We studied 21 HIV-associated lymphomas with cutaneous presentation to deter
mine whether they showed features of primary cutaneous lymphoma arising for
tuitously or whether they represented the cutaneous involvement of AIDS sys
temic lymphoma. Besides rare mycosis fungoides (n = 3), which shared typica
l clinicopathologic lesions, nonepidermotropic large-cell lymphomas (n = 18
) were predominant. They frequently presented as a solitary nodule or tumor
. Seven of the eight large T-cell lymphomas had a CD30-positive (CD30+) phe
notype but did not express ALK protein. Overexpression of p53 protein was o
bserved in six cases. Although EBV-EBER transcripts were detected in two of
them, LMP1 protein was absent. Except for their original prevalence, the f
eatures of these T-cell CD30+ cutaneous lymphomas were the same as in immun
ocompetent patients. The 10 B-cell cutaneous lymphoma were immunoblastic or
centroblastic lymphomas, with a differential expression of BCL-6 and Synde
can. Four of them expressed CD30, EBER-EBV transcripts, and LMP1 and p53 pr
oteins. This B-cell CD30+ EBV+ phenotype contrasts with cutaneous lymphoma
in immunocompetent patients. Human herpesvirus 8 was not involved in lympho
magenesis since its sequences were detected in a single patient with Kaposi
's sarcoma and Castleman's disease. These lymphomas occurred in severely im
munocompromised patients with a low CD4 count. Death was due to immunodepre
ssion rather than to lymphoma spread, suggesting avoiding aggressive immuno
suppressive treatment in such patients.