De. Alcantarapayawal et al., DIRECT-DETECTION OF MYCOBACTERIUM-TUBERCULOSIS USING POLYMERASE CHAIN-REACTION ASSAY AMONG PATIENTS WITH HEPATIC GRANULOMA, Journal of hepatology, 27(4), 1997, pp. 620-627
Background: In liver tuberculosis, demonstration of acid bacilli by co
nventional methods remains futile, Since the definitive diagnosis of l
iver tuberculosis is based on the histologic evidence of granulomatous
process with caseation necrosis, seen in only a third of cases, the d
iagnosis is made retrospectively by response to empirical anti-tubercu
lous drug therapy. Aims: Our objective is to establish a polymerase ch
ain reaction assay for detection of Mycobacterium tuberculosis affecti
ng the liver using the paraffin-embedded liver biopsy specimens obtain
ed from patients with hepatic granulomas. Methods: As positive control
, patients having either ''definitve'' (n=8) or ''presumptive'' (n=9)
tuberculosis on the basis of clinical, microbiological, histologic dat
a and their positive response to empirical treatment of anti-tuberculo
us drugs were used, Patients with hepatic granulomas secondary to schi
stosomiasis (n=6), sarcoidosis (n=2) and other liver diseases (n=10) w
ere used as negative control. Results: Of those patients who were diag
nosed as having ''definitive'' and ''presumptive'' liver tuberculosis,
positivity by one-step polymerase chain reaction was 100% and 44%, re
spectively, Using the nested polymerase chain reaction, positivity inc
reased to 78% with ''presumptive'' liver tuberculosis, In contrast, th
e polymerase chain reaction assays were negative among all patients wi
th hepatic granuloma due to non-tuberculous-in-origin and other liver
diseases. Conclusions: The overall positivity of this polymerase chain
reaction assay (88%) compares favorably with that of other convention
al methods (12%), Thus, this polymerase chain reaction assay may be a
reliable diagnostic tool for liver tuberculosis in a patient populatio
n in which the prevalence of diseases associated with hepatic granulom
a is common.