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Metastatic colorectal carcinoma to the right atrium: a case report and review of the literature

Abstract

Background

Cardiac metastasis due to colon cancer is extraordinarily uncommon. Given the rarity of diagnosis, there is paucity of evidence and hence, no established guidelines for evaluation or clinical management strategy.

Clinical presentation

We present the case of a 59 year old male with a previously treated colonic carcinoma who presented with new onset exertional dyspnea. He was noted to be having a right atrial mass on an echocardiogram performed at his cardiologist’s office. Further workup with CT angiogram of the chest confirmed a right atrial mass measuring 4.0 cm. Serum CEA was normal. Biopsies of the right atrial mass demonstrated metastatic moderately differentiated colonic adenocarcinoma. Mismatch repair protein expression analysis by immunohistochemistry showed no loss of MLH1, MSH2, MSH6 or PMS2 expression. Next generation sequencing for RAS and BRAF mutations was negative. Patient received treatment with FOLFIRINOX/ bevacizumab with noted reduction in size of mass.

Conclusion

To the best of our knowledge, this is the first report of next generation sequencing results available on a biopsy of metastatic colorectal cancer to the heart with the largest literature review of 31 reported cases of metastatic colorectal cancer to the heart. It will help direct clinical management and also adds evidence to the potential efficacy of treatment of this rare aggressive disease with chemotherapy in combination with VEGF inhibitors.

Introduction

Colorectal carcinoma is the third most common malignancy and the third most common cause of cancer deaths in both men and women in the United States [1]. The most common sites of metastasis of colorectal cancer are lymph nodes, liver and lungs, via lymphatic or hematogenous spread. Cardiac metastasis with colorectal cancer is rare, with very few cases reported in literature. Hence there is paucity of data regarding the best imaging modalities and treatment options for this condition.

Here we report a rare case of colorectal cancer metastatic to the heart, discovered 5 years after diagnosis and treatment of a primary colon cancer that responded remarkably to chemotherapy. We also provide the largest review of literature of cardiac metastases from colorectal carcinoma.

Case

A 59 year old male presented with a 2 week history of progressively worsening exertional dyspnea (NYHA class II), bilateral lower extremity edema and abdominal distension. He denied any fever, chills, chest pain, cough, orthopnea, paroxysmal nocturnal dyspnea, palpitations, nausea, vomiting, abdominal pain, syncope or weight loss. He presented to the Emergency Room after his cardiologist found a right atrial mass on echocardiogram during an office visit. His past medical history was significant for treated colorectal cancer, hyperlipidemia and gout.

The patient was diagnosed with colonic cancer 5.5 years earlier for which he underwent surgical resection with right hemicolectomy. The patient did not receive any adjuvant chemotherapy or radiation. He continued to follow up with his primary oncologist with surveillance CT scans and had completed his 5 year surveillance.

Family history was significant for colon cancer in his uncle and breast cancer in two of his sisters. He denied any tobacco use or alcohol intake.

The physical examination was remarkable for decreased lung sounds at the lung bases, moderate ascites and bilateral 1+ pitting edema up to the knees. EKG and cardiac enzymes were unremarkable. The patient underwent a CT angiogram of the chest which revealed a 4.0 cm low attenuating right atrial mass. The lung parenchyma had some ground-glass opacities bilaterally which were thought to be related to motion artefact or less likely suggestive of pulmonary edema. Deep venous thrombosis was ruled out with a negative lower extremity Doppler. The following day, he underwent paracentesis which showed a Serum Ascitis Albumin Gap of 1.4 and 726 nucleated cells (41% lymphocytes, 54% macrophages and 5% neutrophils). Cytologic examination was negative for malignancy, with findings notable for mesothelial cells and macrophages. Cardiac MRI showed a 8.3 cm × 6.5 cm right atrial mass extending from the suprarenal IVC into the hepatic veins and occupying the majority of the right atrium. The mass was noted to be isointense to myocardium on T1 weighted imaging, hyperintense to myocardium on T2 weighted imaging; with positive uptake of Gadolinium contrast in the peripheral segments of the tumor on first pass perfusion imaging, and had heterogeneous uptake on Late Gadolinium Enhancement imaging. A small circumferential pericardial effusion was also seen. Other laboratory studies were majorly unremarkable; with a normal CBC, CMP, PSA and serum CEA levels. The major differentials at this point were atrial myxoma, sarcoma or metastatic disease. It was believed that the shortness of breath was liked related to the increased right atrial pressures.

Cardiothoracic surgery performed an echocardiographic and fluoroscopic guided biopsy of the right atrial mass. The biopsy showed metastatic moderately differentiated colonic adenocarcinoma (Fig. 1). Mismatch repair protein expression analysis by immunohistochemistry showed no loss of MLH1, MSH2, MSH6 or PMS2 expression. No RAS, HRAS, NRAS or BRAF mutation was detected on next generation sequencing. MRI of the brain was negative for metastasis. However, MRI bone scan showed that the patient had a low T1 signal intensity in the left distal clavicle that was suspicious for metastatic disease. PET/ CT, was performed to evaluate if the disease was oligometastatic, confirmed metastatic disease in the left distal clavicle with a pathological fracture. The right atrial mass was also noted on PET/CT with abnormal uptake (SUV of 11). Treatment was initiated with plans for 4 cycles of FOLFIRINOX/ bevacizumab. Radiation therapy to the distal clavicle was deferred at this point pending response to chemotherapy.

Fig. 1
figure1

A: Metastatic moderately differentiated colonic adenocarcinoma with cribriform glandular growth pattern (H &E, ×100). B: Enteric differentiation demonstrated by strong immunohistochemical expression of CDX2. C: enteric differentiation demonstrated by strong immunohistochemical expression of cytokeratin 20(immunoperoxidase, × 100). D: negative cytokeratin 7 immunostaining (immunoperoxidase, × 100). Endomyocardium was not included in this spe cimen

Colonoscopy was performed during the hospitalization to rule out a second primary colorectal carcinoma. It showed a patent end to side ileo-colonic anastomosis with no endoscopic evidence of colon cancer was noted in the entire colon.

On his clinic visit to receive his second cycle of chemotherapy, he was noted to be doing much better with his symptoms of dyspnea and lower extremity edema being significantly better. However, he noted that the left clavicle was a little more painful, so oral opioids were added. At this point, radiation to the clavicle was planned. Repeat echocardiogram performed a month later showed a decrease in the size of the right atrial mass from 4 cm to 3 cm. On his most recent clinic visit, he continues to be asymptomatic and tolerated cycle 7 of chemotherapy with bevacizumab. A cardiac MRI is pending for him with plans to attempt surgical removal by the cardiothoracic surgery team if the tumor has regressed to the supra-diaphragmatic area.

Discussion

Cardiac metastasis are uncommon. Literature reviews for cardiac metastasis dating from 1948 to 2007 show that the incidence of cardiac metastasis ranges between 2.3–18.3% [2]. The highest incidence was noted by Hanfling in 1960 who reported an autopsy series comprising of 127 cases of cardiac metastasis in cancer patients with an incidence of 4.8% of all autopsies and 18.3% of all cancer related deaths. More recent studies from 2005 to 2007 show an incidence of 2.3–9.1%. An important consideration is that cardiac metastasis may be underestimated due to being clinically silent [2, 3]. The postulated mechanisms of cardiac metastasis include direct extension, hematogenous dissemination, lymphatic spread or by intra-cavitatary spread via the superior/ inferior vena cava. The highest rates of cardiac metastasis have been reported with pleural mesothelioma, melanoma and lung [2].

On our literature review, we found a total of 31 cases of metastatic cardiac involvement secondary to colorectal cancer. The patients ranged from 41 to 81 years with a median age of 70 years at diagnosis of metastasis. There is an overall male preponderance with 21 males vs 10 females reported thus far. Interval between initial diagnosis of malignancy and discovery of cardiac metastasis appears to be very wide. Upon literature review, the interval appears to extend unto 17 years after initial diagnosis of colorectal malignancy. Expert consensus regarding duration of surveillance for colorectal cancer per ASCO: American Society of Clinical Oncology, CCO: Cancer Care Ontario, NCCN: National Comprehensive Cancer Network ranges between roughly 3–5 years post initial diagnosis and treatment.

When symptomatic, cardiac metastases usually present with clinical features of heart failure including dyspnea, palpitations, thromboembolism or tumor extension into the superior or inferior vena cava manifesting with edema or obstructive signs [4, 5].

The differential to be considered when evaluating cardiac masses includes malignancies, atrial myxomas, thrombi and vegetations. Streptococcus gallolyticus infective endocarditis has been associated with colorectal malignancies. Various imaging modalities including transthoracic/ transesophageal echocardiography, CT or MRI can be utilized to provide a comprehensive view of the lesion and identify potentially infiltrative cardiac tumors. Molecular profiling of the metastatic tumor may help tailor the therapy and should be considered as part of the workup. Although colonoscopy is part of the initial workup for primary colon cancer; it should also be considered in patients who present with metastatic colorectal cancer to evaluate for a second primary colorectal carcinoma, as done for our patient. Henceforth, it would be plausible to consider further evaluation for cardiac involvement in any patient with a history of malignancy presenting with cardiopulmonary symptoms.

Metastatic cardiac tumors are generally associated with an aggressive disease course and a generally poor outcome. Only 9 out of the 31 reported cases of metastatic colorectal carcinoma to the heart were alive at the time of the case being reported. However, given the latest developments in diagnostic and therapeutic modalities, increased awareness and higher accessibility to health care over the years; it has become easier to identify these rare metastases.

In the event that an isolated metastasis or oligometastatic disease is found; multiple treatment options including surgical resection and chemotherapy may be offered. However, the ultimate decision would be contingent upon disease volume, tumor burden, comorbidities, genetic profiling and individualizing risk versus benefits for the patient. Surgery may be considered in a case of solitary cardiac metastasis or as a debulking maneuver if the lesion causes hemodynamic instability to bridge to ultimate treatment with chemotherapy. Upfront chemotherapy may be the best treatment for other patients. There is no consensus on treatment of cardiac metastasis and further studies are required to outline optimal treatment strategies for these patients.

Amongst the various treatment modalities that were used in the various cases reported; 14 patients underwent surgery only, 3 underwent chemotherapy only, 4 had surgery followed by chemotherapy, 9 received no treatment, treatment was not available for 2 of the reported cases.

Treatment with chemotherapy only in these patients with metastatic colorectal cancer lead to variable response to treatment but the patients invariably had ultimate disease progression or recurrence. Choufani et al. reported a case of patient who was 16 months post completion of treated metastatic colorectal cancer to the liver. This patient presented with new onset abdominal distension and dyspnea on exertion and was noted to be having a right atrial mass along with progression of liver metastases, new findings of ascites and pleural effusions. He received four doses of Irinotecan monthly with complete resolution of right atrial mass and ascites. However, subsequent CT scans showed partial recurrence of the right atrial mass and rising CEA levels. Overall, the patient was doing well symptomatically 10 months after resumption of irinotecan [6]. Pontillo et al. reported a case of Right atrial mass noted incidentally as part of pre-operative cardiac evaluation. This was noted 7 years following the patient’s previous diagnosis and treatment for CRC. She was also noted to be having peritoneal carcinomatosis and was treated with standard medical therapy. No specific names or duration of treatment was mentioned [7]. Meanwhile the case reported by Tsuji involved an incidentally diagnosed RV tumor with colonoscopy confirming wild type KRAS on histopathological examination. The tumor was deemed inoperable by surgeons and the patient was found to be having metastatic lung involvement as well. The patient received 10 cycles of 5-fluorouracil, oxaliplatin plus panitumumab. Oxaliplatin was held thereafter due to neuropathy and was deemed to be in partial response after 12 courses (10 months after initial treatment). However, follow up CT after 15 cycles showed progressive disease in the heart and the patient eventually elected for palliative care but was alive 2 years after his diagnosis [8].

Amongst the four cases with surgery followed by chemotherapy, two patients received bevacizumab-based treatments. Bianchi et al. reported a case with hyper-metabolic focus noted on PET/ CT in the Right Atrium following mildly elevated CEA levels at 35 ng/ml on routine surveillance 2 years out of treatment completion for colorectal cancer. Patient underwent a minimally invasive thoracotomy with mass excision which revealed the metastasis. The patient received 1 cycle of leucovorin, fluorouracil and irinotecan (FOLFIRI) and bevacizumab but was unable to tolerate subsequent sessions. Patient died 3 months later due to massive pulmonary embolism [9]. However, since the patient received only one cycle, it is uncertain to assess whether the patient could have had potential response to treatment. The patient reported by Butler et al. was noted to be having a mass in right atrioventricular groove on a CT scan/ TTE following elevated CEA levels 17 years following her initial diagnosis and treatment. The patient underwent cardiac surgery and resection. Follow up PET/ CT in 6 months after surgery showed extension of neoplastic disease in her left and right atria. Gene markers reportedly showed sensitivity to chemotherapy; however specifics regarding which markers were checked is not mentioned. The patient was treated with FOLFOX only initially; then bevacizumab was added. And 2.5 years since diagnosis of cardiac metastasis, she was placed on single agent bevacizumab without disease progression [10]. This case was similar to ours with regards to choice of treatment agents and response noted. In another case report by Namireddy et al., the patient presented with shortness of breath and syncope; 1 year after treatment for T3N1 rectal adenocarcinoma and was found to be having right atrial mass and moderate pulmonary embolism. The patient underwent median sternotomy with wide excision of the right atrial wall and was started on chemotherapy but no comments were noted with regards to the choice of the regimen or patient’s response to treatment [11]. de la Fouchardière et al. reported a patient who was 3.5 years post diagnosis for rectal cancer, the patient’s CEA levels were found to be up trending which prompted a PET/ CT scan which showed a 6 cm × 3 cm mass in the RV. The patient underwent cardiac surgery with palliative resection and subsequent pathology report revealed an adenocarcinoma confirming rectal origin. A post-operative CT scan showed residual intracardiac mass with pericardial effusion. He received 6 cycles of FOLFIRINOX after which the heart mass was noted to be stable and the pericardial effusion decreased. The patient completed a total of 11 cycles of FOLFOX. Patient asymptomatic throughout [12] (Table 1).

Table 1 Cardiac metastases from colorectal cancer. Review of the literature

Conclusion

Metastatic cardiac tumors have been linked with an aggressive disease course and poor outcomes in general. Given the recent developments in diagnostic and therapeutic modalities, integration of next generation sequencing; management options have evolved over the years for metastatic colorectal involvement of the heart. Hopefully, this literature review will help guide clinical management and also add to the evidence available. However, further studies are needed to formulate treatment strategies for this rare entity.

Availability of data and materials

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References

  1. 1.

    Siegel RL, Miller KD, Jemal A. Cancer statistics, 2020. CA A Cancer J Clin. 2020;70(1):7–30. https://doi.org/10.3322/caac.21590.

    Article  Google Scholar 

  2. 2.

    Bussani R, De-Giorgio F, Abbate A, Silvestri F. Cardiac metastases. J Clin Pathol. 2007;60(1):27–34. https://doi.org/10.1136/jcp.2005.035105 Epub 2006 Nov 10. PMID: 17098886; PMCID: PMC1860601.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  3. 3.

    Hanfling SM. Metastatic cancer to the heart. Review of the literature and report of 127 cases. Circulation. 1960;22(3):474–83. https://doi.org/10.1161/01.CIR.22.3.474.

    CAS  Article  PubMed  Google Scholar 

  4. 4.

    Patel SA, Herfel BM, Nolan MA. Metastatic colon cancer involving the right atrium. Tex Heart Inst J. 2012;39(1):79–83.

    PubMed  PubMed Central  Google Scholar 

  5. 5.

    Teixeira H, Timoteo T, Marcao I. Cardiac metastases from a colonic tumor [in Portuguese]. Acta Medica Port. 1997;10(4):331–4.

    CAS  Google Scholar 

  6. 6.

    Choufani EB, Lazar HL, Hartshorn KL. Two unusual sites of colon cancer metastases and a rare thyroid lymphoma. Case 2. Chemotherapy-responsive right atrial metastasis from colon carcinoma. J Clin Oncol. 2001;19(15):3574–5. https://doi.org/10.1200/JCO.2001.19.15.3574.

    CAS  Article  PubMed  Google Scholar 

  7. 7.

    Pontillo D, Zampi G, Pergolini A, Polizzi V, Tinti D, Spadaccia P. Cardiac metastasis from colorectal cancer: to be or not to be. Rev Port Cardiol. 2014;33(9):569–70. https://doi.org/10.1016/j.repc.2014.02.022.

    Article  PubMed  Google Scholar 

  8. 8.

    Tsujii Y, Hayashi Y, Maekawa A, Fujinaga T, Nagai K, Yoshii S, et al. Cardiac metastasis from colon cancer effectively treated with 5-fluorouracil, leucovorin, and oxaliplatin (modified FOLFOX6) plus panitumumab: a case report. BMC Cancer. 2017;17(1):152. https://doi.org/10.1186/s12885-017-3147-2.

    Article  PubMed  PubMed Central  Google Scholar 

  9. 9.

    Bianchi G, Cerillo AG, Murzi M, Solinas M. Surgical resection of colorectal carcinomas metastatic to the heart. J Card Surg. 2016;31(11):677–82. https://doi.org/10.1111/jocs.12841.

    Article  PubMed  Google Scholar 

  10. 10.

    Butler A, Wiebke EA. Cardiac recurrence in a patient with long-term survival from metastatic colon cancer. Case Rep Oncol. 2012;5(1):202–7. https://doi.org/10.1159/000338741.

    Article  PubMed  PubMed Central  Google Scholar 

  11. 11.

    Namireddy P, Alturi P, Alwair H, Cahill J, Muzaffar M. Cardiac metastasis as initial site of recurrence in rectal Cancer. Am J Med Sci. 2017;352(2):213–5.

    Article  Google Scholar 

  12. 12.

    de la Fouchardière C, Desseigne F, Orlandini F, et al. Cardiac metastases and colorectal cancer: a case study. Gastroentérol Clin Biol. 2007;31(6-7):621–3. https://doi.org/10.1016/S0399-8320(07)89443-7.

    Article  PubMed  Google Scholar 

  13. 13.

    Henuzet C, Franken P, Polis O, Fievez M. Cardiac metastasis of rectal adenocarcinoma diagnosed by two-dimensional echocardiography. Am Heart J. 1982;104(3):637–8. https://doi.org/10.1016/0002-8703(82)90240-X.

    CAS  Article  PubMed  Google Scholar 

  14. 14.

    Nishida H, Grooters RK, Coster D, Soltanzadeh H, Thieman KC. Metastatic right atrial tumor in colon cancer with superior vena cava syndrome and tricuspid obstruction. Heart Vessel. 1991;6(2):125–7. https://doi.org/10.1007/BF02058761.

    CAS  Article  Google Scholar 

  15. 15.

    Rutherford J, Sgroi D. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 45-1992. A 75-year-old man with carcinoma of the colon and a right ventricular mass. N Engl J Med. 1992;327(20):1442-8. https://doi.org/10.1056/NEJM199211123272007. PMID: 1328882.

  16. 16.

    Parravicini R, Fahim NA, Cocconcelli F, Barchetti M, Nafeh M, Benassi A, et al. Cardiac metastasis of rectal adenocarcinoma. Surgical treatment. Tex Heart Inst J. 1993;20(4):296–8.

    CAS  PubMed  PubMed Central  Google Scholar 

  17. 17.

    Testempassi E, Takeuchi H, Fukuda Y, Harada J, Tada S. Cardiac metastasis of colon adenocarcinoma diagnosed by magnetic resonance imaging. Acta Cardiol. 1994;49(2):191–6.

    CAS  PubMed  Google Scholar 

  18. 18.

    Zipoli A, Bartoli P, Fradella G, Sansoni M, Brandinelli A, Mazza F, et al. Right atrial metastasis as an initial clinical manifestation of adenocarcinoma of the colon. Ann Ital Med Int. 1994;9(3):150–2.

    CAS  PubMed  Google Scholar 

  19. 19.

    Lord RV, Tie H, Tran D, Thorburn CW. Cardiac metastasis from a rectal adenocarcinoma. Clin Cardiol. 1999;22:749.

    CAS  Article  Google Scholar 

  20. 20.

    Koizumi J, Agematsu K, Ohkado A, Shiikawa A, Uchida T. Solitary cardiac metastasis of rectal adenocarcinoma. Jpn J Thorac Cardiovasc Surg. 2003;51(7):330–2. https://doi.org/10.1007/BF02719389.

    Article  PubMed  Google Scholar 

  21. 21.

    Oneglia C, Negri A, Bonora-Ottoni D, Gambarotti M, Bisleri G, Rusconi C, et al. Congestive heart failure secondary to right ventricular metastasis of colon cancer. A case report and review of the literature. Ital Heart J. 2005;6(9):778–81.

    PubMed  Google Scholar 

  22. 22.

    Lui PCW, Wong RHL, Chu WCW, et al. Delayed right ventricular intracavitary metastasis in a patient with Dukes B rectal adenocarcinoma. Pathology. 2004;36:592–4.

    Article  Google Scholar 

  23. 23.

    Moreno-Vega AL, Fuentes-Pradera J, del Gordón-Santiago MM, Vargas-Machuca JC. Intraventricular metastases from rectal-sigmoid adenocarcinoma. Clin Transl Oncol. 2006;8(4):296–7. https://doi.org/10.1007/BF02664943.

    Article  PubMed  Google Scholar 

  24. 24.

    Choi PW, Kim CN, Chang SH, Chang WI, Kim CY, Choi HM. Cardiac metastasis from colorectal cancer: a case report. World J Gastroenterol. 2009;15(21):2675–8. https://doi.org/10.3748/wjg.15.2675.

    Article  PubMed  PubMed Central  Google Scholar 

  25. 25.

    Makhija Z, Deshpande R, Desai J. Unusual tumours of the heart: diagnostic and prognostic implications. J Cardiothorac Surg. 2009;4(1):4. https://doi.org/10.1186/1749-8090-4-4.

    Article  PubMed  PubMed Central  Google Scholar 

  26. 26.

    Ngow HA, Khairina WM. Cardiac mass in a patient with sigmoid adenocarcinoma: a metastasis? Cardiovasc J Afr. 2012;23(7):e10–2. https://doi.org/10.5830/CVJA-2012-027 Published 2012 Aug 12.

    Article  PubMed  Google Scholar 

  27. 27.

    Sudo Y, Enomoto Y. [Surgical management of metastatic colon cancer causing obstruction of the right ventricular outflow tract]. Kyobu geka. The Japanese Journal of Thoracic Surgery. 2013 Sep;66(10):907–10.

    PubMed  Google Scholar 

  28. 28.

    Mihali E, Mureşan M, Rusu ML, Fodor D. Cardiac metastasis and tumor embolism in a patient with adenocarcinoma of the colon presenting with paraneoplastic polymyositis. Romanian J Morphol Embryol. 2013;54(3 Suppl):897–900.

    CAS  Google Scholar 

  29. 29.

    Reisenauer JS, Said SM, Allen MS. Metastatic rectal adenocarcinoma presenting as a Giant left atrial mass: resection combined with right lower lobectomy. Ann Thorac Surg. 2016;102(1):e19–21. https://doi.org/10.1016/j.athoracsur.2015.11.064.

    Article  PubMed  Google Scholar 

  30. 30.

    Kasama K, Ichikawa Y, Suwa Y, Okudera K, Suzuki S, Masuda M. Late cardiac metastasis from colorectal carcinoma 15 years after surgery. Asian Cardiovasc Thorac Ann. 2016;24(1):66–8. https://doi.org/10.1177/0218492314539950.

    Article  PubMed  Google Scholar 

  31. 31.

    Ayyala SS, Urcuyo DM, Kannarkatt PT, Kovacs JE, Terrigno NJ. A rare case of atrial metastasis from a rectal adenocarcinoma. J Clin Med Res. 2017;9(10):886–8. https://doi.org/10.14740/jocmr3123w.

    Article  PubMed  PubMed Central  Google Scholar 

  32. 32.

    Elbatarny M, Butany J, Cusimano R. Late isolated metastasis of colon adenocarcinoma to the right ventricle. Hum Pathol: Case Rep. 2019;100287(16):1–3. https://doi.org/10.1016/j.ehpc.2019.01.006.

    Article  Google Scholar 

  33. 33.

    Graf A, Steffen C, Frick S. Spontaneous intracardiac microcavitations in a patient with a colonic carcinoma. BMJ Case Rep. 2019;12(9):e229932. https://doi.org/10.1136/bcr-2019-229932 Published 2019 Sep 5.

    Article  PubMed  PubMed Central  Google Scholar 

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No disclosures. The authors have no potential conflicts of interest involving the work submitted. No relevant financial disclosures. No relationships, affiliations or activities to disclose that could have influenced the submitted work.

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HS, AA analyzed and interpreted the patient data regarding the case. MD, MS performed the histological examination of the heart, and was a major contributor in writing the manuscript. KH supervised the entire data collection and manuscript writing process. All authors read and approved the final manuscript.”

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Correspondence to Humaira Sarfraz.

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Sarfraz, H., Arain, A., Divatia, M.K. et al. Metastatic colorectal carcinoma to the right atrium: a case report and review of the literature. Cardio-Oncology 7, 21 (2021). https://doi.org/10.1186/s40959-021-00108-9

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Keywords

  • Cardiac metastasis
  • Colon cancer
  • Next generation sequencing