Abstract
Primary adrenocortical carcinoma (ACC) is a rare tumor and its usual sites of metastasis are the lung (71%), lymph node (68%), liver (42%), and bone (26%). However, intracaval invasion extending into the right atrium is very rare and spontaneous regression of tumor burden in adrenal carcinoma is also rare. We report a case of ACC with direct invasion of the inferior vena cava and right atrium. A 34-yr-old male patient presented with progressive dyspnea, weight loss, and poor oral intake over 3 months. Non-functioning ACC with direct invasion of the inferior vena cava and right atrium was confirmed by imaging, pathologic, and hormonal study. Chemo-radiotherapy was attempted. However, tumor burden was not changed, but rather toxic hepatitis and thrombocytopenia were developed. His subjective symptoms and general conditions were improved after 1 month of conservative management and the patient was discharged. During clinical follow-up, this tumor showed spontaneous regression. Copyright © The Korean Academy of Medical Sciences.
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Kye, H. K., Jong, C. P., Sang, Y. L., Il, S. S., Kyung, H. Y., Sang, H. C., … Jung, C. K. (2006). A case of non-functioning huge adrenocortical carcinoma extending into inferior vena cava and right atrium. Journal of Korean Medical Science, 21(3), 572–576. https://doi.org/10.3346/jkms.2006.21.3.572
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