| J. LI1, Y. HAN1, R. MA2, W. ZHAO1, Y. LIU1,
X. LIU1, H. XING1, Q. ZHAO2, and H. LIU1 1Peking
University School and Hospital of Stomatology, Beijing, China, 2Contagious
Hospital of Henan Province, Beijing, China
Objective: The purpose of this study was to explore the
possibility of diagnosing oral hairy leukoplakia (OHL) by means of a
non-invasive test.
Method: Exfoliative cytology and virus DNA specimens were
obtained from lesions of 40 HIV sero-positive participants, who demonstrated
clinical features of oral hairy leukoplakia. Cytologic smears were processed
according to routine Papanicolaou (PAP) stain procedure for detection of
morphologic changes and periodic acid-Schiff (PAS) stain procedure for
detection of C. albicans hypha invading the parakeratin layer of the
epithium under standard microscopy. DNA was extracted from exfoliative cells
of OHL lesions, on which real-time fluorescent quantitative polymerase chain
reaction (RT-PCR) was used to detect the Epstein-Barr virus (EBV) DNA.
Result: Of the 31 DNA samples, 26 (83.9%) were positive
for EBV DNA. 23 (79.3%) of 29 cases demonstrated condensation and
margination of nuclear chromatin (nuclear beading), while 19 (65.5%) of 29
cases displayed enlarged binucleation or multinucleation. 18 (62.1%) cases
and 24 (82.8%) cases demonstrated either nuclear beading and binucleation or
multinucleation. Compared with RT-PCR positive reaction for EBV DNA, the
sensitivity of PAP stain used for detection of evidence of virus infection
in OHL is 80% (Criteria: either nuclear beading or binucleation or
multinucleation was seen). All of the 5 RT-PCR negative for EBV DNA cases
were suggested having virus infection by PAP stain. C.albicans hyphe were
noted in 83.3% (15/18) cytologic smears.
Conclusion: Noninvasive tests, PAP stain for virus
infection morphologic change, PAS stain for C. albicans infection and
exfoliative cell RT-PCR positive reaction for EBV DNA are efficient methods
to screen for OHL in HIV sero-positive individuals. |