Background: The cutaneous lesions in chronic lupoid leishmaniasis rese
mble those of lupus vulgaris, both clinically and histologically. The
differential diagnosis is difficult and may depend on the detection of
a few Leishmania amastigotes in the histologic sections, the growth o
f the promastigotes in cultures, or the identification of amastigotes
by other techniques. Polymerase chain reaction was used to detect Leis
hmania amastigote DNA in tissue samples obtained from 65 patients with
chronic lupoid leismaniasis, and the results were confirmed by Southe
rn blot analysis. Observations: The histologic findings of a predomina
ntly epithelioid cell granuloma surrounded by lymphocytic infiltrate i
n chronic lupoid leishmaniasis are very similar to those observed in l
upus vulgaris. Extensive histologic examination of the sections in thi
s series revealed occasional macrophages containing a few amastigotes
in only 12 cases. Cultures in NNN medium yielded Leishmania promastigo
tes in 20 cases. Polymerase chain reaction studies using a Leishmania-
specific primer identified Leishmania DNA in 30 of 63 cases, and those
using a Mycobacterium tubeuculosis primer were found to be negative f
or mycobacteria in 47 cases tested, including 11 cases with a positive
tuberculin skin reaction. Conclusions: The histologic findings in chr
onic lupoid leishmaniasis resemble those of lupus vulgaris. Polymerase
chain reaction studies were useful in identifying amastigotes in 30 (
47.6%) of 63 cases. This study confirms the presence of DNA molecules
of Leishmania amastigotes in samples of formalin-fixed, paraffin-embed
ded granulomatous tissue obtained from patients with chronic lupoid le
ishmaniasis.