Case Reports in Medicine

Case Reports in Medicine / 2016 / Article

Case Report | Open Access

Volume 2016 |Article ID 9653412 | 6 pages |

Sanguineous Pericardial Effusion and Cardiac Tamponade in the Setting of Graves’ Disease: Report of a Case and Review of Previously Reported Cases

Academic Editor: Grigrios Korosoglou
Received20 Mar 2016
Accepted05 Jun 2016
Published29 Jun 2016


Introduction. Pericardial effusion in the setting of hyperthyroidism is rare. We present a patient with Graves’ disease who developed a sanguineous pericardial effusion and cardiac tamponade. Case Description. A 76-year-old man presenting with fatigue was diagnosed with Graves’ disease and treated with methimazole. Two months later, he was hospitalized for uncontrolled atrial fibrillation. Electrocardiography showed diffuse low voltage and atrial fibrillation with rapid ventricular rate. Chest radiograph revealed an enlarged cardiac silhouette and left-sided pleural effusion. Thyroid stimulating hormone was undetectable, and free thyroxine was elevated. Diltiazem and heparin were started, and methimazole was increased. Transthoracic echocardiography revealed a large pericardial effusion with cardiac tamponade physiology. Pericardiocentesis obtained 1,050 mL of sanguineous fluid. The patient progressed to thyroid storm, treated with propylthiouracil, potassium iodine, hydrocortisone, and cholestyramine. Cultures and cytology of the pericardial fluid were negative. Thyroid hormone markers progressively normalized, and he improved clinically and was discharged. Discussion. We found 10 previously reported cases of pericardial effusions in the setting of hyperthyroidism. Heparin use may have contributed to the sanguineous nature of our patient’s pericardial effusion, but other reported cases occurred without anticoagulation. Sanguineous and nonsanguineous pericardial effusions and cardiac tamponade may be due to hyperthyroidism.

1. Introduction

Hyperthyroidism is found in 1.3% of the United States population (12 years and older), and cardiac manifestations are common [1]. However, of those cardiac findings, pericardial effusion associated with hyperthyroidism has rarely been reported, limited to a small number of case reports primarily in the setting of Graves’ disease [28]. We report a patient with Graves’ disease and hyperthyroidism who developed a sanguineous pericardial effusion with cardiac tamponade. We reviewed the literature for previous case reports of patients with hyperthyroidism and pericardial effusion.

2. Case Description

A 76-year-old diabetic man presented to an outpatient clinic with fatigue. He was found to have a total thyroxine (T4) of 22.5 μg/dL (normal 4.5–12.1 μg/dL) and an undetectable thyroid stimulating hormone (TSH) (normal 0.358–3.740 IUI/mL). Diagnostic studies for hyperthyroidism found a thyroglobulin antibody of <20 IU/mL (normal < 40 IU/mL), thyroid peroxidase antibody of 17.0 IU/mL (normal < 35 IU/mL), thyroid stimulating immunoglobulin of 490% (normal ≤ 122%), thyroid stimulating hormone receptor antibody of 3.91 IU/L (normal ≤ 1.75 IU/L), 24-hour radioactive iodine-123 uptake of 45% (normal 10–30%) (Figure 1), and multiple smaller-than-one-centimeter thyroid nodules via an ultrasound of the thyroid. Physical examination did not find ophthalmopathy or dermopathy. He was diagnosed with Graves’ disease for which he was started on methimazole 10 mg daily. Over the next two months, he developed dyspnea on exertion, insomnia, fevers, night sweats, productive cough, and weight loss. He presented back to the clinic in atrial fibrillation with rapid ventricular rate and was admitted to the hospital.

On the day of admission, conventional chest radiography found an enlarged cardiac silhouette, bibasilar opacities, and left-sided pleural effusion (Figure 2). Cardiac markers included N-terminal prohormone of brain natriuretic peptide of 1,172 pg/mL (normal 0–450 pg/mL) and two-consecutive troponin I < 0.017 ng/mL (normal 0–0.059 ng/mL). Thyroid hormone levels were TSH of 0.007 UIU/mL (normal 0.358–3.740 IUI/mL), free T4 3.7 ng/dL (normal 0.7–1.6 ng/dL), total T4 21.3 μg/dL (normal 4.5–12.1 μg/dL), and free triiodothyronine 235 ng/dL (normal 55–172 ng/dL). Electrocardiography showed diffuse low voltage and was consistent with atrial fibrillation with rapid ventricular rate. Methimazole was increased to 30 mg daily. He was started on continuous diltiazem infusion (the patient had an allergy to beta blockers), continuous heparin infusion for atrial fibrillation, and ceftriaxone and azithromycin for possible community-acquired pneumonia.

On hospital day 1, transthoracic echocardiography (TTE) found a pericardial effusion (Figure 3), mitral wave flow variation of greater than 30%, mild right ventricular diastolic compression, and plethoric inferior vena cava with minimal reactivity. With continuous heparin infusion being discontinued shortly before the procedure, pericardiocentesis with the placement of a pericardial drain drained 850 mL of sanguineous fluid during the procedure, and 200 mL of fluid was drained during the subsequent day. Studies of the pericardial fluid found 607,000 red blood cells (RBCs), 4,548 total nucleated cells, 49% neutrophils, 15% lymphocytes, 36% mononuclear cells, 0% eosinophils, 0% other cells, 0% nucleated cells, glucose of 121 mg/dL (no reference range), lactate dehydrogenase (LDH) of 1,326 units/L (no reference range), specific gravity of 1.030 (no reference range), and total protein of 4.8 g/dL (no reference range). On that subsequent day, continuous diltiazem infusion was transitioned to oral diltiazem and he began aspirin.

On hospital day 3, he experienced worsening dyspnea, fever, and diarrhea consistent with thyroid storm, for which he received propylthiouracil potassium iodide, hydrocortisone, and cholestyramine. A left-sided thoracentesis was performed for increasing dyspnea and oxygen requirement and drained 1,250 mL of serous fluid. Studies of the pleural fluid found 1,000 RBCs, 364 total nucleated cells, 30% neutrophils, 44% lymphocytes, 26% mononuclear cells, 0% eosinophils, 0% other cells, 0% nucleated red blood cells, glucose of 140 mg/dL (no reference range), LDH of 78 units/L (no reference range), pH of 7.432 (no reference range), and total protein of 2.6 g/dL (no reference range). Studies were consistent with transudative effusion by Light’s criteria. On hospital day 5, the pericardial drain was removed, and TTE two days later showed trivial pericardial effusion. Cultures of the blood, pericardial fluid, pleural fluid, and sputum had no growth. Cytology of the pericardial fluid did not find malignant cells. He converted spontaneously to sinus rhythm and was discharged on methimazole 30 mg orally daily, hydrocortisone 15 mg orally every morning and 10 mg orally every evening, diltiazem 240 mg orally daily, and aspirin 81 mg orally daily. At follow-up clinic visits six weeks and five months later, he was asymptomatic, free T4 was normal, and ECG revealed sinus rhythm and normalization of voltage.

3. Discussion

Pericardial effusions occur in approximately 3% to 6% of patients with hypothyroidism [9]. Contrastingly, in our review of the literature, we found only 10 previously reported cases of pericardial effusion in the setting of hyperthyroidism (Table 1). Four of the pericardial effusions were sanguineous [2, 5, 7, 8]. Similar to our patient, six of the patients had Graves’ disease [2, 3, 7, 8]. Five of the 10 reported patients had atrial fibrillation [2, 68]. Our patient’s constellation of sanguineous pericardial effusion and atrial fibrillation treated with continuous heparin infusion appears unique among the available case reports, and the heparin may have contributed to the blood in our patient’s pericardial effusion.

ReferenceAge (years), genderEtiology of thyroid diseasePresence of tamponadePresence of atrial fibrillationSanguineous pericardial effusionCardiac intervention

Clarke et al. [2]53, maleNSYes, by clinical featuresNSYesPericardiocentesis, pericardiectomy
Clarke et al. [2]35, femaleGraves’ diseaseYes, by clinical featuresNSNSPericardiocentesis
Clarke et al. [2]54, femaleNSNo, by ECHOYesDescribed as “unremarkable”Pericardial biopsy
Clarke et al. [2]47, femaleGraves’ diseaseNo, by ECHOYesNSNone
Khalid et al. [3]68, femaleGraves’ diseaseNo, by ECHONSNSNone
Levy et al. [4]NS, NSNSNSNSNSNS
Nakata et al. [5]43, maleGraves’ diseaseNo, by ECHONoYesPericardiocentesis
Ovadia et al. [6]76, femaleMultinodular goiterNo, by ECHOYesNSNone
Teague et al. [7]42, femaleGraves’ diseaseYes, by ECHOYesYesPericardiocentesis
Yu et al. [8]33, femaleGraves’ diseaseYes, by ECHOYesYesPericardiocentesis
Current case76, maleGraves’ diseaseYes, by ECHOYesYesPericardiocentesis

ECHO: echocardiography; NS: not stated in case report.

The mechanism for the development of a pericardial effusion with Graves’ disease has not been elucidated. Previous authors have postulated that the mechanism is similar to that of the ophthalmopathy and myxedema found in hyperthyroidism [2, 5, 8]. A study of hypothyroidism found shifts in extravascular and intravascular proteins and a decrease in lymph drainage [10]. Hyperthyroidism may involve a similar pathophysiology. Given the limited information provided in the available case reports, the contribution of anticoagulation to the sanguineous nature of the pericardial effusion is unknown. For our patient, the presence of RBCs in the pericardial effusion and pleural effusion, albeit a small amount in the pleural effusion, suggested that anticoagulation may be a factor in the development of sanguineous pericardial effusions in the setting of Graves’ disease, assuming that the procedures were not notably traumatic.

In the case of pericardial effusions, the absence or presence of tamponade physiology can dictate the necessity of urgent pericardiocentesis. Our patient developed cardiac tamponade physiology and required pericardiocentesis. In several of the previously reported cases, the pericardial effusion resolved with treatment of hyperthyroidism alone [2, 3, 6].

Pericardial effusions usually undergo further diagnostic evaluation, as the etiology may be caused by malignancy or tuberculosis. In a United States study, 64% of pericardial effusions were sanguineous, and malignancy and tuberculosis caused 26% and 1%, respectively, of the sanguineous pericardial effusions [11]. Seventy percent of malignant pericardial effusions were serosanguineous or sanguineous in an Israeli population [12]. In other studies of sanguineous pericardial effusions, malignancy and tuberculosis accounted for 13–45.6% and 4–28.6%, respectively, of pericardial effusions [1316]. Our patient appeared to have neither of these etiologies, as culture and cytology of his pericardial fluid did not grow mycobacteria or reveal malignant cells. Furthermore, with treatment for his hyperthyroidism, his pericardial effusion did not recur.

We describe a case of a patient with Graves’ disease complicated by sanguineous pericardial effusion, cardiac tamponade, and atrial fibrillation. This condition is rare, with only 10 previously reported cases. Our case is similar to previously reported cases, except that we believe this is the first reported case of sanguineous pericardial effusion involving a heparin infusion. Clinicians should be mindful that although rare, pericardial effusions and cardiac tamponade can be due to hyperthyroidism and that sanguineous pericardial effusion, usually associated with malignancy or tuberculosis, can be due to Graves’ disease. Because a pericardial effusion may be sanguineous, the risk of bleeding from the use of anticoagulation for atrial fibrillation should be considered in the setting of hyperthyroidism. The American Heart Association, the American College of Cardiology, and the Heart Rhythm Society recommend administering anticoagulation in the setting of hyperthyroidism based on validated risk factors and risk scoring systems such as CHA2DS2-VASc (congestive heart failure, hypertension, age ≥75 years [doubled], diabetes mellitus, prior stroke or transient ischemic attack or thromboembolism, vascular disease, age 65 to 74 years, and sex category) [17, 18].


LDH:Lactate dehydrogenase
RBC:Red blood cell
TSH:Thyroid stimulating hormone
TTE:Transthoracic echocardiography.


The views expressed in this paper do not communicate an official position of The University of New Mexico.

Competing Interests

The authors declare that they have no competing interests.

Authors’ Contributions

All authors participated in the drafting, revision, and finalization of the paper and approved the paper for submission and publication.


Cecilia Kieu assisted in the preparation of the figures for this paper.


  1. J. G. Hollowell, N. W. Staehling, W. D. Flanders et al., “Serum TSH, T4, and thyroid antibodies in the United States population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III),” Journal of Clinical Endocrinology and Metabolism, vol. 87, no. 2, pp. 489–499, 2002. View at: Publisher Site | Google Scholar
  2. N. R. A. Clarke, A. P. Banning, D. J. Gwilt, and A. R. Scott, “Pericardial disease associated with Grave's thyrotoxicosis,” Quarterly Journal of Medicine, vol. 95, no. 3, pp. 188–189, 2002. View at: Publisher Site | Google Scholar
  3. Y. Khalid, R. Sulaiman, R. Zahir, V. Baskar, and H. N. Buch, “An unusual complication in a patient with Graves' disease,” The New Zealand Medical Journal, vol. 124, no. 1341, pp. 69–71, 2011. View at: Google Scholar
  4. P.-Y. Levy, R. Corey, P. Berger et al., “Etiologic diagnosis of 204 pericardial effusions,” Medicine, vol. 82, no. 6, pp. 385–391, 2003. View at: Publisher Site | Google Scholar
  5. A. Nakata, R. Komiya, Y. Ieki, H. Yoshizawa, S. Hirota, and E. Takazakura, “A patient with Graves' disease accompanied by bloody pericardial effusion,” Internal Medicine, vol. 44, no. 10, pp. 1064–1068, 2005. View at: Publisher Site | Google Scholar
  6. S. Ovadia, L. Lysyy, and T. Zubkov, “Pericardial effusion as an expression of thyrotoxicosis,” Texas Heart Institute Journal, vol. 34, no. 1, pp. 88–90, 2007. View at: Google Scholar
  7. E. Teague, C. J. O'Brien, and N. P. S. Campbell, “Pericardial effusion and tamponade complicating treated graves' thyrotoxocosis,” Ulster Medical Journal, vol. 78, no. 1, pp. 56–57, 2009. View at: Google Scholar
  8. M. G. Y. Yu, H. Urbanozo, and M. Fusilero, “Thyrotoxic pericardial effusion complicating graves’ disease in pregnancy,” Journal of the ASEAN Federation of Endocrine Societies, vol. 30, no. 1, pp. 44–47, 2015. View at: Publisher Site | Google Scholar
  9. U. M. Kabadi and S. P. Kumar, “Pericardial effusion in primary hypothyroidism,” American Heart Journal, vol. 120, no. 6, part 1, pp. 1393–1395, 1990. View at: Publisher Site | Google Scholar
  10. H. H. Parving, J. M. Hansen, S. L. Nielsen, N. Rossing, O. Munck, and N. A. Lassen, “Mechanisms of edema formation in myxedema—increased protein extravasation and relatively slow lymphatic drainage,” The New England Journal of Medicine, vol. 301, no. 9, pp. 460–465, 1979. View at: Publisher Site | Google Scholar
  11. S. Atar, J. Chiu, J. S. Forrester, and R. J. Siegel, “Bloody pericardial effusion in patients with cardiac tamponade. Is the cause cancerous, tuberculous, or latrogenic in the 1990s?” Chest, vol. 116, no. 6, pp. 1564–1569, 1999. View at: Publisher Site | Google Scholar
  12. S. Ben-Horin, I. Bank, A. Shinfeld, E. Kachel, V. Guetta, and A. Livneh, “Diagnostic value of the biochemical composition of pericardial effusions in patients undergoing pericardiocentesis,” American Journal of Cardiology, vol. 99, no. 9, pp. 1294–1297, 2007. View at: Publisher Site | Google Scholar
  13. B. C. Cho, S.-M. Kang, D.-H. Kim et al., “Clinical and echocardiographic characteristics of pericardial effusion in patients who underwent echocardiographically guided pericardiocentesis: Yonsei Cardiovascular Center experience, 1993–2003,” Yonsei Medical Journal, vol. 45, no. 3, pp. 462–468, 2004. View at: Publisher Site | Google Scholar
  14. C. R. Gibbs, R. D. S. Watson, S. P. Singh, and G. Y. H. Lip, “Management of pericardial effusion by drainage: a survey of 10 years' experience in a city centre general hospital serving a multiracial population,” Postgraduate Medical Journal, vol. 76, no. 902, pp. 809–813, 2000. View at: Publisher Site | Google Scholar
  15. W. Ma, J. Liu, Y. Zeng et al., “Causes of moderate to large pericardial effusion requiring pericardiocentesis in 140 Han Chinese patients,” Herz, vol. 37, no. 2, pp. 183–187, 2012. View at: Publisher Site | Google Scholar
  16. J. Sagristà-Sauleda, J. Mercé, G. Permanyer-Miralda, and J. Soler-Soler, “Clinical clues to the causes of large pericardial effusions,” American Journal of Medicine, vol. 109, no. 2, pp. 95–101, 2000. View at: Publisher Site | Google Scholar
  17. C. T. January, L. S. Wann, J. S. Alpert et al., “American College of Cardiology/American Heart Association Task Force on Practice Guidelines. 2014 AHA/ACC/HRS guideline for the management of patients with atrial fibrillation: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the Heart Rhythm Society,” Journal of the American College of Cardiology, vol. 64, no. 21, pp. e1–e76, 2014. View at: Publisher Site | Google Scholar
  18. G. Y. H. Lip, R. Nieuwlaat, R. Pisters, D. A. Lane, and H. J. G. M. Crijns, “Refining clinical risk stratification for predicting stroke and thromboembolism in atrial fibrillation using a novel risk factor-based approach: The Euro Heart Survey on atrial fibrillation,” Chest, vol. 137, no. 2, pp. 263–272, 2010. View at: Publisher Site | Google Scholar

Copyright © 2016 Peter V. Bui et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

1572 Views | 416 Downloads | 1 Citation
 PDF  Download Citation  Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

We are committed to sharing findings related to COVID-19 as quickly and safely as possible. Any author submitting a COVID-19 paper should notify us at to ensure their research is fast-tracked and made available on a preprint server as soon as possible. We will be providing unlimited waivers of publication charges for accepted articles related to COVID-19. Sign up here as a reviewer to help fast-track new submissions.