BACKGROUND. Human papillomaviruses (HPVs) commonly cause proliferative
lesions of squamous epithelia, and infection with certain HPV types c
arries a high risk of malignant transformation, especially in the uter
ine cervix but also at other sites, including the esophagus. We used m
olecular techniques to detect and type HPV in an in situ squamous cell
carcinoma in the esophagus of a 39-year-old woman. METHODS. DNA was e
xtracted from paraffin sections of the esophageal lesion and of the ut
erine cervix (which was removed several years earlier), and analyzed f
or HPV by polymerase chain reaction (PCR). Primers complementary to hi
ghly conserved regions of the open reading frame of most genital HPVs
were used to amplify a similar to 150 base pair product that contained
both conserved and divergent regions. The PCR products were hybridize
d with probes specific for HPV-G, HPV-11, HPV-16, and HPV-18, and with
a consensus probe. A conspicuous band in the esophageal sample failed
to hybridize with any of the probes. The amplimer was subcloned and s
equenced. The sequence was compared with other known HPVs. RESULTS. Th
e intraepithelial neoplasia in the patient's cervical cone biopsy cont
ained HPV-16. The esophageal lesion contained HPV that did not hybridi
ze with probes for types 6, 11, 16, or 18, but exhibited 98.3% homolog
y with HPV-73. CONCLUSIONS. Squamous cell carcinoma in situ of the eso
phagus may be associated with infection by HPV-73. (C) 1996 American C
ancer Society.