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CASE REPORT
Year : 2009  |  Volume : 10  |  Issue : 3  |  Page : 132-135 Table of Contents     

Unusual presentation of a rare tumor: Cardiac epithelioid hemangioepithelioma presenting as cardiac tamponade


1 M.D,Cardiology and Cardiothoracic Surgery Department, Hamad Medical Corporation, Doha, Qatar
2 M.D,Department of Pathology, Hamad Medical Corporation, Doha, Qatar

Date of Web Publication17-Jun-2010

Correspondence Address:
M Kahlout
M.D,Cardiology and Cardiothoracic Surgery Department, Hamad Medical Corporation, Doha
Qatar
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Source of Support: None, Conflict of Interest: None


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How to cite this article:
Kahlout M, Al-Mulla A, Chaikhouni A, Al-Bozom I. Unusual presentation of a rare tumor: Cardiac epithelioid hemangioepithelioma presenting as cardiac tamponade. Heart Views 2009;10:132-5

How to cite this URL:
Kahlout M, Al-Mulla A, Chaikhouni A, Al-Bozom I. Unusual presentation of a rare tumor: Cardiac epithelioid hemangioepithelioma presenting as cardiac tamponade. Heart Views [serial online] 2009 [cited 2021 Sep 25];10:132-5. Available from: https://www.heartviews.org/text.asp?2009/10/3/132/63710


   Introduction Top


Hemangioendothelioma is a tumor that rarely involves the heart. We present the case of a 44-year-old woman who developed cardiac tamponade due to spontaneous bleeding from cardiac hemangioendothelioma. This may be the first case report of such a complication of this rare tumor.


   Case presentation Top
A 44-year-old female patient was admitted to our hospital because of recurrent chest pain. The pain was intermittent and progressive in severity on the right side, associated with palpitation, orthopnea and paroxysmal nocturnal dyspnea. She also had productive cough, with blood-tinged sputum.

The patient gave a history of weight loss (about 8kg in 2 weeks). Six months previously, the patient was admitted because of shortness of breath due to large pericardial effusion and she was treated by echo-guided pericardiocentesis, draining about 800 ml of thin bloody fluid. The patient was discharged in stable condition and remained well until her current admission.

Transthoracic echocardiography revealed a large localized anterior pericardial effusion measuring 3.4 x 8.0cm. CT scan of the chest showed right pericardial mass, measuring 7.0 x 9.0cm, arising from the right atrium with active extravasations of the contrast from the right atrium into the pericardial cavity [Figure 1]. Multiple pulmonary nodules were present and were diagnosed as possible small multiple pulmonary emboli. MRI showed pericardial blood-filled collection measuring 5.0 x 10.0 x 6.0cm, communicating with the right atrium through a 2cm defect at the appendage with clot formation in the pseudo-aneurismal mass. The other cardiac chambers were normal; the pulmonary nodules were highly suggestive of multiple pulmonary emboli.

While being worked-up during her current hospitalization, she suddenly developed increased tachypnea and hypotension. Rupture of the pseudo-aneurysm and cardiac tamponade was suspected and an emergency operation was performed. A large pseudo-aneurysm was found in the pericardium attached to the right atrium. The right atrial wall was friable and had to be reconstructed with autogenous pericardium.

Histological examination of the resected tissue revealed a vascular tumor characterized by solid nests and cords of atypical spindled endothelial cells, some of which have distinct intracellular lumina with moderate atypia and mitotic figures [Figure 2]a. The mass was a mesenchymal tumor which stained positively for vascular markers CD31, CD34, and factor VIII confirming the diagnosis of hemangioendothelioma [Figure 2]b. Bone scan and CT scan of the head, abdomen and pelvic did not show any metastasis. The patient did well and was discharge home 12 days postoperatively.

However, 25 days later she started to complain again of chest pain, productive cough and increasing dyspnea. She was re-admitted, and CT scan of the chest showed a large antero-lateral pericardial mass measuring 8.2 x 3.7 x 6.8 cm, attached to the right atrium with signs of leaking communication between the right atrium and the mass. Transesophageal echocardiogram confirmed the same findings. The patient underwent urgent re-exploration. A similar mass with a false aneurismal cavity formation was found. The mass was more completely excised and the right atrial wall defect was repaired with autogenous pericardium.

The patient was discharged home 4 days after the operation. She received 2 courses of radiation therapy with mild improvement in the size of the residual mass. Three courses of chemotherapy were also given but she did not respond. She deteriorated progressively and eventually expired, eight months after diagnosis.


   Discussion Top


Primary tumors of the heart are rare, representing less than 5% of all cardiac tumors, with an incidence between 0.0017 and 0.19 percent in unselected patients at autopsy [1],[2],[3] . Three quarters of the tumors are benign. Myxomas comprise nearly half of the benign heart tumors and the majority of the rest are lipomas, papillary fibroelastomas, and rhabdomyomas. Whereas rhabdomyomas are the most common primary tumors of the heart in children, myxomas clearly predominate in adults [1].

Epithelioid hemangioendothelioma (EHE) is in the middle of the spectrum where epithelioid hemangioma and epithelioid angiosarcoma represent the benign and malignant variants, respectively. EHE was initially considered a low grade vascular neoplasm, but the occurrence of systemic metastases in 21%, and the fact that 17% of 20 patients died of the tumor led to the conclusion that EHE should be regarded as fully malignant, rather than a borderline, vascular neoplasm [4].

EHE is a rare vascular tumor, more commonly found in the liver, less commonly in the intestine, and very rarely in the heart. The tumor is histologically characterized by capillary-size vessels lined up by proliferating, often multilayered, epithelial-like endothelial cells with cytoplasmic vacuoles. Clinically, primary cardiac EHE may be found incidentally or after causing congestive heart failure, pericardial effusion, outflow tract obstruction, or thromboembolic event [5],[6],[7] .

EHE is classified as an intermediate malignancy that sometimes metastasizes and may recur [5],[6],[7] . Allaire [8] reported that radiation or chemotherapy resulted in palliation, whereas Hongquan [9] reported that the prognosis of EHE was relatively good if it was completely resected. Due to the malignant potential of EHE, radical resection is recommended to prevent metastasis [2],[4],[5],[6],[7],[8],[9] . However, prognosis after surgical resection is usually good.

MEDLINE search identified only 9 cases of primary cardiac EHE reported in the English literature [Table 1]. We did not find any previously published report of a patient with primary cardiac EHE presenting with spontaneous rupture and cardiac tamponade prior to this case report.


   Conclusion Top


Primary EHE is a vascular tumor that rarely involves the heart. Only nine such case reports were identified in the English literature. Echocardiography, CT scan and MRI are very helpful in making the diagnosis, but it can only be confirmed histologically. It acts as a low-grade malignant tumor, but the prognosis is usually good after surgical resection.[17]

 
   References Top

1.K. Reynen, Cardiac myxomas. N Engl J Med. 1995;33:1610-1617.  Back to cited text no. 1      
2.Reynan K., Frequency of primary tumors of the heart. Am J Cardiol. 1996;77:107-109.  Back to cited text no. 2      
3.Premkumar V. Multisided cardiac hemangiomas mimicking biatrial thrombus: atypically located cardiac hemangiomas of left atrial appendage and right atrium. J Am Soc Echocardiogr. 2006;19:107.e1-107.e2.  Back to cited text no. 3      
4.Fletcher, Christopher DM. Diagnostic Histopathology of Tumors. Philadelphia, Pennsylvania: Elsevier Science. 2000.  Back to cited text no. 4      
5.Hideki Kitamura, Hitoshi Okabayashi, Michiya Hanyu, Yoshiharu Soga, TakuyaNomoto, Hiroyuki Johno, Jota Nakano, Takehiko Matsuo, Tadaaki Yokota and, Katsumi Inoue. Successful enucleation of a giant cardiac hemangioendothelioma showing an unusual proliferation pattern. J Thorac Cardiovasc Surg 2005;130:1199-1201.   Back to cited text no. 5      
6.Gegenbach S, Ridker P. Left ventricular hemangioma in Kasbach-Merritt syndrome. Am Heart. 1991;121:202-203.   Back to cited text no. 6      
7.Marchiano D, Fisher F, Hofstetter S. Epithelioid hemangioendothelioma of the heart with distant metastases. J Cardiovascular Surgery. 1993; 34:529-533.  Back to cited text no. 7      
8.Allaire FJ, Grimm CA, Taylor LM, et al. Primary Hemangioendothelioma of the heart. Report of a case treated with irradiation and cyclophosphamide. Rocky Mt Med J. 1964;61:34-37.  Back to cited text no. 8      
9.Hongquan Y, Hua R. Cardiac hemangioendothlioma. J Cardiovasc Surg 1998;39: 655-658.  Back to cited text no. 9      
10.Ilbawi M, Deleon S, Riggs T. Primary vascular tumor of the heart in infants. Chest 1982; 81:511-512.  Back to cited text no. 10      
11.Montes Orbe PM ,Camacho I, Saracibar N, Labayen F, Ubago JL, Gallo J et al. A primary epitheliod Hemonaioendothelioma localized in the pulmonary valve. Rev Esp Cardiol 1991; 44:421-423.  Back to cited text no. 11      
12.Bille TF, Padovani R, Rosario R. Hemangioendothiluoma of the Aortic valve revealed by transient ischemic episodes. Preasse Med 1993;(38):1928-1929.   Back to cited text no. 12      
13.Mylies TD, Strassner HT, Wang DJ. Pregnancy after treatment of epitheliod hemangioendothiluoma. J Report Med 1994;39:524-526.  Back to cited text no. 13      
14.Agaimy A, Kaiser A, Wuensch PH. Epithlioudes hemangioendotheliom Association with myelodysplasstic syndrome. Z Cardiol. 2002; (91):352-356.  Back to cited text no. 14      
15.Tansel T, Aydogan O, Yilmazbayhan D, et al. Epithelioid hemangioendothelioma of the heart in infants. Ann Thoracic Surgery 2005; 79:1402-1405.   Back to cited text no. 15      
16.Vall Bernle JF, Garcia -Alberdi ,Gutierrz JA, Gariijo MF. Incidental in vivo detection of an epitheliod heamangioendothelioma of the mitral valve. Pathology International 2005;55:644-648.  Back to cited text no. 16      
17.Safirstein J, Aksenoy S, Smith F. Cardiac epithelioid hemangioendothelioma with 8-year follow-up. J foot and ankle surgery 2007;16,183-186.  Back to cited text no. 17      


    Figures

  [Figure 1], [Figure 2]
 
 
    Tables

  [Table 1]



 

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    Case presentation
    Discussion
    Conclusion
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