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A Case of Non-Functioning Huge Adrenocortical Carcinoma Extending Into Inferior Vena Cava and Right Atrium
Article in En | WPRIM | ID: wpr-65022
Responsible library: WPRO
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.
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Full text: 1 Index: WPRIM Main subject: Vena Cava, Inferior / Biopsy / Remission Induction / Echocardiography / Tomography, X-Ray Computed / Follow-Up Studies / Adrenal Cortex Neoplasms / Adrenocortical Carcinoma / Heart Atria / Heart Neoplasms Type of study: Observational_studies / Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: Journal of Korean Medical Science Year: 2006 Type: Article
Full text: 1 Index: WPRIM Main subject: Vena Cava, Inferior / Biopsy / Remission Induction / Echocardiography / Tomography, X-Ray Computed / Follow-Up Studies / Adrenal Cortex Neoplasms / Adrenocortical Carcinoma / Heart Atria / Heart Neoplasms Type of study: Observational_studies / Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: Journal of Korean Medical Science Year: 2006 Type: Article