Department of Endocrine and Breast Surgery, Madras Medical College and Research Institute, Chennai, Tamil Nadu, India
Department of Endocrine and Breast Surgery, Madras Medical College and Research Institute, Chennai, Tamil Nadu, India.
BMJ Case Rep. 2020 Sep 9;13(9):e235317. doi: 10.1136/bcr-2020-235317.
Adrenocortical carcinomas (ACCs) are rare malignancies with an incidence of one to two per million per year. Aldosterone-producing ACCs (APACs) are extremely rare with an incidence less than 1%. We describe a rare case of APAC, presenting with episodic lower-limb weakness and hypertension. Our patient was found to have serum aldosterone levels of 20.8 ng/dL (2.5-15.2) with persistent hypokalaemia and a 9.7×8.3×7.7 cm right adrenal mass, which was suspicious of malignancy on evaluation. He underwent a complete surgical resection which confirmed the diagnosis of ACC and normalised his aldosterone and potassium levels. He was then subjected to postoperative chemotherapy. Postoperative adjuvant chemotherapy with mitotane has a role in preventing recurrence.
肾上腺皮质癌(ACC)是一种罕见的恶性肿瘤,发病率为每年每百万分之一至二。产生醛固酮的 ACC(APAC)极为罕见,发病率低于 1%。我们描述了一例罕见的 APAC 病例,表现为间歇性下肢无力和高血压。我们的患者血清醛固酮水平为 20.8ng/dL(2.5-15.2),持续低钾血症和 9.7×8.3×7.7cm 右侧肾上腺肿块,评估后怀疑为恶性肿瘤。他接受了完整的手术切除,确诊为 ACC,并使他的醛固酮和钾水平恢复正常。然后他接受了术后化疗。术后辅助化疗 mitotane 可预防复发。