“…However, numerous case reports describe individuals with objectively normal immune function who nonetheless have clinical or pathological evidence of primary adrenal involvement in the setting of an indolent infection. [2][3][4][5][6][7][8][9][10][11][12][13][14][15][16] Due to the non-specific nature of the symptomatology and laboratory manifestations (e.g., fatigue, anorexia, low blood pressure, hyperkalemia, hypernatremia, hypoglycemia 1 ) and the fact that 80-90% of the gland must be destroyed before the patient will demonstrate overt Addisonian symptoms, 17 antemortem diagnosis is rare. However, prompt recognition combined with appropriate therapy early in the disease course may prove beneficial, 13,15,16,[18][19][20] thereby warranting a high clinical suspicion for adrenal involvement in the appropriate clinical scenario.…”