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1.
BCCR-Basic and Clinical Cancer Research. 2011; 3 (1): 30-35
in English | IMEMR | ID: emr-137512

ABSTRACT

In this study we evaluated the incidence of hypothyroidism in patients who received external beam radiation due to cancer, when radiation portals included thyroid gland. This prospective study was conducted from April 2004 to December 2005 among patients with head and neck or breast malignancies who referred to Radiation Oncology Department of Cancer Institute, Imam Khomeini hospital, treated with external beam radiotherapy. All patients received radiation to the thyroid gland. Thyroid function was tested at the beginning of treatment, 3 months and 6 months after the completion of radiotherapy. In all 34 patients were included in the study. The median age of patients was 53 years. Eighteen patients were female and 16 were male. All patients received external radiotherapy. They received radiation ranging from 5000 cGY [14 patients 41.2%] to 7400 cGY [1 patient 2.9%] with median of 6000 cGY. Physical examination of thyroid at the beginning of treatment was normal and all of the patients were euthyroid. The results from TSH test showed significant difference at baseline, after 3 and 6 months follow-up [P =0.001]. The findings indicated that none of the patients developed hypothyroidism in a period of six months after completion of radiotherapy. However, it seems that 6 months fallow-up is early for judgment about evaluation of patients for hypothyroidism state and it needs further follow up for minimum of 12 months


Subject(s)
Humans , Radiotherapy/adverse effects , Head and Neck Neoplasms/radiotherapy , Prospective Studies , Radiation Oncology , Evaluation Studies as Topic , Hypothyroidism/etiology , Thyroid Function Tests
2.
International Journal of Radiation Research. 2005; 2 (4): 215-218
in English | IMEMR | ID: emr-176799

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, 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

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