Background: Inflammation of retinal vessels is a known association of syste
mic tuberculosis. Patients with retinal vasculitis are subjected to extensi
ve but unrewarding systemic workup. Polymerase chain reaction (PCR) is now
commonly used to detect DNA of infective organisms including Mycobacterium
tuberculosis. This study was undertaken to characterize the clinical charac
teristics of PCR-positive tubercular retinal vasculitis, so as to determine
the clinical presentation, associated systemic features, management, and c
ourse of this form of vasculitis.
Methods: The clinical records of 13 patients seen between 1997 and 1999 wit
h the diagnosis of PCR-positive tubercular retinal vasculitis from the aque
ous or vitreous humor were reviewed. Recorded data included age, sex, race,
visual acuity, anterior and posterior segment findings, and results of dia
gnostic evaluations. All received antituberculosis therapy with or without
concomitant corticosteroids. Laser scatter photocoagulation was done in eye
s with neovascularization. One eye with vitreous hemorrhage was subjected t
o pars plana vitrectomy.
Results: There were 9 (69.2%) male and 4 (30.7%) female patients with a med
ian age of 20 years. The disease was bilateral in seven. The most consisten
t finding was the presence of vitritis in all the eyes followed by vitreous
snowball opacities in 17 eyes (89.4%), neovascularization in 11 eyes (57.8
%), retinal hemorrhages in 10 eyes (52.6%), neuroretinitis in 10 eyes (52.6
%), focal choroiditis in 9 eyes (47.3%), vitreous/preretinal hemorrhage in
5 eyes (26.3%), and serous retinal detachment in 3 eyes (15.7%). Over a med
ian follow-up of 12 months, all showed resolution of vasculitis with no rec
urrences.
Conclusions: Polymerase chain reaction-positive tubercular retinal vasculit
is had varied associated fundus findings. Its recognition is important so a
s to order only relevant diagnostic tests.