Visceral leishmaniasis (kala-azar) is a worldwide disseminated protozoal in
fection primarily transmitted by sand flies. Because host defense against t
his intracellular infection is T-cell-dependent, kala-azar has predictably
joined the list of AIDS-related opportunistic infections in endemic areas.
The vast majority of patients with AIDS-associated kala-azar are currently
found in southern Europe (the Mediterranean basin, especially Spain in inje
ction drug users); future cases will inevitably arise in other endemic regi
ons including India, East Africa and Sudan, and Brazil. In CD4 cell-deficie
nt HIV-infected individuals, kala-azar likely represents recrudescence of p
reviously controlled asymptomatic infection; in drug users, newly acquired
infection may result from transmission via shared needles. Coinfected patie
nts are frequently parasitemic and may show atypical clinical presentations
, unusual multi-organ involvement, and absent antileishmanial antibodies. D
iagnosis is made by microscopic examination or culture of aspirate or biops
y of any involved tissue (primarily bone marrow) or by blood smear or cultu
re. Conventional treatment (pentavalent antimonials) induces initial remiss
ion in about 50% of patients; amphotericin B and its new lipid formulations
appear more active. If suppressive maintenance therapy is not used, relaps
e within 1 year is typical. In AIDS patients with a first episode of viscer
al kala-azar, up to 25% die within 1 month if treatment is stopped. Optimal
primary and secondary prophylaxis for AIDS-related kala-azar remain to be
determined; life-long maintenance therapy is becoming an accepted approach.