AI Article Synopsis

  • Hypercalcemia in HIV patients can arise from different mechanisms, especially due to elevated levels of 1,25-dihydroxycholecalciferol (1,25 (OH)2 vitamin D) often linked to diseases like Mycobacterium avium intracellulare (MAI).
  • A case of late-onset hypercalcemia was reported in an HIV/AIDS patient with MAI, which was correlated with the immune reconstitution inflammatory syndrome (IRIS), despite normal levels of vitamin D metabolites.
  • The situation highlights the need to consider IRIS when diagnosing late-presenting hypercalcemia in HIV patients, as timely steroid treatment can be effective in managing the condition.

Article Abstract

Hypercalcemia in human immunodeficiency virus (HIV) patients can be challenging due to various underlying mechanisms. 1,25- dihydroxycholecalciferol (1,25 (OH)2 vitamin D)-mediated hypercalcemia due to increased activity of extrarenal 1-alpha hydroxylase is one of the well-known mechanisms of hypercalcemia described in HIV patients. (MAI) is a granulomatous disease that can cause hypercalcemia due to ectopic production of alpha -1 hydroxylase and result in increased levels of 1,25 (OH)2 vitamin D. Herein, we present a case of "late-onset" hypercalcemia in a patient with HIV/AIDS and MAI infection in the setting of suspected immune reconstitution inflammatory syndrome (IRIS). The hypercalcemia workup showed an inappropriately average level of 1,25 (OH)2 vitamin D while the rest of the workup was unrevealing. Unusually normal levels of vitamin D metabolites were the driving mechanism of hypercalcemia in this case. The late presentation of hypercalcemia was likely due to IRIS unmasking an underlying granulomatous infection, and this consideration led to the successful treatment of the patient with steroid administration. This case emphasizes the importance of considering IRIS in evaluating hypercalcemia that presents late in the course of granulomatous infections in HIV patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11075998PMC
http://dx.doi.org/10.7759/cureus.57773DOI Listing

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