Abstract:
Fistula in ano is one of the commonest ailments pertaining to the ano-rectal area and said to arise from
crypto glandular infection of the anal gland, which lies within the intersphincteric space.
Infection would seem to be an integral part of the pathogenesis of fistula in ano. The microbiology of
acute anorectal sepsis is well documented, but the studies on chronic anal fistula have continuously
raised doubts about the relevance of infection in fistula persistence. The present histological study
complements the earlier work, which used microbiological methods alone where important organisms
might have been overlooked.
Granulation tissue from twenty patients with non specific fistula in ano was processed within 4h of
medicated seton (Kshara sutra) therapy. Three samples from the intersphincteric part of the fistula
were obtained.Two samples were studied microbiologically. The pus smear was taken from the
fistulous opening by sterile cotton swab and sent to the Department of Microbiology, in a sterile
container, and pus culture was done. Pus swab was inoculated on nutrient agar medium. The plated
media were incubated at 37 C and examined at 48, hours. Smears from colonies that grew on the
nutrient agar media were stained with Gram-stain. Gram-positive organisms and Gram-negative
organisms were identified by conventional biochemical techniques. The third sample was fixed in 10
per cent formal saline for histological processing. Multiple 4 μm paraffin sections were stained using
haematoxylin and eosin, gram, cresyl fast violet, periodic acid – Schiff and Ziehl – Neelsen stains.
The results show the incidence of fistula in ano and the origin of the predominant microorganism
present in ano rectal fistula. These were investigated using 100 pus samples obtained from the 20
patients.Isolates of Staphyloccus aureus, streptococus Spp and Corynebactrium spp. were identified
as skin derived organisms. Isolates of Enterococcus spp., Escherichia coli, Bacteriodes spp were
considered gastro intestinal tract derived organisms. No mycobacterium species was grown from any
of the eight specimens.
Sections of tissue from all twenty specimens showed a similar pattern of intense active chronic
inflammatory change characterized by a large number of plasma cells, scattered multinucleate
foreign-body giant cells and prominent vascular proliferation. Acute inflammatory change (of
variable degree) was superimposed. No granulomas were seen in any specimen. Vegetable matter
was demonstrated on the granulation tissue surface in one specimen only and bacteria were seen on
histological examination and subsequent Gram staining. Relatively large numbers of organisms were
grown from specimen. Stains for Helicobacter species, mycobacterium tuberculosis and fungi were
negative in all specimens.
The present study has confirmed the relative paucity of organisms and demonstrates through micro
biological study but the histological examination does not reveal many organisms. In fact, i9t is
difficult to obtain a detailed picture through microbiological examinations. But details of the
inflammatory changes can be witnessed through histological examination. In other circumstances,
histological examination has been used to demonstrate important pathogens such as tuberculosis,
Mycobacterium leprae and Helicobacter Pylori.