Dm. Munger et al., ACUTE ADDISON CRISIS DUE TO HISTOPLASMOSI S OF THE ADRENAL-GLANDS, Schweizerische medizinische Wochenschrift, 124(48), 1994, pp. 2188-2195
A 44-year-old man was admitted with symptoms compatible with Addison c
risis. Abdominal computer tomography revealed extensive bilateral adre
nal abscesses. Histoplasma capsulatum was cultured from a needle aspir
ate. The patient was HIV-seronegative and had no underlying malignancy
. He may have acquired the infection during several stays in endemic a
reas in the United States, South America and Asia. The case was also r
emarkable for moderate brain atrophy, thrombosis of the portal and spl
enic veins and liver cirrhosis caused by alpha-1-antitrypsin deficienc
y (phenotype MZ). The patient recovered fully under substitution of ad
renal hormones and antifungal treatment. He received intravenous ampho
tericin B (75 mg q24h) for 10 days, followed subsequently by oral trea
tment with itraconazole (400 mg q24h) over several months. Radiologic
follow-up 9 and 18 months later showed a pronounced decrease of the in
flammatory adrenal lesions.