An unusual case of profound hyponatraemia and bilateral adrenal calcifications

Charmaine Cassar, Richard Procter, Fraser Davidson, Andrew Collier, Iqbal A. Malik, Sujoy Ghosh, Tarik A. Elhadd

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

We report a case of a 65-year-old lady who presented with acute confusion and profound hyponatraemia (plasma sodium of 97 mmol/L). Five years earlier she had developed sepsis and was found to have hyponatraemia, thought to be due to syndrome of inappropriate antidiuretic hormone secretion. The patient was lost to follow-up. The patient was covered with steroids and investigations confirmed primary adrenal failure with flat response of cortisol to adrenocorticotropic hormone (ACTH) stimulation and very high level of ACTH. Adrenal auto-antibodies were negative and a computed tomography of the adrenals showed bilateral adrenal calcifications, suggestive of previous haemorrhage or infarction. Bilateral adrenal calcification due to haemorrhage/infarction usually does not present with severe hyponatraemia; however, adrenal insufficiency should be excluded in all cases of severe hyponatraemia. In suspected cases, patients should be treated with steroids, even when symptoms or signs are absent, while results of investigations are awaited.
Original languageEnglish
Pages (from-to)523-526
Number of pages4
JournalAnnals of Clinical Biochemistry
Volume46
Issue number6
Early online date1 Oct 2009
DOIs
Publication statusPublished - Nov 2009
Externally publishedYes

ASJC Scopus subject areas

  • Clinical Biochemistry

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