Tissue specimens from a wide variety of anatomic locations are frequen
tly examined for mycobacteria using a combination of cultures and spec
ial stains. Auramine-rhodamine (AR) staining is a sensitive method for
detecting acid-fast bacilli (AFB) in tissue sections. We reviewed 85
AR-positive and 275 randomly selected AR-negative biopsy specimens col
lected during the past 2 years at the Mayo Clinic, Rochester, Minn. Pa
thologic diagnoses and culture results were also reviewed. Biopsy spec
imens containing necrotizing granulomas yielded the highest positivity
rate for AFB (61 [47.7%]), followed by nonnecrotizing granulomas (14
[17.7%]). Poorly formed granulomas (5 [16.1%]) and acute inflammation
(5 [15.6%]) were less frequently positive. Cases with fibrotic or hyal
inized granulomas, nonspecific chronic inflammation, nonspecific react
ive or reparative changes, no significant histologic abnormality, or m
alignancy failed to disclose AFB. These specimens, which were consiste
ntly negative for AFB, were responsible for 25% of the samples submitt
ed. Of the 360 tissue specimens submitted, 166 had a corresponding myc
obacterial culture. Mycobacteria were cultured only from the biopsy sp
ecimens that contained necrotizing granulomas (38.2%), nonnecrotizing
granulomas (32.4%), poorly formed granulomas (30.0%), or acute inflamm
ation (15.8%). Tissues with fibrotic or hyalinized granulomas, nonspec
ific chronic inflammation, nonspecific reactive or reparative changes,
no significant histologic abnormality, or malignancy failed to yield
positive cultures. These data suggest that biopsy specimens with these
latter diagnoses are inappropriate specimens for mycobacterial cultur
e or AR staining.