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      Primary cardiac B-cell lymphoma involving sinus node, presenting as sick sinus syndrome

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          Abstract

          Introduction Sick sinus syndrome generally occurs in elderly patients. Two major causes for sick sinus syndrome are fibrosis of the sinus node and surrounding atrial myocardium and external causes to suppress the sinus node function. Fibrosis is mainly age-related, but can be caused by surgery, infiltrative diseases, or congenital disorders. We experienced a patient who presented with sick sinus syndrome and rapidly developed superior vena cava (SVC) syndrome shortly after the pacemaker implant. Autopsy showed B-cell lymphoma destroying the sinus node structure, which was thought to be the cause of sinus node dysfunction. Case report A 96-year-old woman without previous medical history presented with recurrent syncope at our hospital. Significant offset pause from atrial fibrillation up to 7 seconds and sinus bradycardia were noted, and she was diagnosed with sick sinus syndrome. Transthoracic echocardiography demonstrated no significant findings (Figure 1A). A single-chamber pacemaker was implanted without technical difficulty or complication, and she was discharged to a nursing home. At 1-month follow-up visit, she complained of anorexia and general malaise, and physical examination showed the swelling of the face, neck, and upper extremity. A chest radiograph revealed massive pleural effusion. Echocardiography showed a poorly mobile mass that partially occupied a right atrium (Figure 1B). Computed tomography with contrast showed an 8-cm mass extending from the high lateral right atrium to the SVC (Figure 2). She was diagnosed with SVC syndrome. Cytology of the pleural effusion showed no malignancy. The patient and her family chose the palliative care, and she died after 2 months. Figure 1 Echocardiogram pre- and 1 month post-implant. A: Baseline echocardiogram prior to the implant. No significant finding was found. B: Abnormal large mass in the right atrium. Figure 2 Three-dimensional computed tomography of the heart. Abnormal tumor in the right atrium is depicted with purple, which fills the upper part of the right atrium. Autopsy findings showed that the 8-cm tumor infiltrated from a right atrium to the pericardium, SVC, and right upper and middle lobes of the lung. The tumor extended to the right atrial appendage and crista terminalis (Figure 3A). Pathologic findings showed diffusely infiltrated lymphocytes with extreme nuclear atypia and lack of cell junction. Immunochemical staining showed positive CD20 (B-cell marker) and CD79a with negative CD3 (T-cell marker) and CD5. Pathologic findings confirmed the diagnosis of diffuse large B-cell lymphoma. Macroscopic examination and microscopic analysis showed the crista terminalis and sinoatrial node structure including the sinus node artery were completely destroyed owing to the massive infiltration by lymphoma (Figure 3B). Figure 3 Gross pathology of the heart and pathologic section of sinoatrial node. A: Abnormal tumor (arrow) extends from the right atrial appendage to the crista terminalis. Right atrium inflow from superior vena cava was stenosed by tumor. ATL = anterior tricuspid leaflet; CS = coronary sinus; CT = crista terminalis; OF = oval fossa; PTL = posterior tricuspid leaflet; RAA = right atrial appendage; RV = right ventricle; STL = septal tricuspid leaflet; TA = tricuspid annulus. B: Sinoatrial node structure that had been completely destroyed by lymphoma and pectinate muscle without infiltration. Discussion Metastatic malignant cardiac tumor is observed in 2.3% of all autopsy cases in general populations, 7.1% in cancer patients, and 24% in malignant lymphoma. 1 , 2 In contrast, primary cardiac tumor represents 0.33% of autopsies in general populations. 3 Especially, primary cardiac lymphoma is extremely rare, accounting for 1.3% of primary cardiac tumor. 4 Primary cardiac lymphoma was defined as a single cardiac disease and asymptomatic extracardiac site of disease or minimal locoregional disease. 5 We diagnosed our case as primary cardiac lymphoma, based on the major lesion in the right atrium, which extended to the epicardium, SVC, adjacent right lung, and mediastinal fat with asymptomatic, minimally disseminated lesions. As malignant lymphoma often presents with rapid progression, delayed diagnosis is the major factor associated with its poor prognosis. In this case, echocardiography showed rapidly expanding low echogenicity mass over 4 weeks. Common symptoms include heart failure, pericardial effusion, atrioventricular block, SVC syndrome, and precordial pain, but there have been few cases of sick sinus syndrome in previous reports.6, 7, 8 Our patient presented with sick sinus syndrome and developed SVC syndrome, caused by the rapidly grown B-cell malignant lymphoma. Conclusions We report an elderly woman who presented with sick sinus syndrome, which was caused by rapidly growing primary cardiac B-cell lymphoma. Key Teaching Points • Sick sinus syndrome in elderly patients is usually caused by fibrosis of sinus node and surrounding atrial myocardium or external causes to suppress the sinus node function. In rare occasions, it can be caused by primary cardiac lymphoma. • Cardiac malignancies are a rare disease and delayed diagnosis can lead to a poor prognosis. • It is useful to repeat echocardiography or computed tomography after the pacemaker implant in suspected patients.

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          Most cited references8

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          Cardiac metastases.

          We report a case of esophageal cancer with symptomatic metastases to the heart; the patient was treated with short-course radiotherapy with good symptomatic relief. We reviewed the current literature regarding the epidemiology, clinical presentation, diagnostic tools, treatment modalities, and the prognosis of cardiac metastases. In this report we summarize the most recent autopsy studies (published between 1975 and 2007), in which we found an autopsy incidence of cardiac metastases of 2.3% among the general population, while the incidence among autopsies of cancer patients was 7.1%. Therefore, we share the opinion with others that there has been an increase in the incidence of cardiac metastases among cancer patients diagnosed after 1970, in comparison with the reported incidences in older series before 1970 (7.1% vs 3.8%; Kruskal-Wallis rank test; P = 0.039). Special attention was given to the role of radiotherapy in the management of cardiac metastases.
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            Primary cardiac lymphoma in immunocompetent patients: diagnostic and therapeutic management.

            Primary cardiac lymphoma (PCL) is extremely rare in immunocompetent patients. Different definition criteria have been employed in published series. Prognosis is poor due to diagnostic delay and relevance of the site of disease. Two cases observed at the study institution are reported, with a review of 48 cases published in the literature from 1980 to 1996. Only patients with lymphoma confined to the heart and/or pericardium and those with a single and asymptomatic extracardiac site were considered for analysis. Eight patients had minimal extracardiac disease. The most common presentation was unresponsive heart failure. Electrocardiography findings were not specific. PCL usually arose in the right chambers as a mass, with or without pericardial effusion (> 80%). Chest X-rays, transthoracic echocardiography, and computed tomography scans are standard in diagnostic workup, but transesophageal echocardiography (TEE) and magnetic resonance imaging (MRI) showed a sensitivity > 90%. Cytology of pericardial effusion was diagnostic in 67% of cases. Thoracotomy was diagnostic in all cases, whereas less invasive procedures had high false-negative rates. Gross resection has no role. Early anthracycline-containing chemotherapy appears to improve survival, whereas the role of radiotherapy has not yet been defined. The diagnosis of PCL should be considered in patients with a cardiac mass and/or unexplained refractory pericardial effusion. Adequate diagnostic workup, including TEE and MRI, allows confirmation of the early suspicion of PCL. In the absence of a diagnostic cytology, an open biopsy may be indicated to avoid treatment delay. There is no evidence that PCL should be treated differently from other bulky aggressive lymphomas arising at other anatomic sites.
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              Heart in malignant lymphoma (Hodgkin's disease, lymphosarcoma, reticulum cell sarcoma and mycosis fungoides). A study of 196 autopsy cases.

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                Author and article information

                Contributors
                Journal
                HeartRhythm Case Rep
                HeartRhythm Case Rep
                HeartRhythm Case Reports
                Elsevier
                2214-0271
                27 June 2020
                October 2020
                27 June 2020
                : 6
                : 10
                : 694-696
                Affiliations
                []Department of Cardiology, Kyorin University Hospital, Tokyo, Japan
                []Department of Cardiology, Nihon Medical University Hospital, Tokyo, Japan
                []Department of Pathology, Kyorin University Hospital, Tokyo, Japan
                Author notes
                [] Address reprint requests and correspondence: Dr Kyoko Soejima, Cardiology, Kyorin University Hospital, 6-20-2 Shinkawa, Mitaka, Tokyo 181-8611, Japan. skyoko@ 123456ks.kyorin-u.ac.jp
                Article
                S2214-0271(20)30136-6
                10.1016/j.hrcr.2020.06.020
                7573383
                33101934
                b3b95827-a47e-4e87-84b1-15332cdd802f
                © 2020 Heart Rhythm Society. Published by Elsevier Inc.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                Categories
                Case Report

                autopsy,b-cell lymphoma,cardiac lymphoma,pacemaker,sick sinus syndrome

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