Vol 20, No 2 (2024)
Case report
Published online: 2023-10-17

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Cardiac metastasis of lung cancer diagnosed by fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography (18F-FDG PET/CT)

Yassir Benameur12, Salah Nabih Oueriagli1, Omar Ait Sahel1, Abderrahim Doudouh13
Oncol Clin Pract 2024;20(2):144-147.

Abstract

Lung cancer is currently one of the most common malignancies worldwide. Among all metastatic sites of this cancer, cardiac metastases are exceptional, and long-term prognosis in these patients is very poor. 18F-FDG PET/CT is a valuable imaging tool for initial staging and assessment of treatment response of various neoplasms. In the case of lung cancer, its role is clearly defined, and its effectiveness is superior to other diagnostic imaging methods. We present a rare 18F-FDG PET/CT image finding in a 71-year-old man with biopsy-proven lung squamous cell carcinoma, showing increased cardiac 18F-FDG uptake subsequently found to be compatible cardiac metastasis.

CASE REPORT

Oncology in Clinical Practice

DOI: 10.5603/ocp.95808

Copyright © 2024 Via Medica

ISSN 2450–1654

e-ISSN 2450–6478

Cardiac metastasis of lung cancer diagnosed by fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography (18F-FDG PET/CT)

Yassir Benameur12Salah Nabih Oueriagli1Omar Ait Sahel1Abderrahim Doudouh13
1Department of Nuclear Medicine, Mohammed V Military Teaching Hospital, Rabat, Morocco
2Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, Morocco
3Faculty of Medicine and Pharmacy, Mohammed V University, Rabat, Morocco

Address for correspondence:

Yassir Benameur, MD

Department of Nuclear Medicine,

Mohammed V Military Teaching Hospital

10045, Rabat, Morocco

e-mail: benameur.yassir@gmail.com

Received: 30.05.2023 Accepted: 18.08.2023 Early publication date: 17.10.2023

ABSTRACT

Lung cancer is currently one of the most common malignancies worldwide. Among all metastatic sites of this cancer, cardiac metastases are exceptional, and long-term prognosis in these patients is very poor. 18F-FDG PET/CT is a valuable imaging tool for initial staging and assessment of treatment response of various neoplasms. In the case of lung cancer, its role is clearly defined, and its effectiveness is superior to other diagnostic imaging methods.

We present a rare 18F-FDG PET/CT image finding in a 71-year-old man with biopsy-proven lung squamous cell carcinoma, showing increased cardiac 18F-FDG uptake subsequently found to be compatible cardiac metastasis.

Keywords: cardiac metastasis, FDG, lung cancer, PET/CT

Oncol Clin Pract 2024; 20, 2: 144147

Introduction

The most common metastatic sites in lung cancer are the nervous system, bones, liver, respiratory system, and adrenal glands [1]. Cardiac metastasis from lung cancer is rare and usually difficult to diagnose unless it causes symptoms. Most often it is discovered during assessment by fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography (18F-FDG PET/CT).

We describe a case of squamous cell lung carcinoma with metastasis to the right ventricle detected by FDG-PET/CT.

Case report

A 71-year-old man, a former smoker affected by arterial hypertension, presented with a cough, left chest pain, exertional breathlessness, and a weight loss of 10 kg in 4 months. Physical examination revealed reduced chest movements on the left anterior side of the chest and decreased intensity of breath sounds on auscultation. Computed tomography (CT) of the chest showed a large heterogeneous enhancing mass lesion measuring 6.7 cm × 7.2 cm × 7.4 cm with a spiculated margin in the lower lobe of the left lung. Computed tomography-guided biopsy confirmed the diagnosis of poorly differentiated squamous cell carcinoma. Fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography was performed to investigate potential metastases and, in addition to a hypermetabolic lung mass in the lower lobe (SUVmax = 14.3), it showed (1) lesions with increased FDG uptake in the left hilar and mediastinal lymph nodes and on the left iliac wing compatible with bone metastasis, (2) an intracardiac FDG-avid mass with SUVmax = 11.2 measuring 3.8 cm × 6.1 cm × 3.9 cm, suggesting a right ventricle metastasis.

The patient underwent transthoracic ultrasound and cardiac magnetic resonance imaging (CMR) for further evaluation and tissue characterization of the mass. Cardiac magnetic resonance imaging imaging showed a right ventricular mass, with high-signal intensity on T2-weighted imaging, hypoperfused on first-pass perfusion relative to the myocardium, and with late gadolinium hyperenhancement. These findings were consistent with the tumor diagnosis and likely represented metastatic disease.

Our patient was treated with palliative chemotherapy and died from general deterioration of his condition 6 months after the diagnosis.

Discussion

Heart tumors are rare and difficult-to-diagnose pathologies. Most primary cardiac tumors are benign in origin, and secondary cardiac tumors are more common than primary cardiac malignancies [2]. The incidence is higher than one may expect and ranges from 2.3% to 18.3% [3]. In theory, any cancer can lead to cardiac metastases. The most common cancers are melanoma, lung, breast, esophageal, and hematological malignancies [4]. These metastases are most often located in the right heart [5]. The myocardium is the most frequently metastatically affected cardiac tissue, followed by the pericardium and then the endocardium; conduction system involvement is much less common [6]. Metastasis can reach the heart through the dissemination of cancer cells into the bloodstream, or directly via adjacent tissues; another way is propagation via the superior or inferior vena cava to the right atrium [7]. In the case of lung cancer, metastatic cells often reach the heart through the lymphatic system; they usually do not cause any symptoms and are, therefore, rarely diagnosed before death [8].

The diagnosis of metastatic cardiac tumors is often delayed due to diverse and nonspecific manifestations, especially in early stages. In more advanced stages, secondary tumors of the heart gradually lead to heart failure, conduction disorders, valve diseases, such as mitral stenosis, angina pain, Adams-Stokes syndrome, and even sudden death. Such outcomes have been reported in approximately 3% of patients with cardiac metastases [9]. Electrocardiogram (ECG) changes are non-specific; in most cases, the ECG is normal. However, the following abnormalities may be observed: low voltage, ischemia, heart blocks, and arrhythmias [10]. Imaging studies have turned out to be very useful noninvasive tools for diagnostic evaluation of cardiac metastases. According to the 2022 European Society of Cardiology (ESC) Cardio-Oncology Guidelines, in the case of cardiac metastases, imaging can assess the possibility of heart surgery and may include echocardiography, CMR, computed tomography, and FDG-PET/CT [11]. Transthoracic echocardiography (TTE) or transesophageal echocardiography is the initial imaging test to detect cardiac metastases. It evaluates the size, location, mobility, and extent of pericardial invasion of the tumor [12]. Cardiovascular magnetic resonance adds information about tumor size, morphology, location, extent of invasion degree, and vascularity [13]. Fluorodeoxyglucose positron emission tomography/computed tomography provides a combination of data on tumor morphology and metabolism, which is relatively objective. Additionally, FDG-PET/CT features may be useful in distinguishing malignant and nonmalignant cardiac lesions, but this remains controversial [14].

Since histopathological confirmation of the cardiac metastases in our patient was not performed, we cannot completely rule out the possibility of other diseases. The differential diagnosis excluded cardiac thrombosis or the presence of a chemotherapy catheter [11] and included other causes of malignant or benign primary cardiac tumors. Most primary cardiac tumors are benign: myxomas, rhabdomyomas, papillary fibroelastoma, fibromas, hemangiomas, lipomas, and leiomyomas [15]. Cardiac sarcoma accounts for more than two-thirds of all primary cardiac malignant tumors, and histopathological subtypes of primary cardiac sarcoma include angiosarcoma, leiomyosarcoma, liposarcoma, rhabdomyosarcoma, synovial sarcoma, fibrosarcoma muscle and undifferentiated pleural sarcoma [16].

Figure 1. Fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography (18F-FDG PET/CT): maximum intensity projection maximum intensity projection (MIP) (A), and transaxial images of the thorax (B), showing an intense and pathological FDG uptake in the right ventricle (white arrow in MIP)

In our patient with aggressive lung cancer, the cardiac mass was considered secondary, and treatment was initiated.

In such cases, total surgical resection remains the treatment of choice, recommended in the 2022 ESC Cardio-Oncology Guidelines, but this option was not feasible due to high postoperative morbidity and the need for adjuvant radiotherapy or chemotherapy. Conventional radiotherapy is mainly used in palliative situations to bring relief to symptomatic patients [17].

The prognosis of patients with malignant cardiac tumors depends on many factors and, despite advances, remains generally poor, with survival ranging from 6 to ١٨ months after the diagnosis [18].

Conclusions

Our case demonstrates that FDG-PET/CT is an effective imaging modality for detecting rare distant metastatic sites, which can result in changing disease management. It increases chances of detecting cardiac metastases at an early stage thus facilitating adequate treatment.

Article Information and Declarations

Ethics statement

The patient's consent was obtained for the presentation of a clinical case.

Author contributions

Y.B.: article concept, writing, clinical data collection, literature data collection; S.N.O.: clinical data collection; O.A.S.: clinical data collection; A.D.: supervising and revising the article.

All authors have read and agreed to the published version of the manuscript.

Funding

None.

Acknowledgments

None.

Conflict of interest

Authors declare no conflict of interest.

Supplementary material

None.

References

  1. Riihimäki M, Hemminki A, Sundquist K, et al. The epidemiology of metastases in neuroendocrine tumors. Int J Cancer. 2016; 139(12): 26792686, doi: 10.1002/ijc.30400, indexed in Pubmed: 27553864.
  2. Paraskevaidis IA, Michalakeas CA, Papadopoulos CH, et al. Cardiac tumors. ISRN Oncol. 2011; 2011: 208929, doi: 10.5402/2011/208929, indexed in Pubmed: 22091416.
  3. Bussani R, De-Giorgio F, Abbate A, et al. Cardiac metastases. J Clin Pathol. 2007; 60(1): 2734, doi: 10.1136/jcp.2005.035105, indexed in Pubmed: 17098886.
  4. Murad R, Bakkar R, Sukkar R, et al. A Case of Ewing Sarcoma Presenting With Cardiac Metastasis. World J Pediatr Congenit Heart Surg. 2019; 10(5): 632634, doi: 10.1177/2150135119846047, indexed in Pubmed: 31496409.
  5. Reynen K, Köckeritz U, Strasser RH. Metastases to the heart. Ann Oncol. 2004; 15(3): 375381, doi: 10.1093/annonc/mdh086, indexed in Pubmed: 14998838.
  6. Shehata BM, Thomas JE, Doudenko-Rufforny I. Metastatic carcinoid to the conducting system-is it a rare or merely unrecognized manifestation of carcinoid cardiopathy? Arch Pathol Lab Med. 2002; 126(12): 15381540, doi: 10.5858/2002-126-1538-MCTTCS, indexed in Pubmed: 12456219.
  7. Lahmidi I, Assoweh CD, Haddiya I, et al. Clinicopathological features of adult right-sided cardiac masses: Analysis of 19 cases. Ann Med Surg (Lond). 2022; 77: 103613, doi: 10.1016/j.amsu.2022.103613, indexed in Pubmed: 35638074.
  8. Das A, Das SK, Pandit S, et al. Bronchogenic Carcinoma with Cardiac Invasion Simulating Acute Myocardial Infarction. Case Rep Oncol Med. 2016; 2016: 7813509, doi: 10.1155/2016/7813509, indexed in Pubmed: 27042370.
  9. Ito T, Ishikawa N, Negishi T, et al. Cardiac metastasis of tongue cancer may cause sudden death. Auris Nasus Larynx. 2008; 35(3): 423425, doi: 10.1016/j.anl.2007.04.017, indexed in Pubmed:
    17855031.
  10. Lyon AR, López-Fernández T, Couch LS, et al. ESC Scientific Document Group. 2022 ESC Guidelines on cardio-oncology developed in collaboration with the European Hematology Association (EHA), the European Society for Therapeutic Radiology and Oncology (ESTRO) and the International Cardio-Oncology Society (IC-OS). Eur Heart J. 2022; 43(41): 42294361, doi: 10.1093/eurheartj/ehac244, indexed in Pubmed: 36017568.
  11. Burazor I, Aviel-Ronen S, Imazio M, et al. Metastatic cardiac tumors: from clinical presentation through diagnosis to treatment. BMC Cancer. 2018; 18(1): 202, doi: 10.1186/s12885-018-4070-x, indexed in Pubmed: 29463229.
  12. Bogren HG, DeMaria AN, Mason DT. Imaging procedures in the detection of cardiac tumors, with emphasis on echocardiography: a review. Cardiovasc Intervent Radiol. 1980; 3(3): 107125, doi: 10.1007/BF02552329, indexed in Pubmed: 6991115.
  13. Yin H, Mao W, Tan H, et al. Role of F-FDG PET/CT imaging in cardiac and pericardial masses. J Nucl Cardiol. 2022; 29(3): 12931303, doi: 10.1007/s12350-020-02510-9, indexed in Pubmed: 33462788.
  14. Dos Santos VM, Dos Santos LA. Cardiac and lymphatic metastases from lung cancer. Arch Iran Med. 2018; 21(2): 8283, indexed in Pubmed: 29664660.
  15. Tyebally S, Chen D, Bhattacharyya S, et al. Cardiac Tumors: State-of-the-Art Review. JACC CardioOncol. 2020; 2(2): 293311, doi: 10.1016/j.jaccao.2020.05.009, indexed in Pubmed: 34396236.
  16. Chen TWW, Loong HH, Srikanthan A, et al. Primary cardiac sarcomas: A multi-national retrospective review. Cancer Med. 2019; 8(1): 104110, doi: 10.1002/cam4.1897, indexed in Pubmed: 30575309.
  17. Jumeau R, Vincenti MG, Pruvot E, et al. Curative management of a cardiac metastasis from lung cancer revealed by an electrical storm. Clin Transl Radiat Oncol. 2020; 21: 6265, doi: 10.1016/j.ctro.2019.10.005, indexed in Pubmed: 31993511.
  18. Bussani R, Castrichini M, Restivo L, et al. Cardiac Tumors: Diagnosis, Prognosis, and Treatment. Curr Cardiol Rep. 2020; 22(12): 169, doi: 10.1007/s11886-020-01420-z, indexed in Pubmed: 33040219.