| V. RAMÍREZ-AMADOR1, G. ANAYA-SAAVEDRA2, G.
MARTÍNEZ-MATA1-3, I. GONZÁLEZ-RAMÍREZ1, O. PAES DE ALMEIDA2.
1Health Sciences Department México City, Universidad Autónoma
Metropolitana-Xochimilco (UAM-X), México-D.F. 2Oral Pathology Laboratory,
School of Dentistry of Piracicaba-Unicamp, São Paulo- Brazil. 3School of
Dentistry, Universidad Autónoma de Chihuahua, Chihuahua, México.
Objective: The aim of the present study was to identify
and quantify the positive HHV-8 and cytomegalovirus (CMV) cells and its
association with the histological stages of oral Kaposi´s sarcoma (OKS).
Methods: Retrospective, observational and comparative
study. Oral KS cases came from AIDS patients, who attended a referral center
for HIV-infected patients in Mexico City. The median age of the 39 OKS male
patients included was 30 (range, 23-70) years, 25 (64.1%) were under
combined antiretroviral therapy, with a median time of 62.5 (14-369) days.
OKS tissue samples retrieved from the files of the Oral Pathology
Laboratory, UAM-X, were histologically reviewed and classified in early,
intermediate, and late stages. Sections from formalin-fixed
paraffin-embedded archival tissue blocks were analyzed by
immunohistochemistry using antibodies for HHV-8 (LANA-1) and CMV. The
percentage of positive cells for HHV-8 was calculated using a 40x microscope
objective. Photomicrographs were taken from five randomly selected fields
per case, subsequently transferred to a grid and the number of cells
counted. The labelling index of positive cells was calculated for each case.
Expression of CMV was considered as negative or positive. Chi-square test
and the Wilcoxon-Mann-Whitney rank sum test were applied.
Results: Fourteen OKS cases were mucocutaneous (35.9%);
palate was involved in 70.6%. The median CD4+ count was 112 (Q1-Q3,
36.5–166.2) cell/mm3, the median viral load was 2510 (Q1-Q3, 359.7–197500)
copies/ml. The percentage of HHV-8 positive cells increased significantly
from early/intermediate (15.4±10.4) to late (24.5±15.9) (p≤0.05) stages.
Only two cases of late-stage OKS presented infection by CMV; in one of them,
CMV inclusion bodies were present in spindle and acinar cells of minor
salivary glands.
Conclusions: The role for HHV-8 was confirmed through the
progressive increase in the number of positive cells from early/intermediate
to late lesions; however, no evidence supported an active role of CMV in the
pathogenesis of KS. This work was supported by the State of São Paulo
Research Foundation (FAPESP), CNPq (grant #471937/2006-1) and the
Universidad Autónoma Metropolitana-Xochimilco. |