A 72-year-old male diagnosed with heart failure and dyspnea was found to have a lesion in his right atrium. Histological examination of the tumor revealed it to be a malignant fibrous histiocytoma. The patient's management and subsequent follow-up are presented.
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References
1.
StevensCWSears-RoganPBittermanPTorrisiJ. Treatment of malignant fibrous histiocytoma of the heart. Cancer1992; 69: 956–961.
2.
GaffneyEFDervanPAFletcherCD. Pleomorphic rhabdomyosarcoma in adulthood. Analysis of 11 cases with definition of diagnostic criteria. Am J Surg Pathol1993;17:601–9.
3.
BurkeAPCowanDVirmaniR. Primary sarcomas of the heart. Cancer1992;69:378–95.
4.
WeissSWGoldblumJR. Malignant fibrohistiocytic tumors. In: Enzinger and Weiss's Soft tissue tumors4th edition. St. Louis, Mosby2001:535–69.
5.
HsiehPLLeeDChiouKRKungMHLinSLLiuCP. Echocardiographic features of primary cardiac sarcoma. Echocardiography2002;19:215–20.
6.
Vander SalmTJ. Unusual primary tumors of the heart. Semin Thorac Cardiovasc Surg2000;12:89–100.
7.
KamiyaHYasudaTNagamineHSakakibaraNNishidaSKawasujiM. Surgical treatment of primary cardiac tumors: 28 years’ experience in Kanazawa University Hospital. Jpn Circ J2001;65:315–9.
8.
SchenaSCanigliaAAgninoACarusoGFerlanG. Survival following treatment of a cardiac malignant fibrous histiocytoma. Chest2000;118:271–3.