Giant adrenocortical carcinoma simulating a liver tumor

A. B. Miled, C. Dziri, H. Jerraya, I. Bouasker, Mohamed Ali, R. Nouira, W. Dougaz
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Abstract

Adrenocortical carcinoma is a rare malignant tumor which can reach large sizes if it is nonfunctioning. In that situation, it can pose diagnosis dilemmas regarding the origin and the nature of the tumor. We reported a case of non-secreting and large right Adrenocortical carcinoma which arose in the posterior costophrenic angle mimicking a liver tumor. A 45-year-old man presented with a voluminous abdominal mass in the right upper quadrant. The different imaging modalities including ultrasound computed tomography and magnetic resonance imaging were discordant as regards the hepatic or the adrenal origin of the tumor. Percutaneous biopsy allowed to determine the diagnosis of the cortico-adrenal tumor. The patient underwent laparotomy. The tumor which arose from the right adrenal gland was resected. Pathology confirmed the diagnosis of adrenocortical carcinoma with histological factors of poor prognosis. The patient was given Mitotane as adjuvant therapy. After six years of follow-up, a tumor recurrence has been diagnosed.
巨大肾上腺皮质癌模拟肝脏肿瘤
肾上腺皮质癌是一种罕见的恶性肿瘤,如果没有功能,可达到很大的体积。在这种情况下,它可能会对肿瘤的起源和性质造成诊断困境。我们报告一例非分泌性大右肾上腺皮质癌,发生于肋膈角后部,形似肝肿瘤。45岁男性,右上腹部有巨大肿块。不同的成像方式,包括超声计算机断层扫描和磁共振成像是不一致的关于肝脏或肾上腺肿瘤的起源。经皮活检可以确定肾上腺皮质肿瘤的诊断。病人接受了剖腹手术。右肾上腺肿瘤被切除。病理证实为肾上腺皮质癌,组织学因素预后不良。患者给予米托坦辅助治疗。经过六年的随访,诊断出肿瘤复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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