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Iranian Journal of Radiation Research
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:: Volume 2, Number 4 (3-2005) ::
Back to browse issues page Volume 2, Number 4 ( 3-2005), Pages 215 - 218
XML Cardiac angiosarcoma; Report of a case Print

Author(s): M. Sardari Kermani *, F. Razi and E. Esmati
Department of Radiation Oncology, Cancer Institute, Tehran University of Medical Sciences, Tehran, Iran Sardarik@sina.tums.ac.ir
Study Type: Reviews and Perspectives | Subject: Radiation Biology
Article abstract:

ABSTRACT

Sarcomas are the most malignant tumors in the myocardium. Most common sarcoma is the

angiosarcoma, classically located in the right atrium. Surgical resection is the primary treatment

of choice for these patients. In July 2003, an 18 years old man with chest pain and dyspnea,

referred to the Imam Khomeini Hospital. Chest X-ray showed cardiac enlargement and

transthoracic echocardiography demonstrated a large lobulated tumoral mass in right atrium.

Cytologic examination of the pericardial effusion reported as no evidence of malignancy and

chest CT scan showed cardiac dilatation with blood density and pericardial effusion. The patient

underwent operation and tumor bulk was resected. Based on histological examination and

immunohistochemistry, diagnosis of cardiac angiosarcoma was made and the patient received

postoperative radiotherapy through parallel-opposed AP-PA cobalt beam technique. After

combined modality treatment with surgery and postoperative radiotherapy, symptoms were

disappeared and after 20 month follow up patient is symptom free. Despite of the ominous

outcome of this malignancy an multimodality approach is worthy of consideration.

Radiat. Res., 2005; 2 (4): 215-218

Iran. J.
Keywordsimmunohistochemistry, adjuvant radiotherapy, Cardiac angiosarcoma,

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Back to browse issues page Volume 2, Number 4 ( 3-2005), Pages 215 - 218
Iranian Journal of Radiation Research
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