have not been reported
Cardiac Lipomas �Uncommon benign tumor, usually small and found on epicardial surface �True lipomas are rare, more often present as lipomatous hypertrophy of the interatrial septum �Highly echogenic �Usually present in inferior and superior portions of the septum with sparing of fossa ovalis “dumbell-shaped”
Cardiac Lipomas �Associated with atrial arrhythmias �No enhacement on MRI, decreased signal with fat suppression �True lipomas resection �Lipomatous hypertrophy surgery only if SVC obstructed or significant arrhythmias
Rhabdomyomas and Fibromas �Most common cardiac tumor in children �Rhabdomyomas occur within a cavity or embedded within myocardium, usual small and multiple; often regress on own �Fibromas are well-demarcated, echogenic masses that can extend into cavity and result in obstruction and arrhythmia; often found in free wall of LV �On MRI rhabomyomas are hyperintense on T 2, while fibromas are hypointense on T 2 and iso-intense after gadolinium
Malignant Primary Cardiac Tumors Angiosarcoma �Most common primary malignancy of the heart �Malignant cells that form vascular channels �Most commonly affect the � Rt. Heart � Rt. Atrium �Pericardium � Hemorrhagic � Thrombus effusion
Malignant Primary Cardiac Tumors …Angiosarcomas: �Diffuse, irregularly shaped �Mean survival one year �Successful Rx with Chemo and XRT followed by transplant reported
Malignant Primary Cardiac Tumors Rhabdomyosarcomas �Most commonly seen in adults �No chamber selectivity �No pericardial involvement �Multiple sites of cardiac involvement is common �Poor prognosis �Limited success with resection and adjuvant Rx.
Malignant Secondary Cardiac Tumors �Metastases can manifest in the heart as a mass, pericardial disease, myocardial involvement �Tumors can spread to heart by: direct invasion, spread through venous system or hematongenously �Cardiac involvement is often established at autopsy in patients with otherwise widely metastatic disease
Metastatic Disease to the Heart Primary Malignancy Cardiac Effect Lung Direct extension, effusion Breast Hematogenous/lymphatic spread, effusion Lymphoma Lymphatic spread, variable effects GI Variable Melanoma Intracardiac and myocardial Involvement Renal Cell Carcinoma IVC-RA-RV extension, can look like thrombus Carcinoid Tricuspid and pulmonic valve abnormalities
Intracardiac Thrombus �Intracardiac source of emboli account for approximately 15 -20% of strokes �TEE is imaging modality of choice for evaluation of intracardiac thrombus and source of emboli (except for LV apex) �Major sources: LA (45%), LV apex, aorta, valve prosthesis, abnormal interatrial septum (aneurysm)
Imaging Intracardiac Thrombus �Transthoracic Echo with/without contrast – best for LV thrombi associated with aneurysm or akinesis of the apex �TEE – best for all other locations of thrombus �MRI – excellent way to identify thrombus; usually identified on spin echo and gadolinium enhanced images with delayed enhancement
LV Thrombus – Echo Features �Sensitivity of TTE to detect LV thrombus is 7595% �Associated with myocardial infarction that results in akinesis of the apex or dilated cardiomyopathy resulting in slow flow �May be multiple, mobile �Texture usually distinct from myocardium �Risk factors for embolism: large size, mobility, and protrusion into LV cavity �TTE used to follow LV thrombi over time
LA Thrombus – Echo Features �LA appendage is most likely site �Associated conditions: Atrial Fibrillation, mitral stenosis, LV failure �The LAA can be multi-lobed in up to 70% of patients �Sensitivity of TEE to detect an LA thrombus approaches 95%, with equally high specificity �TEE evaluates size, mobility, emptying velocity, extension into LA, and interatrial aneurysm if present �Can also assess spontaneous echo contrast
Summary �Primary Cardiac tumors are rare and usually benign �Clinical presentation based on location and size of mass �Echo (TTE and TEE) remains the initial imaging test �CMR is a useful modality to further characterize intracardiac masses (especially lipomas, angiosarcomas and thrombi) and narrow the differential diagnosis �Treatment usually involves surgery for tumors
Thank you
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