Pediatric Cardiac Tumors

No Results

No Results


Cardiac tumors were first described in the 18th century by Boneti; however, many believe the description by Albers in 1835 is the first authentic report. In 1936, the first successful removal of a neoplasm of the heart was performed. In 1952, angiography was first used for the diagnosis of heart tumors. In 1955, bypass was used for the first time to excise an intracavitary tumor. Cardiac tumors, whether primary or metastatic, are rare. [1]

The image below demonstrates a large tumor in the left ventricular cavity of the heart.

Benign neoplasms occur 3 times more often than malignant tumors. By far, the most common type of tumors reported in children and adolescents is rhabdomyoma (see image below), followed by fibroma, myxoma, and teratoma. [2] is the largest group of primary cardiac malignant neoplasms. Of these sarcomas, angiosarcomas are the most common histologic type and occur more frequently in males. These tumors directly seed blood, thus metastases are common and widespread. Signs and symptoms of these tumors at presentation are generalized, nonspecific, and mimic several other systemic diseases.

The clinical presentation of a patient with a cardiac tumor is determined more by the tumor’s location than by its histologic type. Benign tumors, depending on their location, can present more symptoms than malignant tumors if they critically obstruct a valve or outflow tract. Consider the findings that are typical for each location.

Right-sided tumors may present with congestive heart failure (CHF) manifested by fatigue, edema, jugular venous distention, and ascites. Other symptoms include shortness of breath, syncope, and night sweats. Pericardial effusions may occur. Vena cava syndrome, pulmonary , and restrictive cardiomyopathy are some of the complications.

Left atrial and left ventricular tumors can present various signs and symptoms that include, but are not restricted to, fever, chills, dizziness, dyspnea on exertion, cold sweats during exercise or at night, and nonproductive cough. Because tumors may embolize, they also can lead to seizures, transient ischemic attacks, and cerebrovascular and peripheral-vascular accidents. Based on their size and position, they may induce arrhythmias and interfere with ventricular compliance.

Rhabdomyomas are hamartomas and are the most frequently found tumors in children as depicted in the images below. They are associated with tuberous sclerosis in about 50-80% of patients. Of patients with tuberous sclerosis, 50-60% have rhabdomyomas. These tumors are frequently multiple, involving ventricular and septal walls, and have a yellowish-gray . They vary from small to extremely large. They are rarely excised because they tend to regress over time; if patients are asymptomatic, only observation is warranted. Surgical removal is indicated when they present with obstruction leading to cardiac compromise or intractable arrhythmias. [3]

Fibromas, usually single and large, are most commonly found in the left ventricular wall and rarely involve the septal wall. As many as 40% of fibromas are diagnosed in infants younger than 1 year. These tend to be firm nonencapsulated tumors derived from fibroblasts.

Myxomas are usually seen in adults. They are rarely seen in children, accounting for only 9-15% of all cardiac tumors from birth to adolescence. They are often found attached to the atrial septum and mitral valve apparatus in the left atrium (>85%). Myxomas can appear sporadically or as part of the syndrome myxoma or Carney syndrome, which includes endocrine neoplasms, tumors in other organs, and skin with spotty hyperpigmentation. This type of familial cardiac myxoma accounts for less than 10% of the myxomas appearing in the heart. They have an autosomal dominant transmission and most commonly appear in females. Patients with syndrome myxoma tend to be younger than those with sporadic myxomas. Myxomas may embolize; this may be their first clinical presentation. Peripheral embolization is reported to occur in as many as 70% of patients with myxomas and may even occur in utero.

Teratomas are single, encapsulated, grayish-tan tumors that appear most often in the pericardium. Teratomas develop in the right atrium, right ventricle, and septum of the heart. They are large basal tumors that, in newborns, may be larger than the patient’s own heart.

Angiomas are a benign proliferation of endothelial cells, also known as vascular tumors. They can occur in any part of the heart (with a preference for right-sided chambers) and can form blood vessels (hemangiomas) or lymph vessels (lymphangiomas). These vascular vessels communicate between themselves within the myocardium. They can infiltrate the intraventricular septum near the conduction system where they may cause heart block. Hemangiomas are red, hemorrhagic, sessile, or polypoid subendocardial nodules that vary from small to large and occasionally have been associated with hemorrhagic cardiac tamponade.

Other types of tumors that have been less frequently reported in children include lipomas, papillary tumors, accessory cardiac cushion tissue, leiomyomas, mesotheliomas, fibroelastomas, fibroelastic papillomas, and benign cystic tumors.

Sarcomas originate from mesenchyme and, therefore, display a wide variety of morphologic types. These tumors are rare in children, with angiosarcoma being the most common type of for all ages.

Cardiac angiosarcomas are characteristically lobulated variegated masses that are necrotic or hemorrhagic and are composed of anastomosing vascular channels lined by malignant cells that may contain areas of spindle cells. They tend to be aggressive malignancies, either infiltrative or polypoid, with most arising from the right atrium. Metastases are common and, based on autopsy studies, occur in as many as 88% of patients with malignant tumors.

Rhabdomyosarcomas grow invasively, metastasize, and can recur. These tumors are rare and are more common in children because they may arise from embryonic cell rests in the septum.

Fibrosarcomas, often involving more than one chamber of the heart, contain areas of hemorrhage and necrosis.

Other reported malignant cardiac tumors are lymphomas, histiocytoma, leiomyosarcomas, choriocarcinoma, liposarcoma, and osteogenic sarcomas.

United States

Primary cardiac tumors are rare, with a frequency of 0.0017-0.28% based on autopsies. About 75% of them are benign and 25% are malignant. Secondary (metastatic) tumors are 10-40 times more frequent. Lam et al reviewed 12,485 autopsies and found only 7 cases of primary neoplasm of the heart versus 154 cases of secondary heart tumors. [4]

Rhabdomyomas are the most common tumor in children, with approximately 75% diagnosed in children younger than 1 year. Of these tumors, 50-80% are associated with tuberous sclerosis. Fibromas are the second most common tumor in children, with most (40%) diagnosed in children younger than 1 year. Myxomas are seen in 9-15% of patients with cardiac tumors, are the most common primary cardiac neoplasms in all ages, and comprise 50-60% of all heart tumors. The true incidence of teratomas is not known; however, 50% are diagnosed in newborns and 66% in children younger than 1 year. Sarcomas comprise 25% of all cardiac tumors; the most frequent tumor found is angiosarcoma.

No racial predilection is observed.

Myxomas are more common in females, especially in patients with syndrome myxoma or Carney syndrome. Angiosarcomas have a 2:1 male-to-female ratio. Rhabdomyomas, fibromas, teratomas, other sarcomas, and malignant tumors do not have any sex predilection.

No specific age predilection is noted; however, rhabdomyomas, fibromas, teratomas, and rhabdomyosarcomas are more commonly seen in children and adolescents than in adults. Myxomas comprise 50-60% of all benign tumors of the heart and are found mainly in adults.

Tao TY, Yahyavi-Firouz-Abadi N, Singh GK, Bhalla S. Pediatric cardiac tumors: clinical and imaging features. Radiographics. 2014 Jul-Aug. 34 (4):1031-46. [Medline].

Kutluk T, Demir HA, Buyukpamukcu M, et al. Cardiac rhabdomyomas in childhood: six cases from a single institution. Turk J Pediatr. 2013 Jan-Feb. 55(1):69-73. [Medline].

Nield LE, Mendelson M, Ahmad N, Manlhiot C, Jaeggi ET, McCrindle BW. Clinical Review of Obstructive Primary Cardiac Tumors in Childhood. Congenit Heart Dis. 2013 Aug 21. [Medline].

Lam KY, Dickens P, Chan AC. Tumors of the heart. A 20-year experience with a review of 12,485 consecutive autopsies. Arch Pathol Lab Med. 1993 Oct. 117(10):1027-31. [Medline].

Miyake CY, Del Nido PJ, Alexander ME, Cecchin F, Berul CI, Triedman JK, et al. Cardiac tumors and associated arrhythmias in pediatric patients, with observations on surgical therapy for ventricular tachycardia. J Am Coll Cardiol. 2011 Oct 25. 58(18):1903-9. [Medline].

Salpea P, Stratakis CA. Carney complex and McCune Albright syndrome: An overview of clinical manifestations and human molecular genetics. Mol Cell Endocrinol. 2013 Sep 5. [Medline].

Kono T, Koide N, Hama Y, et al. Expression of vascular endothelial growth factor and angiogenesis in cardiac myxoma: a study of fifteen patients. J Thorac Cardiovasc Surg. 2000 Jan. 119(1):101-7. [Medline].

Beroukhim RS, Prakash A, Buechel ER, Cava JR, Dorfman AL, Festa P, et al. Characterization of cardiac tumors in children by cardiovascular magnetic resonance imaging: a multicenter experience. J Am Coll Cardiol. 2011 Aug 30. 58(10):1044-54. [Medline].

Grant FD, Treves ST. Nuclear medicine and molecular imaging of the pediatric chest: current practical imaging assessment. Radiol Clin North Am. 2011 Sep. 49(5):1025-51. [Medline].

Amelia A, Mohd Nizam MB. Perinatal management of cardiac tumors: a case series. Med J Malaysia. 2013 Aug. 68(4):374-5. [Medline].

Linnemeier L, Benneyworth BD, Turrentine M, Rodefeld M, Brown J. Pediatric cardiac tumors: a 45-year, single-institution review. World J Pediatr Congenit Heart Surg. 2015 Apr. 6 (2):215-9. [Medline].

Butany J, Nair V, Naseemuddin A, et al. Cardiac tumours: diagnosis and management. Lancet Oncol. 2005 Apr. 6(4):219-28. [Medline].

Dhillon G, Rodriguez-Cruz E, Kathawala M, Alqassem N. Primary cardiac myofibroblastic sarcoma, case report and review of diagnosis and treatment of cardiac tumors. Bol Asoc Med P R. 1998 Jul-Dec. 90(7-12):130-3. [Medline].

Farooki ZQ, Ross RD, Paridon SM, et al. Spontaneous regression of cardiac rhabdomyoma. Am J Cardiol. 1991 Apr 15. 67(9):897-9. [Medline].

Gaumann A, Strubel G, Bode-Lesniewska B, Schmidtmann I, Kriegsmann J, Kirkpatrick CJ. The role of tumor vascularisation in benign and malignant cardiovascular neoplasms: a comparison of cardiac myxoma and sarcomas of the pulmonary artery. Oncol Rep. 2008 Aug. 20(2):309-18. [Medline].

Le Guyader A, Laskar M. Removal of left ventricular tumors by a transaortic transvalvular approach with the help of thoracoscopic instruments. J Thorac Cardiovasc Surg. 2008 Aug. 136(2):537-8. [Medline].

Lopez M, Pinto A, Moreno V, Diaz M, Gonzalez Baron A. Primary cardiac osteosarcoma. Clin Transl Oncol. 2008 Aug. 10(8):515-6. [Medline].

Ludomirsky A. Cardiac tumors. Bricker JT, Fisher DJ, eds. The Science and Practice of Pediatric Cardiology. 9th ed. Williams & Wilkins; 1998. Vol 2: 1885-93.

Martinez Quesada M, Trujillo Berraquero F, Almendro Delia M, et al. [Cardiac hamartoma. Case report and literature review]. Rev Esp Cardiol. 2005 Apr. 58(4):450-2. [Medline].

Marx GR. Cardiac Tumors. Emmanouilides GC, Gutgesell HP, Riemenschneider TA, Allen HD, eds. Moss and Adams Heart Disease in Infants, Children, and Adolescents: Including the Fetus and Young Adult. 5th ed. Baltimore, MD: Williams & Wilkins; 1995. Vol 2: 1773-86.

McAllister HA, Fenoglio JJ Jr. Tumors of the cardiovascular system: atlas of tumor pathology, second series. Washington, DC: Armed Forces Institute of Pathology. 1978.

Padalino MA, Basso C, Milanesi O, et al. Surgically treated primary cardiac tumors in early infancy and childhood. J Thorac Cardiovasc Surg. 2005 Jun. 129(6):1358-63. [Medline].

Piazza N, Chughtai T, Toledano K, et al. Primary cardiac tumours: eighteen years of surgical experience on 21 patients. Can J Cardiol. 2004 Dec. 20(14):1443-8. [Medline].

Rodriguez-Cruz E, Cintron-Maldonado RM, Bercu BA. Primary cardiac osteogenic sarcoma treated with heart transplantation. Bol Asoc Med PR. 1999. 91 (7-12):98-99. [Medline].

Rodriguez-Cruz E, Cintron-Maldonado RM, Forbes TJ. Treatment of primary cardiac malignancies with orthotopic heart transplantation. Bol Asoc Med P R. 2000 Apr-Aug. 92(4-8):65-71. [Medline].

Takach TJ, Reul GJ, Ott DA, Cooley DA. Primary cardiac tumors in infants and children: immediate and long-term operative results. Ann Thorac Surg. 1996 Aug. 62(2):559-64. [Medline].

Tatli S, Lipton MJ. CT for intracardiac thrombi and tumors. Int J Cardiovasc Imaging. 2005 Feb. 21(1):115-31. [Medline].

Tazelaar HD, Locke TJ, McGregor CG. Pathology of surgically excised primary cardiac tumors. Mayo Clin Proc. 1992 Oct. 67(10):957-65. [Medline].

Wu XM, Hu , Li N, et al. [Relationship of serum level of creatine kinase of MB type to cardiac function of patients with advanced tumors and its prognostic value]. Ai Zheng. 2005 Apr. 24(4):506-8.abs. [Medline].

Edwin Rodriguez-Cruz, MD Director, Section of Cardiology, Department of Pediatrics, San Jorge Children’s Hospital, Puerto Rico; Private Practice in Interventional Pediatric Cardiology and Internal Medicine, Centro Pedíatrico y Cardiovascular

Edwin Rodriguez-Cruz, MD is a member of the following medical societies: American College of Cardiology, American Heart Association, American Society of Echocardiography, Society for Cardiovascular Angiography and Interventions, Society of Pediatric Echocardiography, American College of Physicians-American Society of Internal Medicine, American Medical Association, Puerto Rico Medical Association

Disclosure: Serve(d) as a speaker or a member of a speakers bureau for: St Jude’s Medical Co.<br/>Received grant/research funds from NOVARTIS for investigator; Received consulting fee from St. Jude Medical Corp. for speaking and teaching.

Robert D Ross, MD Director of Pediatric Cardiology Fellowship Program, Department of Pediatrics, Division of Pediatric Cardiology, Children’s Hospital of Michigan; Professor of Pediatrics, Wayne State University School of Medicine

Robert D Ross, MD is a member of the following medical societies: American Academy of Pediatrics, American College of Cardiology, American Heart Association, Society of Pediatric Echocardiography

Disclosure: Nothing to disclose.

Mary L Windle, PharmD Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Nothing to disclose.

Ameeta Martin, MD Clinical Associate Professor, Department of Pediatric Cardiology, University of Nebraska College of Medicine

Ameeta Martin, MD is a member of the following medical societies: American College of Cardiology

Disclosure: Nothing to disclose.

Syamasundar Rao Patnana, MD Professor of Pediatrics and Medicine, Division of Cardiology, Emeritus Chief of Pediatric Cardiology, University of Texas Medical School at Houston and Children’s Memorial Hermann Hospital

Syamasundar Rao Patnana, MD is a member of the following medical societies: American Academy of Pediatrics, American Pediatric Society, American College of Cardiology, American Heart Association, Society for Cardiovascular Angiography and Interventions, Society for Pediatric Research

Disclosure: Nothing to disclose.

Jeffrey Allen Towbin, MD, MSc FAAP, FACC, FAHA, Professor, Departments of Pediatrics (Cardiology), Cardiovascular Sciences, and Molecular and Human Genetics, Baylor College of Medicine; Chief of Pediatric Cardiology, Foundation Chair in Pediatric Cardiac Research, Texas Children’s Hospital

Jeffrey Allen Towbin, MD, MSc is a member of the following medical societies: American Academy of Pediatrics, American Association for the Advancement of Science, American College of Cardiology, American College of Sports Medicine, American Heart Association, American Medical Association, American Society of Human Genetics, New York Academy of Sciences, Society for Pediatric Research, Texas Medical Association, Texas Pediatric Society, Cardiac Electrophysiology Society

Disclosure: Nothing to disclose.

Rosa M Cintrón-Maldonado, MD Clinical Instructor of Pediatrics, Department of Pediatrics, San Juan Bautista Medical Center

Rosa M Cintrón-Maldonado, MD is a member of the following medical societies: American Academy of Pediatrics

Disclosure: Nothing to disclose.

Pediatric Cardiac Tumors

Research & References of Pediatric Cardiac Tumors|A&C Accounting And Services

28 thoughts on “Pediatric Cardiac Tumors”

Leave a Reply