Lenh Bui-Van, Duc Nguyen Minh, Tra My Thieu-Thi, Minh Tran Ngoc, Bang Luong Viet, Linh Le Tuan, Giang Bui-Van, Thong Pham Minh
Department of Radiology, Hanoi University Medical Hospital, Hanoi, Vietnam.
Department of Radiology, Hanoi Medical University, Hanoi, Vietnam.
Radiol Case Rep. 2021 Apr 3;16(6):1329-1334. doi: 10.1016/j.radcr.2021.03.006. eCollection 2021 Jun.
Adrenocortical carcinoma (ACC) is a rare malignancy that arises from the adrenal cortex and can be classified as either non-functioning or functioning. A patient with non-functioning ACC may present no specific symptoms. Imaging analysis can provide some information to a clinician who suspects ACC, such as tumor size, density, washout, necrosis, hemorrhage, and calcification. Histopathology is used to confirm and determine the origin of the malignancy and can provide relevant prognostic information. Microscopic findings can be used to obtain information such as the Weiss score, resection surface features, Ki-67 proliferative index, and the degree of capsular and vascular invasion. Surgery can be curative for localized tumors, and adjuvant therapy using mitotane and cytotoxic chemotherapy is often employed for advanced-stage tumors. We describe a case report of a 32-year-old man with a non-functioning ACC that highlights the importance of radiological and pathological features in the diagnosis of ACC and their use as prognostic factors.
肾上腺皮质癌(ACC)是一种起源于肾上腺皮质的罕见恶性肿瘤,可分为无功能性或功能性。无功能性ACC患者可能没有特定症状。影像学分析可为怀疑患有ACC的临床医生提供一些信息,如肿瘤大小、密度、廓清、坏死、出血和钙化情况。组织病理学用于确诊并确定恶性肿瘤的起源,还可提供相关的预后信息。微观检查结果可用于获取诸如Weiss评分、切除表面特征、Ki-67增殖指数以及包膜和血管侵犯程度等信息。手术对于局限性肿瘤可能具有治愈效果,而对于晚期肿瘤通常采用米托坦和细胞毒性化疗进行辅助治疗。我们描述了一例32岁无功能性ACC男性患者的病例报告,该报告强调了放射学和病理学特征在ACC诊断中的重要性及其作为预后因素的应用。