Indian Journal of Endocrinology and Metabolism (Jan 2013)

Primary adrenal insufficiency in case of antiphospholipid syndrome

  • Debmalya Sanyal,
  • Moutusi Raychaudhuri

DOI
https://doi.org/10.4103/2230-8210.119590
Journal volume & issue
Vol. 17, no. 7
pp. 252 – 253

Abstract

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Addison′s disease or primary adrenal insufficiency (PAI) is a rare manifestation of antiphospholipid syndrome (APS). PAI is the most common among the endocrinologic manifestations and can also rarely be the presenting symptom of APS. Venous thrombosis and/or adrenal hemorrhage are the leading cause of PAI in APS. Autoimmune adrenal failure is postulated to be another possible mechanism. We report a case of PAI in a 44-year-old lady preceding primary APS, probably autoimmune, without any evidence of adrenal hemorrhage or infarction. High index of clinical suspicion for PAI in APS is needed; conversely APS should be considered as a possible pathogenetic process in patients presenting with Addison′s disease where the etiology is not obvious.

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