Abstract
Haematologic patients are set apart by specific complications like immunosuppression, thrombocytopenia, sometimes associating coagulopathy and multiple points of entry for infection (central venous catheters and mucositis).
The right-sided heart is of particular importance in this type of patients as it is the preferred location of both primary and secondary cardiac tumours and is more frequently affected by radiation therapy due to its more anterior position in the thorax.
Chemotherapeutics may determine pulmonary hypertension and thus put a strain on the right ventricle.
Moreover, investigation of right-heart parameters like tricuspid annular plane systolic excursion and strain rate may reveal early cardiac dysfunction and establish prognosis in cardiac amyloidosis.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Notes
- 1.
The isointensity to normal myocardium on T1 and T2-weighted imaging and heterogeneity of enhancement on MRI are unique to PCL. Furthermore, MRI has the advantage of being able to differentiate between primary cardiac tumors: cardiac lipomas have high signal intensity on T1-weighted and intermediate signal on T2-weighted imaging (similar to mediastinal fat on MRI), fibromas have low signal intensity on T1 and T2 -weighted sequences (consistent with fibrous tissue), and pericardial cysts have low T1 signal intensity and high T2 signal intensity (as is the case with simple fluid).
- 2.
As lymphoma and breast and gastric cancer usually respond to similar chemotherapy regimens and/or radiation therapy, the two entities have most commonly been studied together.
References
Nikdoust F, Sani ZA, Tabatabaei SA. Right ventricle tumoral mass in acute promyelocytic leukemia (AML M3): cardiac magnetic resonance findings. Iranian Heart J. 2016;17(3):46–50.
Young J, Goldman IR. Tumor metastasis to the heart. Circulation. 1954;9(2):220–9.
Amano J, Nakayama J, Yoshimura Y, Ikeda U. Clinical classification of cardiovascular tumors and tumor-like lesions, and its incidences. Gen Thorac Cardiovasc Surg. 2013;61(8):435–47.
Goudie RB. Secondary tumours of the heart and pericardium. Br Heart J. 1955;17(2):183.
Laws JW, Annes GP, Bogren HG. Primary malignant tumors of the heart. Calif Med. 1973;118(4):11.
Mukai K, Shinkai T, Tominaga K, Shimosato Y. The incidence of secondary tumors of the heart and pericardium: a 10-year study. Jpn J Clin Oncol. 1988;18(3):195–201.
Hanfling SM. Metastatic cancer to the heart. Circulation. 1960;22(3):474–83.
Voigt P, Wienbeck S, Weber M-A, Oyama-Manabe N, Beimler M, Schob S, et al. Cardiac hematological malignancies: typical growth patterns, imaging features, and clinical outcome. Angiology. 2017;69(2):170–6. https://doi.org/10.1177/0003319717713581.
Barbaric D, Holley D, Lau K-C, McCowage G. It is ALL in the heart: a patient with acute lymphoblastic leukemia and cardiac infiltration at time of diagnosis. Leuk Lymphoma. 2002;43(12):2417–9.
Skhvatsabaja L. Secondary malignant lesions of the heart and pericardium in neoplastic disease. Oncology. 1986;43(2):103–6.
Perry DJ, McCormick D, Veasey S, Cohen IS. Right heart obstruction due to intracavitary prolymphocytic leukemia. Am J Med. 1986;81(1):131–4.
Dingerkus H, Völler H, Albrecht A, Hennig L, Stein H, Schröder R. Mediastinal chloroma affecting the right heart with superior vena cava syndrome. Am Heart J. 1994;127(2):465–8.
Makaryus AN, Tung F, Liu W, Mangion J, Kort S. Extensive neoplastic cardiac infiltration in a patient with acute myelogenous leukemia: role of echocardiography. Echocardiography. 2003;20(6):539–44.
Hunkeler N, Canter CE. Antemortem diagnosis of gross cardiac metastasis in childhood leukemia: echocardiographic demonstration. Pediatr Cardiol. 1990;11(4):225–6.
Foucar K, Foucar E, Willman C, Horvath A, Gerety RL. Nonleukemic granulocytic sarcoma of the heart: a report of a fatal case. Am J Hematol. 1987;25(3):325–32.
Marcos-Alberca P, Ibáñez B, Rey M, Román A, Rábago R, Orejas M, et al. Cardiac granulocytic sarcoma (chloroma): in vivo diagnosis with transesophageal echocardiography. J Am Soc Echocardiogr. 2004;17(9):1000–2.
Mawad R, Wu D, Abkowitz JL, Walter RB. Myeloid sarcoma of the heart. Leuk Lymphoma. 2012;53(12):2511–4.
Attallah A, Cheong BY, Bernicker E, Wilson JM. Cardiac chloroma: novel presentation and subsequent diagnosis with cardiac magnetic resonance imaging. Tex Heart Inst J. 2010;37(2):242.
Mignano JE, Chan MD, Rosenwald IB, Kimmelstiel CD, Wolfe LC. Intracardiac chloroma. J Pediatr Hematol Oncol. 2009;31(12):977–9.
Fernandez L, Couban S, Sy R, Miller R. An unusual presentation of extramedullary plasmacytoma occurring sequentially in the testis, subcutaneous tissue, and heart. Am J Hematol. 2001;67(3):194–6.
Singh B, Lahiri A, Kakar P. Extramedullary plasmacytoma. J Laryngol Otol. 1979;93(12):1239–44.
Knowling MA, Harwood AR, Bergsagel DE. Comparison of extramedullary plasmacytomas with solitary and multiple plasma cell tumors of bone. J Clin Oncol. 1983;1(4):255–62.
Keung Y, Lau S, Gill P. Extramedullary plasmacytoma of the heart presenting as cardiac emergency: review of literature. Am J Clin Oncol. 1994;17(5):427–9.
Nanjappa MC, Shankarappa RK, Kalpana SR, Bhat P, Moorthy N. Intracardiac thrombi in acute myeloid leukemia: an echocardiographic and autopsy correlation. Echocardiography. 2010;27(1):E4–8.
McAllister HA, Hall RJ, Cooley DA. Tumors of the heart and pericardium. Curr Probl Cardiol. 1999;24(2):59–116.
Roberts WC, Glancy DL, Devita VT. Heart in malignant lymphoma (Hodgkin's disease, lymphosarcoma, reticulum cell sarcoma and mycosis fungoides): a study of 196 autopsy cases∗. Am J Cardiol. 1968;22(1):85–107.
Curtsinger CR, Wilson MJ, Yoneda K. Primary cardiac lymphoma. Cancer. 1989;64(2):521–5.
Chalabreysse L, Berger F, Loire R, Devouassoux G, Cordier J-F, Thivolet-Bejui F. Primary cardiac lymphoma in immunocompetent patients: a report of three cases and review of the literature. Virchows Arch. 2002;441(5):456–61.
Petrich A, Cho SI, Billett H. Primary cardiac lymphoma. Cancer. 2011;117(3):581–9.
Gowda RM, Khan IA. Clinical perspectives of primary cardiac lymphoma. Angiology. 2003;54(5):599–604.
Nakayama Y, Uchimoto S, Tsumura K, Morii H. Primary cardiac lymphoma with infiltration of the atrioventricular node: remission with reversal of the atrioventricular block induced by chemotherapy. Cardiology. 1997;88(6):613–6.
Legault S, Couture C, Bourgault C, Bergeron S, Poirier P, Sénéchal M. Primary cardiac Burkitt-like lymphoma of the right atrium. Can J Cardiol. 2009;25(3):163–5.
Miguel CE, Bestetti RB. Primary cardiac lymphoma. Int J Cardiol. 2011;149(3):358–63.
Chim C, Chan A, Kwong Y, Liang R. Primary cardiac lymphoma. Am J Hematol. 1997;54(1):79–83.
Woods J, Monteiro P, Rhodes A. Right ventricular dysfunction. Curr Opin Crit Care. 2007;13(5):532–40.
Fortún J. Principales infecciones en el paciente oncológico: manejo práctico. An Sist Sanit Navar. 2004.
Chen K-W, Chang J-H, Yeh S-P, Lu C-R. Primary cardiac B-cell lymphoma with atrioventricular block and paroxysmal ventricular tachycardia. J Cardiothorac Surg. 2012;7(1):70.
Dorsay TA, Ho VB, Rovira MJ, Armstrong MA, Brissette MD. Primary cardiac lymphoma: CT and MR findings. J Comput Assist Tomogr. 1992;17(6):978–81.
Mügge A, Daniel WG, Haverich A, Lichtlen PR. Diagnosis of noninfective cardiac mass lesions by two-dimensional echocardiography. Comparison of the transthoracic and transesophageal approaches. Circulation. 1991;83(1):70–8.
Moore JA, DeRan BP, Minor R, Julie A, Fraker TD. Transesophageal echocardiographic evaluation of intracardiac lymphoma. Am Heart J. 1992;124(2):514–6.
Cho SW, Kang YJ, Kim TH, Cho SK, Hwang MW, Chang W, et al. Primary cardiac lymphoma presenting with atrioventricular block. Korean Circ J. 2010;40(2):94–8.
Ceresoli GL, Ferreri AJ, Bucci E, Ripa C, Ponzoni M, Villa E. Primary cardiac lymphoma in immunocompetent patients. Cancer. 1997;80(8):1497–506.
Nielsen KM, Offersen BV, Nielsen HM, Vaage-Nilsen M, Yusuf SW. Short and long term radiation induced cardiovascular disease in patients with cancer. Clin Cardiol. 2017;40(4):255–61.
Yusuf SW, Sami S, Daher IN. Radiation-induced heart disease: a clinical update. Cardiol Res Pract. 2011;2011:317659.
Tadic M, Cuspidi C, Hering D, Venneri L, Grozdic-Milojevic I. Radiotherapy-induced right ventricular remodelling: the missing piece of the puzzle. Arch Cardiovasc Dis. 2017;110(2):116–23.
Brosius FC, Waller BF, Roberts WC. Radiation heart disease: analysis of 16 young (aged 15 to 33 years) necropsy patients who received over 3,500 rads to the heart. Am J Med. 1981;70(3):519–30.
Burger A, Loffler H, Bamberg M, Rodemann HP. Molecular and cellular basis of radiation fibrosis. Int J Radiat Biol. 1998;73(4):401–8.
Taunk NK, Haffty BG, Kostis JB, Goyal S. Radiation-induced heart disease: pathologic abnormalities and putative mechanisms. Front Oncol. 2015;5:39.
Khakoo AY, Yeh ET. Therapy insight: management of cardiovascular disease in patients with cancer and cardiac complications of cancer therapy. Nat Clin Pract Oncol. 2008;5(11):655–68.
Torbey E, Yacoub H, McCord D, Lafferty J. Two cases and review of the literature: primary percutaneous angiography and antiplatelet management in patients with immune thrombocytopenic purpura. ISRN Hematol. 2013;2013:174659.
Slama MS, Guludec D, Sebag C, Leenhardt AR, Davy J, Pellerin DE, et al. Complete atrioventricular block following mediastinal irradiation: a report of six cases. Pacing Clin Electrophysiol. 1991;14(7):1112–8.
Gomez DR, Yusuf SW, Munsell MF, Welsh JW, Liao Z, Lin SH, et al. Prospective exploratory analysis of cardiac biomarkers and electrocardiogram abnormalities in patients receiving thoracic radiation therapy with high-dose heart exposure. J Thorac Oncol. 2014;9(10):1554–60.
Orzan F, Brusca A, Gaita F, Giustetto C, Figliomeni M, Libero L. Associated cardiac lesions in patients with radiation-induced complete heart block. Int J Cardiol. 1993;39(2):151–6.
Yeh ET, Tong AT, Lenihan DJ, Yusuf SW, Swafford J, Champion C, et al. Cardiovascular complications of cancer therapy. Circulation. 2004;109(25):3122–31.
Tadic M, Cuspidi C, Hering D, Venneri L, Danylenko O. The influence of chemotherapy on the right ventricle: did we forget something? Clin Cardiol. 2017;40(7):437–43.
Vejpongsa P, Yeh E. Topoisomerase 2β: a promising molecular target for primary prevention of anthracycline-induced cardiotoxicity. Clin Pharmacol Ther. 2014;95(1):45–52.
Lemez P. Delayed administration of dexrazoxane provides cardioprotection against anthracyclines in breast cancer or acute myeloid leukemia. J Clin Oncol. 1997;15(10):3293–5.
Sabatino J, Yauda M, De Rosa S, Tamme L, Ianconetti C, Albanese M, Mignona C, Aquila I, Donato G, Indolfi C. Empagliflozin reduces the doxorubicine-induced myocardial dysfunction. Eur Heart J. 2017. https://doi.org/10.1093/eurheartj/ehx504.P4230.
Kong JH, Jeon Y-W, Lee S-E, Choi SY, Kim S-H, Oh YJ, et al. Long-term assessment of Dasatinib-induced pulmonary arterial hypertension in chronic myeloid leukemia. Blood. 2014;124:5535.
Yun S, Anwer F, Vincelette ND. Dasatinib-induced pulmonary hypertension in chronic myelogenous leukaemia. BMJ Case Rep. 2014;2014:bcr2014204477.
Lenčová-Popelová O, Jirkovský E, Mazurová Y, Lenčo J, Adamcová M, Šimůnek T, et al. Molecular remodeling of left and right ventricular myocardium in chronic anthracycline cardiotoxicity and post-treatment follow up. PLoS One. 2014;9(5):e96055.
Murbraech K, Holte E, Broch K, Smeland KB, Holte H, Rösner A, et al. Impaired right ventricular function in long-term lymphoma survivors. J Am Soc Echocardiogr. 2016;29(6):528–36.
Christiansen JR, Massey R, Dalen H, Kanellopoulos A, Hamre H, Ruud E, et al. Right ventricular function in long-term adult survivors of childhood lymphoma and acute lymphoblastic leukaemia. Eur Heart J Cardiovasc Imaging. 2016;17(7):735–41.
Calleja A, Poulin F, Khorolsky C, Shariat M, Bedard PL, Amir E, et al. Right ventricular dysfunction in patients experiencing cardiotoxicity during breast cancer therapy. J Oncol. 2015;2015:609194.
Chan P, Ogilby JD, Segal B. Tricuspid valve endocarditis. Am Heart J. 1989;117(5):1140–6.
Chaudhary N, Vishwanath M, Pahuja M, Borker A. Candida albicans endocarditis in a child with acute lymphoblastic leukemia: a dreaded complication of intensive chemotherapy. Indian J Med Paediatr Oncol. 2013;34(1):28.
Nandakumar R, Raju G. Isolated tricuspid valve endocarditis in nonaddicted patients: a diagnostic challenge. Am J Med Sci. 1997;314(3):207–12.
Baddour LM, Wilson WR, Bayer AS, Fowler VG, Tleyjeh IM, Rybak MJ, et al. Infective endocarditis in adults: diagnosis, antimicrobial therapy, and management of complications. Circulation. 2015;132(15):1435–86.
Kantarcioglu B, Bekoz HS, Olgun FE, Cakal B, Arkan B, Turkoglu H, et al. Allogeneic stem cell transplantation in a blast-phase chronic myeloid leukemia patient with carbapenem-resistant Klebsiella pneumoniae tricuspid valve endocarditis: a case report. Mol Clin Oncol. 2016;5(4):347–50.
Barshay J, Nemets A, Ducach A, Lugassy G. Pseudomonas aeruginosa endocarditis in acute myeloid leukemia: a rare complication. Int J Biomed Sci. 2008;4(4):330.
Yong MS, Coffey S, Prendergast BD, Marasco SF, Zimmet AD, McGiffin DC, et al. Surgical management of tricuspid valve endocarditis in the current era: a review. Int J Cardiol. 2016;202:44–8.
Kuruvilla J, Forrest D, Lavoie J, Nantel S, Shepherd J, Song K, et al. Characteristics and outcome of patients developing endocarditis following hematopoietic stem cell transplantation. Bone Marrow Transplant. 2004;34(11):969.
Chrissoheris MP, Libertin C, Ali RG, Ghantous A, Bekui A, Donohue T. Endocarditis complicating central venous catheter bloodstream infections: a unique form of health care associated endocarditis. Clin Cardiol. 2009;32(12):E48–54.
Malagola M, Peli A, Damiani D, Candoni A, Tiribelli M, Martinelli G, et al. Incidence of bacterial and fungal infections in newly diagnosed acute myeloid leukaemia patients younger than 65 yr treated with induction regimens including fludarabine: retrospective analysis of 224 cases. Eur J Haematol. 2008;81(5):354–63.
Roguin A, Reisner S. Right atrial mass related to indwelling central venous catheters in patients undergoing dialysis. Eur J Echocardiogr. 2000;1(3):222–3.
Kale SB, Raghavan J. Tricuspid valve endocarditis following central venous cannulation: the increasing problem of catheter related infection. Indian J Anaesth. 2013;57(4):390.
Liepman MK, Jones PG, Kauffman CA. Endocarditis as a complication of indwelling right atrial catheters in leukemic patients. Cancer. 1984;54(5):804–7.
Kravitz MS, Shoenfeld Y. Thrombocytopenic conditions—autoimmunity and hypercoagulability: commonalities and differences in ITP, TTP, HIT, and APS. Am J Hematol. 2005;80(3):232–42.
Solomons P. Acute promyelocytic leukaemia associated with acute myocardial infarction-a case report. S Afr Med J. 1986;70(1):117–8.
Cappelli F, Porciani MC, Bergesio F, Perlini S, Attanà P, Moggi Pignone A, et al. Right ventricular function in AL amyloidosis: characteristics and prognostic implication. Eur Heart J Cardiovasc Imaging. 2011;13(5):416–22.
Kyle RA, Gertz MA. Primary systemic amyloidosis: clinical and laboratory features in 474 cases. Semin Hematol. 1995;32(1):45–59.
Hassan W, Al-Sergani H, Mourad W, Tabbaa R. Amyloid heart disease: new frontiers and insights in pathophysiology, diagnosis, and management. Tex Heart Inst J. 2005;32(2):178.
Falk RH, Comenzo RL, Skinner M. The systemic amyloidoses. N Engl J Med. 1997;337(13):898–909.
Child JS, Levisman JA, Abbasi AS, MacAlpin RN. Echocardiographic manifestations of infiltrative cardiomyopathy: a report of seven cases due to amyloid. Chest. 1976;70(6):726–31.
Lehtonen J, Kettunen P. Pulmonary hypertension as a dominant clinical picture in a case of amyloidosis and smoldering multiple myeloma. Int J Cardiol. 2007;115(1):E29–30.
Bellavia D, Pellikka PA, Dispenzieri A, Scott CG, Al-Zahrani GB, Grogan M, et al. Comparison of right ventricular longitudinal strain imaging, tricuspid annular plane systolic excursion, and cardiac biomarkers for early diagnosis of cardiac involvement and risk stratification in primary systematic (AL) amyloidosis: a 5-year cohort study. Eur Heart J Cardiovasc Imaging. 2012;13(8):680–9.
Klein AL, Hatle LK, Burstow DJ, Taliercio CP, Seward JB, Kyle RA, et al. Comprehensive Doppler assessment of right ventricular diastolic function in cardiac amyloidosis. J Am Coll Cardiol. 1990;15(1):99–108.
Griffiths B, Hughes P, Dowdle R, Stephens M. Cardiac amyloidosis with asymmetrical septal hypertrophy and deterioration after nifedipine. Thorax. 1982;37(9):711.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2018 Springer International Publishing AG, part of Springer Nature
About this chapter
Cite this chapter
Vintilă, AM., Horumbă, M., Vintilă, V.D. (2018). Right Heart Involvement in Haematologic Disorders. In: Dumitrescu, S., Ţintoiu, I., Underwood, M. (eds) Right Heart Pathology. Springer, Cham. https://doi.org/10.1007/978-3-319-73764-5_27
Download citation
DOI: https://doi.org/10.1007/978-3-319-73764-5_27
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-73763-8
Online ISBN: 978-3-319-73764-5
eBook Packages: MedicineMedicine (R0)