Department of Diabetes and Endocrinology, Mater Dei Hospital, Msida, Malta
Department of Diabetes and Endocrinology, Mater Dei Hospital, Msida, Malta.
BMJ Case Rep. 2021 May 6;14(5):e240290. doi: 10.1136/bcr-2020-240290.
An elderly gentleman was admitted to hospital with severe hypokalaemia of 1.75mmol/L. A background of a recently diagnosed metastatic gastric carcinoma with a neuroendocrine component pointed towards the diagnosis of ectopic ACTH secretion causing this dangerous electrolyte imbalance. He was treated with aggressive potassium supplementation and the adrenal steroid synthesis blocker metyrapone to acutely control his Cushing's syndrome. Chemotherapy consisting of carboplatin/etoposide combination was initiated but unfortunately the patients' health deteriorated, and he died three months after his initial diagnosis. This case highlights the accelerated presentation of hypercortisolism due to ectopic ACTH secretion. It discusses the classification of neuroendocrine tumours and their varied prognosis depending on the underlying tumour grade. It emphasises the importance of having a multidisciplinary team to be able to care for two underlying pathologies simultaneously: both the severe hypercortisolism and his metastatic gastric tumour.
一位老年绅士因严重低钾血症(1.75mmol/L)入院。最近诊断出患有转移性胃神经内分泌癌,这表明可能是异位 ACTH 分泌导致这种危险的电解质失衡。他接受了积极的钾补充和肾上腺类固醇合成抑制剂甲吡酮治疗,以急性控制库欣综合征。开始使用卡铂/依托泊苷联合化疗,但不幸的是,患者病情恶化,在最初诊断后的三个月去世。本病例强调了由于异位 ACTH 分泌导致皮质醇增多症加速表现。讨论了神经内分泌肿瘤的分类及其不同的预后,取决于潜在肿瘤分级。它强调了拥有多学科团队的重要性,以便能够同时治疗两种潜在的疾病:严重的皮质醇增多症和转移性胃肿瘤。