Viral infection in children commonly causes acute lung disease leading
to respiratory decompensation requiring intensive supportive therapy.
Definitive diagnosis of the causative virus may be difficult, relying
on serologic data since viral cultures are frequently negative; lung
biopsy may be necessary to increase the diagnostic yield, The objectiv
e of this study was to develop a rapid and sensitive diagnostic method
using the polymerase chain reaction (PCR). Analyzing Formalin-fixed l
ung tissue from autopsies of 32 patients with pneumonitis in whom cult
ures, serology, and histopathology results were blinded to the investi
gators, and 10 negative control samples, PCR was performed for cytomeg
alovirus, adenovirus, enteroviruses, herpes simplex virus, and Epstein
-Barr virus, Among the 32 affected specimens, 7 were culture-positive
for a specific virus in the lung; 6/7 of these were PCR-positive for t
he identical virus, In the culture-positive specimen not PCR amplified
, influenza B was the cultured agent, but this virus was not evaluated
by PGR, In the remaining 25 samples which were culture-negative, 11 w
ere PCR-positive. All 10 negative controls were negative by PCR. Three
specimens with CMV inclusions but culture-negative were also negative
by PCR, We conclude that PCR is sensitive and accurate in the evaluat
ion of lung tissue for viral pneumonitis. (C) 1996 Academic Press, Inc
.