Hypothesis: Rhinosinusitis is common during HIV infection; its prevalence i
s uncertain and could probably be related to clinical features, immunoaller
gological status, and diagnostic criteria. Methods: Seventy-four patients h
ospitalized with HIV infection were prospectively evaluated for the presenc
e of rhinosinusitis based on clinical findings, nasal endoscopy, or paranas
al sinus computed tomography (CT), Immune status, nasal smear, features of
atopy (based on the prick test), and its contribution to sinusal inflammato
ry pathology were also evaluated. Results: Most patients were severely immu
nosuppressed: CD4+ 155 +/- 201 cells/mL and 12 +/- 11% (mean +/- SD), Thirt
y-five percent of the patients presented at least two criteria of rhinosinu
sitis (clinical findings, nasal endoscopy, and CT: 35%; clinical findings a
nd CT: 50%; nasal endoscopy and CT: 15%). CT scan showed multiple sinus inv
olvement, opacification over 25% of the total volume of the maxillary sinus
in 50% of patients, and opacification of the sphenoidal sinus in 40% of ca
ses. Atopy was present in 18% of patients, a figure which reflects the expe
cted prevalence in our geographic area. Two independent predictors were ass
ociated with a higher probability of rhinosinusitis: bilateral absence of m
axillary infundibular patency (odds ratio, 7.5; 95% CI = 2.03-27.9) and low
total count (odds ratio, 0.99; 95% CI = 0.99-1.00) or percentage of CD4+ (
odds ratio, 0.93; 95% CI = 0.88-1.00). Conclusions: There is a high prevale
nce of rhinosinusitis in HIV-infected individuals. This finding is related
to a decreased cellular immunity, but it does not appear to be related to I
gE-related immediate hypersensitivity. Nasal endoscopy should be the first-
step diagnostic test. However, when clinical suspicion exists and endoscopy
fails to explain symptoms, CT scan is a valuable adjunct to establish this
diagnosis.