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Artykuły w czasopismach na temat „Cardiac tumours”

Autor: Grafiati

Data publikacji: 2 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

Nihoyannopoulos, P. "Cardiac tumours." Current Opinion in Cardiology 1, no. 2 (1986): 286–91. http://dx.doi.org/10.1097/00001573-198603000-00025.

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Goddard, Martin J. "Cardiac tumours." Diagnostic Histopathology 24, no. 11 (2018): 453–60. http://dx.doi.org/10.1016/j.mpdhp.2018.10.003.

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Sharma, J., S. Sherchan, S. Pradhan, et al. "Primary Cardiac Tumours: Our Experience." Nepalese Heart Journal 8, no. 1 (2013): 8–11. http://dx.doi.org/10.3126/njh.v8i1.8329.

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Introduction Primary cardiac tumours are rare with autopsy incidence of less than 0.1 percent. We present our experience on surgical treatment of such tumours. Methods Since 2001, fifteen patients underwent surgical intervention for primary cardiac tumour at our centre. Mean age was 46.5 ± 17.5 years (range 20 to 73 years). There were eight female patients. Thirteen patients had atrial myxoma and the remaining two had primary malignant tumours. Surgical excision of the tumour was done under cardiopulmonary bypass and cardioplegic cardiac arrest. Results Complete excision was possible in all be

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Tasheva, Iveta. "Hepatocellular Carcinoma with Right Atrial Metastasis." General medicine and Clinical Practice 7, no. 1 (2024): 01–05. http://dx.doi.org/10.31579/2639-4162/131.

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Cardiac tumours may be primary or secondary-metastatic (malignant). Secondary cardiac tumours are much more common than primary cardiac tumours. Their frequency on large anatomical studies varies between 3.4% and 13.9%. Though cardiac metastases may originate from any malignant tumor, melanomas have the greatest propensity for cardiac involvement, and also carcinomas of the thorax, including breast, lung, and esophageal [12,13]. The routes of metastasis include direct invasion, hematogenous, lymphatic, or transvenous, especially through the inferior vena cava [9,10]. Cardiac involvement should

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Omale, Malia. "Cardiac Metastases: Secondary Tumours of the Heart." International Journal of Sciences Volume 6, no. 2017-01 (2017): 73–77. https://doi.org/10.5281/zenodo.3349339.

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Cardiac metastases are secondary tumours of the heart that originate from primary malignancy in other parts of the body. Secondary tumours are mostly diagnosed during post-mortem examination. However, the incidence rate of secondary cardiac tumours is much greater that of primary cardiac tumours. Secondary tumours are often diagnosed using imaging techniques such as TEE, TTE, CT scans and MRI. In most cases, a combination of these imaging methods is necessary to accurately diagnose the presence of a secondary cardiac tumour. In addition, surgical excision is the primary treatment option of sec

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Monther, Obeidat MD.* Yazan Qawasmeh MD. Hani Tarawneh MD. Alaa' Tawalbeh MD. Nuseibah Alramadina MD. "SURGICAL INTERVENTION IN PEDIATRIC HEART TUMORS." Indian Journal of Medical Research and Pharmaceutical Sciences 4, no. 4 (2017): 15–17. https://doi.org/10.5281/zenodo.546872.

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<strong>Background:</strong> cardiac tumours are rare in children. most cardiac tumours in children are benign and don’t need surgical intervention. Indications for surgical intervention include compression on the valves or vessels, heart failure and arrhythmias. <strong>Aim: </strong>to evaluate the types and presentation of cardiac tumours that required surgical intervention <strong>Methods:</strong> a retrospective study of all cardiac tumours in children needing surgical intervention at Queen Alia Heart Institute in Jordan between January 2015 and January 2017. Age at surgery, sex, present

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Dimassi, Adel, Wael Dimassi, and M. Samir Arnaout. "Giant right ventricular fibroma co-existing atrial septal defect in a 15 year old girl." Cardiology in the Young 19, no. 6 (2009): 630–32. http://dx.doi.org/10.1017/s1047951109990709.

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AbstractThe most common benign cardiac tumours are the myxomas, the rhabdomyomas, and the fibromas, with the latter 2 variants being the most common tumours encountered in children. The size and location of tumours within the heart create a variety of clinical findings, such as murmurs, chest pain, tachyarrythmias, and congestive cardiac failure. Nowadays, the tumours are usually diagnosed by echocardiography, magnetic resonance imaging and cardiac catheterization. Surgical excision is the treatment of choice if the tumour causes either arrhythmia or cavitary obstruction. In this report, we de

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Steger, Christina Maria, Thomas Hager, and Elfriede Ruttmann. "Primary Cardiac Tumours: A Single-Center 41-Year Experience." ISRN Cardiology 2012 (June 27, 2012): 1–7. http://dx.doi.org/10.5402/2012/906109.

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Primary cardiac tumours are extremely rare with the most commonest being left atrial myxomas. In general, surgical resection is indicated, whenever the tumour formation is mobile and embolization can be suspected. Within 17280 patients receiving heart surgery at the Innsbruck Medical University, 78 patients (0.45%) underwent tumourectomy of primary cardiac tumours. The majority of patients (63) suffered from a left or right atrial myxoma, 12 showed a papillary fibroelastoma of the valves at echocardiographical or histological examination, 1 suffered from a hemangioma, 1 from a chemodectoma, an

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9

Tavora, Fabio, and Allen Burke. "Pathology of cardiac tumours and tumour-like conditions." Diagnostic Histopathology 16, no. 1 (2010): 1–9. http://dx.doi.org/10.1016/j.mpdhp.2009.10.002.

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Shareq, Ahmed. "Left Ventricular Myxoma causing Dyspnoea in Paediatric Patient: A Rare Case Report." International Journal Of Medical Case Reports 4, no. 4 (2023): 5–8. https://doi.org/10.5281/zenodo.8416502.

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Cardiac tumours are a relatively rare entity in clinical practice, with an estimated prevalence of 0.0017-0.19% among the general population. Among these, myxomas represent the most common primary cardiac tumours, accounting for approximately 50% of cases. In paediatric age group these tumours are rare and when present they may present a diagnostic challenge because of the non-specific symptoms they produce. A high index of suspicion is necessary for the diagnosis of cardiac myxomas in paediatric age group. Any patient presenting with unexplained dyspnoea and signs of failure must be thoroughl

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11

Burnside, N., and S. W. MacGowan. "Malignant primary cardiac tumours." Interactive CardioVascular and Thoracic Surgery 15, no. 6 (2012): 1004–6. http://dx.doi.org/10.1093/icvts/ivs350.

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Hudzik, B., and L. Polonski. "Neglected conditions: Cardiac tumours." Canadian Medical Association Journal 186, no. 6 (2014): 452–53. http://dx.doi.org/10.1503/cmaj.114-0024.

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Basso, C. "Primary cardiac valve tumours." Heart 89, no. 10 (2003): 1259–60. http://dx.doi.org/10.1136/heart.89.10.1259.

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Burke, A., J. Jeudy, and R. Virmani. "Cardiac tumours: an update." Heart 94, no. 1 (2008): 117–23. http://dx.doi.org/10.1136/hrt.2005.078576.

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Basso, Cristina, Stefania Rizzo, Marialuisa Valente, and Gaetano Thiene. "Cardiac masses and tumours." Heart 102, no. 15 (2016): 1230–45. http://dx.doi.org/10.1136/heartjnl-2014-306364.

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Yadava, O. P. "Cardiac tumours in infancy." Indian Heart Journal 64, no. 5 (2012): 492–96. http://dx.doi.org/10.1016/j.ihj.2012.05.004.

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Qi, Xian-Jie, Ting Wei, Isah Amir Abba, et al. "The role of single-cell RNA sequencing in cardiac tumour - a case report." Journal of the Pakistan Medical Association 73, no. 12 (2023): 2462–64. http://dx.doi.org/10.47391/jpma.7776.

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A 65-year-old woman presented to our hospital with 5 days of chest tightness, dyspnoea, and lower abdominal distension. Echocardiography revealed a mass in the right atrium. An emergency operation was carried out to prevent tumour shedding. The patient was discharged on the 4th day of tumour resection, without any complications At the 18 months follow-up, she suffered from kidney and lung tumours. She refused any treatment and passed away. scRNA-seq was applied to analyse the nature of the tumour. The cellular components of benign tumours include chondrocytes, smooth muscle cells, fibroblasts,

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18

Darbari, Anshuman, Devender Singh, Shegu Gilbert, Barun Kumar, and Neha Singh. "Capillary haemangioma of the heart presenting with pericardial effusion: A case report." Journal of Cardiovascular and Thoracic Research 13, no. 3 (2020): 250–53. http://dx.doi.org/10.34172/jcvtr.2020.60.

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Cardiac haemangiomas (CH) are rare benign primary tumours of the heart and constitute nearly 2.8% of primary cardiac tumours. In a-48-year-old female, a cardiac tumour mass over right ventricular out flow area and main pulmonary artery was detected during diagnostic workup for aetiology of recurrent pericardial effusion. Echocardiograhy and pericardial fluid findings were non conclusive. Contrast enhanced Computed tomography (CECT) and Positron emission tomography (PET) scan imaging found the exophytic, moderately hypermetabolic, heterogeneous mass lesion posterolateral to main pulmonary trunk

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19

Kairemo, Kalevi, and Vivek Subbiah. "Molecular imaging of metastatic atrial angiosarcoma with positron emission tomography (PET) tracer 3′-deoxy-3′[(18)F]-fluorothymidine, [(18)F]-FLT imaging and early response evaluation." BMJ Case Reports 12, no. 5 (2019): e218979. http://dx.doi.org/10.1136/bcr-2016-218979.

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Primary cardiac angiosarcoma, the most common primary cardiac sarcoma has an incidence ranging from 0.001% to 0.028% in autopsy reports with around 200 cases reported in literature. Since a diagnosis of cardiac angiosarcoma portends a poor prognosis, it is vital to ascertain the precise extent of the lesions for follow-up. Imaging with positron emission tomography (PET) tracer 2-deoxy-2-[18F]-fluoro-D-glucose in cardiac angiosarcoma is challenging as myocardium takes up glucose and delineation of tumour becomes difficult. Cell proliferation rate in normal cardiac muscular tissue is low whereas

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Maroun, J., W. Kocha, L. Kvols, et al. "Guidelines for the Diagnosis and Management of Carcinoid Tumours. Part 1: The Gastrointestinal Tract. A Statement from a Canadian National Carcinoid Expert Group." Current Oncology 13, no. 2 (2006): 67–76. http://dx.doi.org/10.3390/curroncol13020006.

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Carcinoid tumours are relatively rare and, in general, slow growing. They can be “non-functioning” tumours, presenting as a tumour mass, or “functioning” tumours secondary to the production of several biopeptides leading to the carcinoid syndrome. Though these tumours represent 0.25% of an oncology practice, a proper understanding of the clinical course of the disease and of the importance of appropriate diagnostic and therapeutic measures is very important. Proper patient management can lead to cure, particularly if the tumour can be fully resected, or to long-term palliation with medical tre

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International, Journal of Medical Science and Innovative Research (IJMSIR). "Cardiac Myxoma- A Medical Enigma." International Journal of Medical Science and Innovative Research (IJMSIR) 9, no. 6 (2024): 121–24. https://doi.org/10.5281/zenodo.15449584.

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<strong>Abstract</strong> Cardiac myxomas are rare primary cardiac tumours presenting with diverse range of symptoms. Generally, the patients recover well if these tumours are diagnosed early and timely surgical intervention is provided. We present a case of an 85-year-old female who presented with complaints of chest pain and palpitations since 2 months. A Transthoracic Echocardiogram revealed a large mass attached to the interatrial septum protruding into the left ventricle. The possibility of intracardiac thrombus was given. The mass was excised and sent for histopathology which confirmed i

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22

Padalino, Massimo A., Elena Reffo, Alessia Cerutti, et al. "Medical and surgical management of primary cardiac tumours in infants and children." Cardiology in the Young 24, no. 2 (2013): 268–74. http://dx.doi.org/10.1017/s104795111300022x.

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AbstractPrimary cardiac tumours in infants and children are extremely rare, with an estimated incidence of 0.2% according to echocardiographic studies. Owing to their rarity, there is very little literature available, and most knowledge is based on collections of case reports. Therefore, we reviewed retrospectively our 27 years of clinical experience on the overall management of cardiac tumours among children in order to improve not only our knowledge but also to provide others with information about the incidence, clinical presentation, management, and long-term outcome of this rare disease.

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Chu, P.-H., S.-M. Jung, H.-H. Wu, et al. "Apoptosis in primary cardiac tumours." International Journal of Clinical Practice 58, no. 6 (2004): 564–67. http://dx.doi.org/10.1111/j.1368-5031.2004.00118.x.

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Komar, Monika. "Cardiac Tumours and Malignancy Diseases." Journal of Rare Cardiovascular Diseases 3, no. 6 (2018): 191. http://dx.doi.org/10.20418/jrcd.vol3no6.323.

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Bruce, C. J. "Cardiac tumours: diagnosis and management." Heart 97, no. 2 (2010): 151–60. http://dx.doi.org/10.1136/hrt.2009.186320.

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Butany, Jagdish, Vidhya Nair, Ather Naseemuddin, Girish M. Nair, Charles Catton, and Teri Yau. "Cardiac tumours: diagnosis and management." Lancet Oncology 6, no. 4 (2005): 219–28. http://dx.doi.org/10.1016/s1470-2045(05)70093-0.

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Myers, Kimberley A., Kenny K. Wong, Marion Tipple, and Shubhayan Sanatani. "Benign cardiac tumours, malignant arrhythmias." Canadian Journal of Cardiology 26, no. 2 (2010): e58-e61. http://dx.doi.org/10.1016/s0828-282x(10)70009-x.

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Groves, A. M., N. L. Fagg, A. C. Cook, and L. D. Allan. "Cardiac tumours in intrauterine life." Archives of Disease in Childhood 67, no. 10 Spec No (1992): 1189–92. http://dx.doi.org/10.1136/adc.67.10_spec_no.1189.

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Saiag, Esther, Michael Berant, Sara Kivity, and Leonard Blieden. "Cardiac tumours in tuberous sclerosis." European Journal of Pediatrics 154, no. 7 (1995): 589. http://dx.doi.org/10.1007/bf02074845.

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Takajo, Daiji, and Sanjeev Aggarwal. "A rhabdomyoma in the right ventricle presenting as hemodynamics of hypoplastic right heart." Cardiology in the Young 30, no. 10 (2020): 1527–29. http://dx.doi.org/10.1017/s1047951120002358.

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AbstractRhabdomyomas are the most common paediatric cardiac tumours. The natural history of these tumours is mostly benign, and the tumour usually regresses spontaneously. Although surgical resection of these tumours is one of the considerations in patients with ventricular outflow obstruction, a palliation with Blalock–Taussig shunt is an alternative approach with the hope of regression of the tumour over time. We report a case of prenatally diagnosed rhabdomyomas in the right ventricle and its outflow presenting as hemodynamic simulating hypoplastic right ventricle in a newborn. She required

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di Summa, Michele, and Federica Iezzi. "Giant Fibroelastoma of the Aortic Valve." Case Reports in Cardiology 2013 (2013): 1–2. http://dx.doi.org/10.1155/2013/754235.

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Fibroelastomas account for less than 10% of all cardiac tumours, representing the most common valvular and the second most common cardiac benign tumour, following myxomas. Fibroelastomas are histologically benign; they can result in life-threatening complications such as stroke, acute valvular dysfunction, embolism, ventricular fibrillation, and sudden death. Surgical resection should be offered to all patients who have symptoms and to asymptomatic patients who have pedunculated lesions or tumors larger than 1 cm in diameter. Valve-sparing excision produces good long-term results in most insta

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Facin, Mirella, Carlos Alberto Pastore, Nelson Samesima, and Horacio Gomes Pereira Filho. "Ventricular repolarization abnormalities: the electrocardiographic track of cardiac tumoural involvement in an infant with tuberous sclerosis complex. A case report." European Heart Journal - Case Reports 4, no. 2 (2020): 1–6. http://dx.doi.org/10.1093/ehjcr/ytaa025.

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Abstract Background Primary cardiac tumours are rare in children. Against this backdrop, Doppler echocardiogram is the main diagnostic procedure, while electrocardiogram (ECG) usually plays a secondary role, by detecting tumoural consequences as cardiac arrhythmias and chambers overload. We describe a case where an electrocardiographic sign was the cornerstone to diagnosis and surveillance of an infant with a cardiac rhabdomyoma. Case summary A female infant was referred for cardiac evaluation to elucidate an electrocardiographic abnormality, detected during investigation of seizures. She had

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Sundari, Abinaya, and Umamaheshwari Gurusamy. "Cardiac fibroma presenting as hypoplastic left heart syndrome in a foetus: causal or coincidental?" BMJ Case Reports 17, no. 3 (2024): e258742. http://dx.doi.org/10.1136/bcr-2023-258742.

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Primary cardiac tumours are very rare. Cardiac tumours in the perinatal period are even more uncommon with a prevalence of 0.0017% to 0.28% in autopsy series. The majority of benign cardiac tumours are cardiac rhabdomyomas, followed by cardiac fibromas. Another rare congenital heart disease is hypoplastic left heart syndrome (HLHS). Here we present a 21-week-old foetus diagnosed antenatally with HLHS on foetal echocardiogram. An autopsy done on the foetus following medical termination of pregnancy revealed a cardiac fibroma in the ventricular septum. It is very uncommon to have a combination o

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Faim, Diogo, Andreia Francisco, and António Pires. "Cardiac tumours in children: a single-centre experience and literature review." Cardiology in the Young 32, no. 3 (2022): 347–56. http://dx.doi.org/10.1017/s1047951122000531.

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AbstractCardiac tumours are extremely rare in children. Although more than 90% are benign, children can develop obstructive or embolisation derived symptoms, arrhythmias, constitutional symptoms, cardiac tamponade, or even sudden death. Although the majority are asymptomatic, and some spontaneously regress, appropriate follow-up is needed on a case-by-case basis, as patients may develop late symptoms. Definitive diagnosis is only possible through histological analysis; however, it is possible to infer tumour type with a high grade of certainty based on imaging features, particularly cardiac ma

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Sharma, Jayendra, Yasutaka Hirata, and Ralph S. Mosca. "Surgical repair in neonatal life of cardiac haemangiomas diagnosed prenatally." Cardiology in the Young 19, no. 4 (2009): 403–6. http://dx.doi.org/10.1017/s1047951109004168.

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AbstractAlthough cardiac tumours are rare, such tumours are increasingly being diagnosed with increasing frequency and great accuracy by antenatal ultrasound. Cardiac haemangiomas account for less than one-twentieth of all primary cardiac tumours, with most being diagnosed in the neonatal period. We report 3 instances of successful neonatal resection of cardiac haemangioma subsequent to prenatal diagnosis. Such diagnosis is important in perinatal management, since early surgical intervention provides a good prognosis.

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Bejiqi, Ramush, Ragip Retkoceri, and Hana Bejiqi. "Prenatally Diagnosis and Outcome of Fetuses with Cardiac Rhabdomyoma - Single Centre Experience." Open Access Macedonian Journal of Medical Sciences 5, no. 2 (2017): 193–96. http://dx.doi.org/10.3889/oamjms.2017.040.

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BACKGROUND: Cardiac rhabdomyoma (CRs) are the most common primary tumour of the heart in infants and children. Usually are multiple and, basing on the location can cause a haemodynamic disturbance, dysrhythmias or heart failure during the fetal and early postnatal period. CRs have a natural history of spontaneous regression and are closely associated with tuberous sclerosis complex (TSC). It has an association with tuberous sclerosis (TS), and in those, the tumour may regress and disappear completely, or remain consistent in size. AIM: We aimed to evaluate the prenatal diagnosis, clinica

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Shaikh, Moosa Ahmed, Dalia Ahmed, Neelaveni Duhli, and Claudette Phillips. "Right ventricle myxoma: an uncommon occurrence." BMJ Case Reports 17, no. 10 (2024): e260681. http://dx.doi.org/10.1136/bcr-2024-260681.

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Cardiac tumours are often an incidental finding; when they do cause symptoms, they can be systemic (pyrexia and fatigue), cardiac (arrhythmia, chest pain and obstructive) or embolic (stroke, pulmonary embolism (PE) and peripheral embolism). Different cardiac tumours have a higher prevalence in children when compared with adults, and each type of tumour has a predisposition for specific aspects of the heart. With current imaging modalities, it is possible to identify the location, haemodynamic impact and tissue characteristics of tumours, which can help diagnose the type of lesion and guide fur

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Salanitri, J., D. Lisle, C. Rigsby, R. Slaughter, and R. Edelman. "Benign cardiac tumours: Cardiac CT and MRI imaging appearances." Journal of Medical Imaging and Radiation Oncology 52, no. 6 (2008): 550–58. http://dx.doi.org/10.1111/j.1440-1673.2008.02010.x.

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Flores, Catalina, Jaclyn Lundberg, Randy R. Richardson, and Deepa Prasad. "Utility of cardiac imaging in diagnosis of atypical presentation of cardiac fibroma." BMJ Case Reports 12, no. 9 (2019): e230333. http://dx.doi.org/10.1136/bcr-2019-230333.

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Primary cardiac tumours are relatively rare in the paediatric population, with benign tumours accounting for >90% of cases. Cardiac fibromas are rare primary tumours that typically reside in the ventricles. Symptoms are usually the result of blood outflow obstruction or disruption of the cardiac conduction system. They do not typically regress and usually require surgical intervention. In this case, we report a rare finding of a right atrial fibroma in an 18-month-old female who presented with lethargy and vomiting. Chest X-ray revealed an enlarged cardiac silhouette, and follow-up CT showe

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Naseerullah, Fahad Syed, Hemangkumar Javaiya, and Avinash Murthy. "Cardiac Lipoma: An Uncharacteristically Large Intra-Atrial Mass Causing Symptoms." Case Reports in Cardiology 2018 (2018): 1–3. http://dx.doi.org/10.1155/2018/3531982.

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Primary tumours of the heart are often encountered in clinical practice. Different autopsy series estimate the incidence to be anywhere from 0.001% to 0.19%. Cardiac lipoma is a rare type of tumour of the heart and pericardium. It comprises approximately 10–19% of all cardiac tumours. We present a case of a large cardiac lipoma in a fifty-year-old female. She presented with sharp chest pains, palpitations, and dizziness. Acute coronary syndrome was ruled out. A transthoracic echocardiogram showed an abnormal, large, fixed right atrial mass. The mass was noted to be occupying most of the right

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Doksöz, Önder, Timur Mese, and Ayşegül Gulden Diniz. "Massive pericardial effusion caused by “Inflammatory Myofibroblastic Tumour” in a 3-month-old child." Cardiology in the Young 23, no. 5 (2012): 749–51. http://dx.doi.org/10.1017/s1047951112001849.

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AbstractTumours originating from cardiac tissues are rarely encountered during childhood, and fortunately most of these tumours are benign in nature. Inflammatory myofibroblastic tumour, which has unique clinical, pathological, and molecular characteristics, is a relatively new entity compared with previously mentioned tumoural processes originating from the heart. Most of the cardiac intima-media thickness patients are in the age group of 4 months to 17 years. This rarely seen tumoural process has not been subject of any specific research and the prognosis is not well known. Here we present t

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Sabzi, Feridoun, Aghigh Heydari, Mohammad Rouzbahani, Reza Heidari Moghaddam, and Atefeh Asadmobini. "Combination of cardiac and carotid glomus tumour: a rare case report." Folia Medica 64, no. 6 (2022): 1012–15. http://dx.doi.org/10.3897/folmed.64.e67448.

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The most common tumour of the heart is myxoma but paraganglioma (also called glomus tumour in extracardiac sites) in the cardiac position is the rarest of them. While this tumour accounts for 0.8% of all primary benign tumours, the combination of both neoplasms is an exceedingly rare occurrence. Herein, we present a case of combined carotid glomus tumour and left atrial paraganglioma tumour in which respiratory distress was the presenting symptom of cardiac type but carotid tumour was asymptomatic. The case underwent a two-step resection of the neck and cardiac mass with an uncomplicated posto

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Garcia-Carretero, Rafael, Gema Naranjo-Mansilla, Esther Luna-Heredia, Paloma Arias-Baldo, and Blanca-Nieves Beamonte-Vela. "Incidental Finding of a Left Atrial Myxoma while Characterising an Autoimmune Disease." Journal of Critical Care Medicine 4, no. 2 (2018): 64–67. http://dx.doi.org/10.2478/jccm-2018-0009.

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Abstract Although cardiac tumours are uncommon, cardiac myxomas account for more than fifty percent of all cases and are the most frequent primary cardiac tumour. They have a broad clinical spectrum, usually related to cardiac symptoms, peripheral embolic events or systemic manifestations. We present a case report of a 68-year-old man who presented with systemic symptoms and analytical features suggestive of an autoimmune disease. In the ensuing diagnostic procedures, a cardiac myxoma was found, and after surgical resection, both the systemic manifestations and the analytical abnormalities dis

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Shearer, B., R. A. Elderkin, C. Whight, and D. J. Radford. "Echocardiographic assessment of paediatric cardiac tumours." Heart, Lung and Circulation 9, no. 3 (2000): A86. http://dx.doi.org/10.1046/j.1443-9506.2000.05845.x.

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Fitzpatrick, A. P., J. G. Lanham, and D. V. Doyle. "Cardiac tumours simulating collagen vascular disease." Heart 55, no. 6 (1986): 592–95. http://dx.doi.org/10.1136/hrt.55.6.592.

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Hohneck, Anna Lena, Stephanie Rosenkaimer, Ralf-Dieter Hofheinz, Ibrahim Akin, Martin Borggrefe, and Stefan Gerhards. "Blood Cholesterol and Outcome of Patients with Cancer under Regular Cardiological Surveillance." Current Oncology 28, no. 1 (2021): 863–72. http://dx.doi.org/10.3390/curroncol28010085.

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Cardiovascular (CV) diseases and cancer share several similarities, including common risk factors. In the present investigation we assessed the relationship between cholesterol levels and mortality in a cardiooncological collective. In total, 551 patients receiving anticancer treatment were followed over a median of 41 (95% CI 40, 43) months and underwent regular cardiological surveillance. A total of 140 patients (25.4%) died during this period. Concomitant cardiac diseases were more common in patients who deceased (53 (37.9%) vs. 67 (16.3%), p < 0.0001), as well as prior stroke. There wer

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Grech, R., A. Mizzi, and S. Grech. "Compression of the Superior Vena Cava by an Interatrial Septal Lipoma: A Case Report." Case Reports in Pulmonology 2013 (2013): 1–3. http://dx.doi.org/10.1155/2013/945726.

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Primary cardiac tumours are rare; their prevalence ranges from 0.0017% to 0.28% in various autopsy series. Cardiac lipomas are well-encapsulated benign tumours typically composed of mature fat cells, and their reported size ranges from 1 to 15 cm. They are usually seen in the left ventricle and the right atrium. Lipomas are true neoplasms, as opposed to lipomatous hypertrophy of the interatrial septum, which is a nonencapsulated hyperplastic accumulation of mature and foetal adipose tissue. Cardiac lipomas occur in patients of all ages, and the frequency of occurrence has been found to be equa

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Shiono, Junko, Hitoshi Horigome, Seiyo Yasui, et al. "Electrocardiographic changes in patients with cardiac rhabdomyomas associated with tuberous sclerosis." Cardiology in the Young 13, no. 3 (2003): 258–63. http://dx.doi.org/10.1017/s1047951103000507.

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Background:Cardiac rhabdomyomas associated with tuberous sclerosis induce various abnormalities in the electrocardiogram. Electrocardiographic evidence of ventricular hypertrophy may appear if the tumour is electrically active. To our knowledge, electrocardiographic evidence of ventricular hypertrophy has been reported only in association with congestive heart failure. Follow-up studies of changes in electrocardiographic findings are also lacking.Methods:We studied 21 consecutive patients with cardiac rhabdomyoma associated with tuberous sclerosis, 10 males and 11 females, aged from the date o

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Tanindi, Asli, Gulten Tacoy, Fatma Hizal, et al. "Left ventricular myxoma: Confusing intracardiac mass in a patient with leukemia in remission." Open Medicine 5, no. 4 (2010): 437–41. http://dx.doi.org/10.2478/s11536-009-0105-7.

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AbstractCardiac myxomas are the most common primary benign tumors of the heart and appears particularly in the left atrium. Myxomas exhibit a wide spectrum of symptoms from asymptomatic to very serious according to the localisation of the tumours. Only 5% of these tumours occur in the right and left ventricles. We report an unusual case of a 21-year-old woman with a leukemia in remission, in whom routine transthorasic echocardiographic examination demonstrated an incidental left ventricular mass. The patient underwent successful resection of the left ventricular mass under cardiopulmonary bypa

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Janus, Izabela, Marcin Nowak, Agnieszka Noszczyk-Nowak, et al. "Epidemiological and pathological features of primary cardiac tumours in dogs from Poland in 1970–2014." Acta Veterinaria Hungarica 64, no. 1 (2016): 90–102. http://dx.doi.org/10.1556/004.2016.010.

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Primary heart tumours affect less than 1% of dogs. Due to their rare incidence, every research showing the frequency of cardiac tumours is valuable. Routine diagnostics is often complemented with immunohistochemical analysis. This study was conducted on 110 patient records from all veterinary faculties in Poland from dogs diagnosed with heart tumours between 1970 and 2014. The dogs’ age, breed and sex with tumour localisation and histopathological diagnosis were analysed. Because of its most common incidence, samples of haemangiosarcoma underwent further examination with assessment of the expr

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