Av. Kravchenko et al., Kaposi's sarcoma in HIV-infected patients: clinicolaboratory manifestations, therapeutic approaches., GEMATOL TR, 45(1), 2000, pp. 25-28
Kaposi's sarcoma (KS) develops in 20% of AIDS patients who are, as a rule,
of young or middle age (20-50-year-olds). In most cases the disease is rapi
dly progressive up to visceral involvement, presents with rare forms, is ac
ute, number of CD4+ and B-lymphocytes is very low against very high content
of IgA, IgG and CIC. Half of the patients with AIDS-associated KS had symp
toms of moderate DIC syndrome (low count of platelets with normal function)
. Lethal outcome was due to addition of opportunistic infection. Treatment
policy should account for severity of immune system impairment and presence
of opportunistic infections. High-dose intron A combined with AZT is rathe
r effective and minimally affects hemostasis and immunity in patients with
severe HIV-infection and KS.