Background Disseminated histoplasmosis usually occurs in immunocompromised
patients who reside in Histoplasma capsulatum-endemic regions. It has also
been described in immunocompetent infants after exposure to a large inoculu
m of the pathogen resulting in case fatality rates of 40 to 50%,
Methods, From 1983 through 1996 all infants with documented disseminated hi
stoplasmosis were treated with amphotericin B followed by daily ketoconazol
e for 3 months. Immunologic workups were performed at the time of diagnosis
and at 4 to 6 weeks of therapy. Surviving patients were followed for at le
ast 1 year, Time to resolution of signs and symptoms was recorded, as were
complications.
Results, We managed 40 patients with disseminated histoplasmosis. The age i
n months at diagnosis was 15.3 +/- 10.2 (mean +/- SD), and 24 were male. Al
l patients were from endemic regions and they presented with fever, spleen
and/or liver enlargement and hematologic abnormalities. Diagnosis was made
by histology and culture of bone marrow, spleen, lymph node, bronchoalveola
r or liver samples. Twenty patients presented with T cell deficiency that r
esolved at 4 to 6 weeks of therapy in all of the retested patients, and 10
of 12 tested patients had hyperglobulinemia that resolved. Thirty-five (88%
) patients were cured by treatment; 4 died and 1 relapsed,
Conclusions. Disseminated histoplasmosis should be considered in infants fr
om endemic areas who present with fever, hepatosplenomegaly and hematologic
abnormalities, These patients develop transient hyperglobulinemia and T ce
ll deficiency that resolve with treatment. Treatment with amphotericin B fo
llowed by an oral azole for 3 months is effective in most patients.