Soundarrajan Malini, Zelada Henry, Fischer Jean Victoria, Kopp Peter
AACE Clin Case Rep. 2019 Apr 25;5(3):e192-e196. doi: 10.4158/ACCR-2018-0429. eCollection 2019 May-Jun.
Neuroendocrine differentiation of prostate cancer can result in ectopic adrenocorticotropic hormone (ACTH) secretion (EAS) and Cushing syndrome. The aim of this report is to highlight this unusual mechanism of hypercortisolism and its management.
We report a 73-year-old patient with a history of prostate adenocarcinoma who presented with severe weakness, hyperglycemia, and hypokalemia caused by EAS.
Diagnostic workup showed elevated 24-hour urine cortisol and ACTH levels consistent with EAS. Fluorodeoxyglucose positron emission tomography-computed tomography revealed a hypermetabolic mass in the prostate and metastatic lesions to the liver and bones. Liver biopsy was consistent with small cell carcinoma with positive immunostaining for ACTH. Pleural fluid analysis was consistent with high-grade neuroendocrine carcinoma. The patient underwent chemotherapy with carboplatin and etoposide. Hypercortisolism was treated with ketoconazole, metyrapone, mifepristone, and spironolactone. He suffered complications including opportunistic infections, deep venous thrombosis, and delirium. Given his poor prognosis and clinical decline, the patient opted for comfort measures only in a hospice facility.
Treatment-related neuroendocrine differentiation of prostate cancer is an emerging entity that may be associated with paraneoplastic syndromes including EAS.
前列腺癌的神经内分泌分化可导致异位促肾上腺皮质激素(ACTH)分泌(EAS)和库欣综合征。本报告的目的是强调这种不寻常的皮质醇增多症机制及其管理。
我们报告一名73岁有前列腺腺癌病史的患者,因EAS出现严重虚弱、高血糖和低钾血症。
诊断检查显示24小时尿皮质醇和ACTH水平升高,与EAS一致。氟脱氧葡萄糖正电子发射断层扫描-计算机断层扫描显示前列腺有高代谢肿块以及肝脏和骨骼的转移病灶。肝活检符合小细胞癌,ACTH免疫染色呈阳性。胸腔积液分析符合高级别神经内分泌癌。该患者接受了卡铂和依托泊苷化疗。皮质醇增多症用酮康唑、美替拉酮、米非司酮和螺内酯治疗。他出现了包括机会性感染、深静脉血栓形成和谵妄在内的并发症。鉴于其预后不良和临床状况恶化,患者选择仅在临终关怀机构接受姑息治疗。
前列腺癌与治疗相关的神经内分泌分化是一种新出现的情况,可能与包括EAS在内的副肿瘤综合征有关。