Two Cases of Isolated ACTH Deficiency Presenting As Hyponatremia - Case Report

  • Dr. Lalit Mohan Bhardwaj DNB PGT, General Medicine, Guwahati, Assam, India
  • Dr. P. C. Bhattacharyya Senior Consultant, Department of Medicine, Down Town Hospital, Guwahati, Assam, India
  • Dr. Swapnav Borthakur Senior Consultant, Department of Medicine, Down Town Hospital, Guwahati, Assam, India
  • Dr. Anuj Sarma Senior Consultant, Department of Anaesthesia and Critical Care, Down Town Hospital, Guwahati, Assam, India
  • Dr. Sumitav Barua Senior Consultant, Department of Medicine, Down Town Hospital, Guwahati, Assam, India
Keywords: Isolated ACTH deficiency, Hyponatremia, IAD, Secondary adrenal insufficiency

Abstract

Non-specific symptoms such as asthenia, anorexia, unintentional weight loss, nausea/vomiting particularly in the elderly population are often overlooked both by caretakers and physicians. Deteriorating general health and neuro-psychiatric symptoms are often attributed to depression in the elderly population. The most common electrolyte abnormality, hyponatremia is again more common in the elderly population. Often neglected chronic hyponatremia remains asymptomatic in many cases. Once hyponatremia is detected clinicians should establish a proper diagnosis before supplementation. Failure to diagnose such cases will lead to repeated hospitalization, poor quality of life, wastage of resources and even death. Isolated ACTH deficiency (IAD) is a rare disorder and potentially fatal. IAD can present rarely as hyponatremia and diagnosis can easily be missed if not suspected. IAD may not be as rare as earlier thought as more and more such cases are been reported. Here we report two cases of generalized weakness and nausea; they were repeatedly hospitalized and treated for hyponatremia and ultimately diagnosed as IAD in our hospital.

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References

Dillard GM, Bodel P. Studies on steroid fever II. Pyrogenic and anti-pyrogenic activity in vitro of some endogenous steroids of man. Journal of Clinical Investigation. 1970;49(12):2418-2426. doi: https://doi.org/10.1172/JCI106461.

Goto Y, Tatsuzawa K, Aita K, et al. Neurological symptoms in a patient with isolated adrenocorticotropin deficiency: case report and literature review. BMC Endocrine Disorders. 2016;16:2. doi: https://doi.org/10.1186/s12902-015-0082-6.

Michael Y. Torchinsky, Robert Wineman, and George W. Moll, “Severe Hypoglycemia due to Isolated ACTH Deficiency in Children: A New Case Report and Review of the Literature,” International Journal of Pediatrics, vol. 2011. doi: https://doi.org/10.1155/2011/784867

R. C. Page and F. Alford, Adrenocorticosteroid deficiency: an unusual cause of fever of unknown origin. Postgrad Med J. 1993 May; 69(811): 395–396.

Abhay Gundgurthi, MK Garg, MK Dutta, R Pakhetra. Intramuscular ACTH Stimulation Test for Assessment of Adrenal Function. J Assoc Physicians India 2013 May; 61(5):320-4.

Saepudin et al. BMC Cardiovascular Disorders (2015); 15:88. Doi: https://doi.org/10.1186/s12872-015-0082-5.

Stacpool P. W., Interlandi J. W., Nicholson E., and Rabin D.. 1982. Isolated ACTH deficiency; a heterogeneous disorder. Critical review and report of four new cases. Medicine (Baltimore). 1982 Jan; 61(1):13–24.

Two Cases of Isolated ACTH Deficiency Presenting As Hyponatremia - Case Report
CITATION
DOI: 10.17511/ijmrr.2017.i08.09
Published: 2017-08-31
How to Cite
1.
Bhardwaj LM, Bhattacharyya PC, Borthakur S, Sarma A, Barua S. Two Cases of Isolated ACTH Deficiency Presenting As Hyponatremia - Case Report. Int J Med Res Rev [Internet]. 2017Aug.31 [cited 2024Dec.23];5(8):825-8. Available from: https://ijmrr.medresearch.in/index.php/ijmrr/article/view/916
Section
Case Report