C. Erem, M. Kocak, H. O. Ersoz, I. Nuhoglu, S. Ersoz
{"title":"Hypertension, Diabetes, Hypokalemia, and Metabolic Alkalosis: Cushing Syndrome Secondary to Ectopic Adrenocorticotropic Hormone Secretion From Prostate Adenocarcinoma","authors":"C. Erem, M. Kocak, H. O. Ersoz, I. Nuhoglu, S. Ersoz","doi":"10.1097/TEN.0B013E3181F47CD3","DOIUrl":null,"url":null,"abstract":"Abstract: Prostate adenocarcinoma is a very rare cause of ectopic adrenocorticotropic hormone (ACTH) syndrome. We report the case of a 70-year-old man who presented with clinical and biochemical features of ACTH-dependent Cushing syndrome secondary to prostate carcinoma. On admission, his blood pressure was 170/100 mm Hg. Physical examination revealed signs of excessive production of cortisol. Laboratory values were consistent with hypokalemia and metabolic alkalosis. Elevated serum cortisol, ACTH, and urine free cortisol levels were found. Cortisol was not suppressed with an overnight 1-mg oral dexamethasone suppression test (DST), 2-day low-dose DST, or overnight 8.0-mg high-dose DST. Chest computed tomography showed multiple parenchymal nodules in the right lung, consistent with metastatic disease. Whole-body bone scintigraphy revealed numerous foci of increased radiotracer uptake in the femur and axial skeleton, consistent with metastatic disease. Bone survey (radiography) showed generalized osteolytic metastases. Histologic analysis of a prostatic biopsy showed prostate adenocarcinoma. Immunostaining of the prostate adenocarcinoma for ACTH was positive. The severe metabolic alkalosis due to glucocorticoid-induced mineralocorticoid excess was treated with potassium supplements and spironolactone. This case is a remarkable example of the complex metabolic endocrine manifestations that can accompany prostate adenocarcinoma.","PeriodicalId":50531,"journal":{"name":"Endocrinologist","volume":"52 1","pages":"211-213"},"PeriodicalIF":0.0000,"publicationDate":"2010-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Endocrinologist","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/TEN.0B013E3181F47CD3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Abstract: Prostate adenocarcinoma is a very rare cause of ectopic adrenocorticotropic hormone (ACTH) syndrome. We report the case of a 70-year-old man who presented with clinical and biochemical features of ACTH-dependent Cushing syndrome secondary to prostate carcinoma. On admission, his blood pressure was 170/100 mm Hg. Physical examination revealed signs of excessive production of cortisol. Laboratory values were consistent with hypokalemia and metabolic alkalosis. Elevated serum cortisol, ACTH, and urine free cortisol levels were found. Cortisol was not suppressed with an overnight 1-mg oral dexamethasone suppression test (DST), 2-day low-dose DST, or overnight 8.0-mg high-dose DST. Chest computed tomography showed multiple parenchymal nodules in the right lung, consistent with metastatic disease. Whole-body bone scintigraphy revealed numerous foci of increased radiotracer uptake in the femur and axial skeleton, consistent with metastatic disease. Bone survey (radiography) showed generalized osteolytic metastases. Histologic analysis of a prostatic biopsy showed prostate adenocarcinoma. Immunostaining of the prostate adenocarcinoma for ACTH was positive. The severe metabolic alkalosis due to glucocorticoid-induced mineralocorticoid excess was treated with potassium supplements and spironolactone. This case is a remarkable example of the complex metabolic endocrine manifestations that can accompany prostate adenocarcinoma.
摘要:前列腺腺癌是异位促肾上腺皮质激素(ACTH)综合征的罕见病因。我们报告的情况下,70岁的男子谁提出的acth依赖性库欣综合征继发于前列腺癌的临床和生化特征。入院时血压为170/100 mm Hg,体格检查显示皮质醇分泌过多。实验室值符合低钾血症和代谢性碱中毒。血清皮质醇、ACTH和尿游离皮质醇水平升高。1 mg口服地塞米松抑制试验(DST)、2天低剂量DST或8 mg高剂量DST均未抑制皮质醇。胸部计算机断层扫描显示右肺多发实质结节,符合转移性疾病。全身骨显像显示股骨和中轴骨骼中大量放射性示踪剂摄取增加的病灶,与转移性疾病一致。骨检查(x线摄影)显示广泛性溶骨转移。前列腺活检的组织学分析显示前列腺腺癌。前列腺腺癌ACTH免疫染色阳性。糖皮质激素引起的矿皮质激素过量引起的严重代谢性碱中毒用钾补充剂和螺内酯治疗。本病例是前列腺腺癌伴发复杂代谢内分泌表现的典型例子。