| Literature DB >> 27170604 |
Sara Maki1, Caroline Kramarz1, Paula Maria Heister2, Kamran Pasha3.
Abstract
Addison's disease is a rare endocrine disorder that frequently presents with non-specific symptoms, but may deteriorate rapidly into life-threatening Addisonian crisis if left untreated. Diagnosis can be difficult in patients without a suggestive medical history. We describe a case of a 37-year-old man who was admitted with acute kidney injury and hyperkalaemia, resistant to treatment with insulin/dextrose and calcium gluconate. On clinical examination, he was found to be hyperpigmented; a subsequent random serum cortisol of 49 nmol/L affirmed the preliminary diagnosis of Addison's disease. The patient's hyperkalaemia improved on treatment with hydrocortisone, and a follow-up morning adrenocorticotropic hormone of 1051 ng/L confirmed the diagnosis. 2016 BMJ Publishing Group Ltd.Entities:
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Year: 2016 PMID: 27170604 PMCID: PMC4885262 DOI: 10.1136/bcr-2015-213375
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X