| Literature DB >> 30661045 |
Marius Vögelin1, Richard Cathomas2, Niklaus Kamber3, Thomas Fehr1.
Abstract
Two years after diagnosis of a metastatic neuroendocrine gastrin-secreting tumour and after several cycles of chemotherapy and peptide receptor radionuclide therapy, a 56-year-old woman presented with hypokalaemic metabolic alkalosis, hypertension, leg oedema and new-onset diabetes mellitus. Further investigations revealed renal potassium loss confirmed by a transtubular potassium gradient of 16, fully suppressed serum aldosterone, but instead highly elevated blood levels of morning cortisol and adrenocorticotropic hormone as well as increased urinary excretion of glucocorticoid and mineralocorticoid metabolites. Ruling out other causes, paraneoplastic hypercortisolism was diagnosed. Pharmacological inhibition of the steroid 11β-hydroxylase with metyrapone resulted in complete resolution of metabolic alkalosis, hypokalaemia, hypertension, hyperglycaemia and leg oedema within 1 week. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: diabetes; drugs: endocrine system; endocrine cancer; fluid electrolyte and acid-base disturbances; hypertension
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Year: 2019 PMID: 30661045 PMCID: PMC6340553 DOI: 10.1136/bcr-2018-227068
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X