Hypertension and severe hypokalaemia associated with ectopic ACTH production

Ectopic adrenocorticotropic hormone (ACTH) secretion represents 5%–10% of cases of Cushing’s syndrome (CS), and approximately 50%–60% of these arise from neuroendocrine lung tumours, including small-cell lung cancer (SCLC). We report a 42-year-old man admitted with hypertension, metabolic alkalosis...

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Bibliographic Details
Published in:BMJ case reports Vol. 2018; p. bcr-2017-223406
Main Authors: Lobo Ferreira, Tiago, Nunes da Silva, Tiago, Canário, Dolores, Francisca Delerue, Maria
Format: Journal Article
Language:English
Published: England BMJ Publishing Group LTD 16-08-2018
BMJ Publishing Group
Series:Case Report
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Summary:Ectopic adrenocorticotropic hormone (ACTH) secretion represents 5%–10% of cases of Cushing’s syndrome (CS), and approximately 50%–60% of these arise from neuroendocrine lung tumours, including small-cell lung cancer (SCLC). We report a 42-year-old man admitted with hypertension, metabolic alkalosis and severe hypokalaemia. On physical examination, centripetal obesity with ‘moon face’ and ‘buffalo’s hump’ were identified, and wheezing on left lung was heard. A markedly elevated serum cortisol, ACTH and urine free cortisol production supported the diagnosis of CS. Chest CT showed a left hilar mass with metastasis to the liver, adrenal glands and lymph nodes. Bronchoscopy identified bronchial infiltration by SCLC. Treatment with metyrapone and chemotherapy was started. Despite initial improvement, progressive clinical deterioration occurred, culminating in death 1 year after diagnosis. Ectopic ACTH secretion is uncommon but should be suspected in patients with severe hypokalaemia, hypertension and metabolic alkalosis, especially in the context of lung cancer.
Bibliography:ObjectType-Case Study-2
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ISSN:1757-790X
1757-790X
DOI:10.1136/bcr-2017-223406