Primary cardiac sarcoma A case report

Authors

  • Paulo Ferreira Interno do Internato Complementar de Medicina Interna dos HUC
  • Nascimento Costa Chefe de Serviço de Medicina Interna dos HUC; Professor Agregado da FMC
  • Anabela Sá Assistente Hospitalar de Medicina Interna dos HUC
  • Adriano Rodrigues Assistente Graduado de Medicina Interna dos HUC; Professor Associado da FMC
  • Armando Porto Director do Serviço de Medicina III dos HUC; Professor Catedrático da FMC

Keywords:

Primary cardiac sarcoma, echo-cardiography, surgery, chemotherapy

Abstract

Primary cardiac sarcomas are rare entities, with non-specific clinical presentations. Transthoracic echocardiography
is the most efficient method for diagnosis, but for certain
sites, transoesophageal echocardiography is more sensitive. Surgery is the therapy of choice, whereas the role of
adjuvant treatment is contraversial.
The authors present a case report of a malignant fibrous
histiocytoma in a 63-year-old female patient who underwent
surgery and adjuvant chemotherapy has survived for 3 years
to date. The diagnostic strategy and therapeutic options are
discussed as well as the excxellent results obtained in the clinical case described. 

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References

Reynen K. Frequency of primary tumors of the heart. Am J Cardiol 1996; 77 (1): 107-109.

Burke A, Virmani R. Tumors of the heart and great vessels. Primary cardiac sarcomas. In: Atlas of tumor pathology. 3rd series. Fascicle 16.

Washington: Armed Forces Institute of Pathology 1996; 127-170.

Poole GV, Meredith JW, Breyer RH, Mills SA. Surgical implications in malignant cardiac disease. Ann Thorac Surg 1983; 36 (4): 484-491.

Burke AP, Cowan D, Virmani R. Primary sarcomas of the heart. Cancer 1992; 69 (2): 387-395.

Llombart-Cussac A, Pivot X, Contesso G et al. Adjuvant chemotherapy for primary cardiac sarcomas: the IGR experience. Br J Cancer 1998;

(12): 1624-1628.

Movsas B, Teruya-Feldstin J, Smith J, Glatstein E, Epstein AH. Primary cardiac sarcoma. A novel treatment approach. Chest 1998; 114: 648-652.

Blanco VMR, Alvarez VB, Rojo VP, Bustinza IM, Martinez IM, Martinez EC, Llosa AC. Tumores cardíacos primários: Revisión de 29 casos. Rev

Port Cardiol 1997; 16 (12): 985-989.

Ceresoli G, Passoni P, Benussi S, Alfieri O, Dell’Antonio G, Bolognesi A. Primary cardiac sarcoma in pregnancy: a case report and review of

the literature. Am J Clin Oncol 1999; 22 (5): 460-465.

Mugge A, Daniel WG, Haverich A, Lichtlen PR. Diagnosis of noninfective cardiac mass lesions by two-dimensional echocardiography.

Comparison of the transthoracic and transesophageal approaches. Circulation 1991; 83: 70-78.

Eltabbakh GH, Belinson JL, Kennedy AW, Gupta M, Webster K, Blumenson LE. Serum CA-125 measurements > 65 U/mL. Clinical

value. J Reprod Med 1997; 42 (10): 617-624.

Seo T, Ikeda Y, Onaka H et al. Usefulness of serum CA125 measurement for monitoring pericardial effusion. Jpn Circ J 1993; 57 (6):

-494.

Centofanti P, Di Rosa E, Deorsola L et al. Primary cardiac tumors: early and late results of surgical treatment in 91 patients. Ann Thorac

Surg 1999; 68: 1236-1241.

Krüger I, Borowski A, Horst M et al. Symptoms, diagnosis and therapy of primary sarcomas of the pulmonary artery. Thorac Cardiovasc Surg 1990; 38 (2): 91-95.

Nakamichi T, Fukuda T, Suzuki T et al. Primary cardiac angiosarcoma: 53 months’ survival after multidisciplinary therapy. Ann Thorac Surg

; 63: 1160-1161

Additional Files

Published

2002-03-29

How to Cite

1.
Ferreira P, Costa N, Sá A, Rodrigues A, Porto A. Primary cardiac sarcoma A case report. RPMI [Internet]. 2002 Mar. 29 [cited 2024 May 20];9(1):32-5. Available from: https://revista.spmi.pt/index.php/rpmi/article/view/1845

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Case Reports

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