Though the primary site of tuberculosis is lung, it can virtually affect any organ
of the body. The gastrointestinal tract is the sixth most frequent site of extrapulmonary
involvement. Apart from the gut, the peritoneum, abdominal lymph nodes, and more rarely,
the solid organs liver, pancreas, and spleen may be infected with tuberculosis. The
most common site of involvement of the gastrointestinal tuberculosis is the ileocecal
region followed by ascending colon, jejunum, appendix, duodenum, stomach, esophagus,
sigmoid colon, and rectum.
In the study “clinical, imaging, and endoscopic profile of patients with abdominal
tuberculosis” by Shafiq et al,[1] the author has reported a single center experience of 76 cases of abdominal tuberculosis
over the study period of 3 years. This is consistent with the statistics that India
has the world's largest number of tuberculosis cases which is around 26% of the world
TB cases, followed by China and South Africa.[2] Most of the findings in this study are consistent with the earlier reports but for
slight male preponderance.
The incidence of TB in developed countries too is on the rise due to the increasing
prevalence of immunocompromised individuals mainly due to the pandemic of acquired
immunodeficiency syndrome (AIDS) and changed demography with growing immigrant's population.[3] The burden of extrapulmonary tuberculosis is estimated to range from 15 to 20% of
all TB cases in HIV-negative patients, while in HIV-positive subjects, it accounts
for 40 to 50% of new TB cases.[4]
Extrapulmonary TB is not so commonly seen as pulmonary TB and often eludes early diagnosis
until it is late. The late diagnosis is due to its nonspecific clinical presentation.
The symptoms of vague pain in abdomen, diarrhea, and occasional fever are too nonspecific
to suggest the diagnosis unless the treating physician has a high degree of suspicion.
Most often such diagnosis comes to mind when the patient presents either with features
of malabsorption or complications of obstruction in the presence of stricture causing
narrowing of the lumen of ileum.
The patient symptoms of TB of the gastrointestinal (GI) tract vary depending on the
organ involved. A patient may rarely present with dysphagia, odynophagia, and a mid-esophageal
ulcer due to esophageal tuberculosis, dyspepsia and gastric outlet obstruction due
to gastroduodenal tuberculosis, lower abdominal pain and hematochezia due to colonic
tuberculosis, and annular rectal stricture and multiple perianal fistulae due to rectal
and anal involvement.
The Diagnostic Conundrum of Crohn's Disease and Intestinal TB
The Diagnostic Conundrum of Crohn's Disease and Intestinal TB
Differentiating intestinal tuberculosis from Crohn's disease (CD)[5] is an important clinical challenge of considerable therapeutic significance. The
presence of either an active or old pulmonary lesion suggestive of tuberculosis may
be helpful in such situation. In this study, 25 patients (32.8%) showed concomitant
pulmonary findings, while previous studies have documented approximately 15 to 25%
of cases with abdominal TB to have concomitant pulmonary findings. The presence of
ascites offers another avenue for diagnosing tuberculosis. In this study, 30 patients
with ascites showed high protein, low serum ascites albumin gradient (SAAG) ascites,
adenosine deaminase (ADA) was elevated in 23 patients (> 33 U/L), two patients showed
AFB on smear, and none of them grew AFB on culture.
Both tuberculosis (TB) of the gastrointestinal tract and Crohn's disease (CD) are
chronic granulomatous disorders with similarities in their clinical presentation and
pathology.[4] The problem is of greatest magnitude in countries like India where tuberculosis
continues to be endemic and on the other hand, the incidence of CD is on the rise.
Abnormalities in differential leukocyte count, anemia, raised ESR and C-reactive protein
are noticeable in the active phase of both intestinal TB and CD. The ELISA against
anti-Saccharomyces cerevisiae antibody (ASCA) in serum is not specific either.
The Xpert MTB/RIF assay[6] has low sensitivity but high specificity for intestinal TB, and may be helpful in
endemic tuberculosis areas, when clinicians are faced with difficulty differentiating
TB and CD. Based on the Xpert MTB/RIF assay, the prevalence of intestinal multidrug-resistant
TB (MDR-TB) is low in the Indian population. Mycobacteria growth indicator tube (MGIT)
culture is now the standard of care as its yield is superior to that of the traditional
Lowenstein–Jensen medium. Increasing the number of colonoscopic biopsy samples for
mycobacteria growth indicator tube (MGIT) culture can increase the yield.
Culture and histopathology are complementary. Although culture gives a definitive
diagnosis, to get the result usually takes weeks. Even then a positive diagnosis of
intestinal TB may remain elusive in a significant proportion of patients. Scoring
systems with specificity of 90 have been developed but their utility in routine practice
is yet to be established. Similarly, the value of polymerase chain reaction (PCR)
in arriving at the diagnosis is uncertain.
Gene Xpert in a molecular test for TB, which diagnoses TB by detecting the presence
of TB bacteria, as well as testing for resistance to the drug rifampicin. In India,
this test is known as the cartridge based nucleic acid amplification test (CB-NAAT).
It has been found to be useful in the diagnosis of pulmonary TB and its utility in
intestinal TB needs to be looked at.
Useful modalities for investigating a suspected case include a contrast-enhanced computed
tomography study (CECT) of abdomen, ultrasonography, and colonoscopy. Ascitic fluid
examination reveals straw colored fluid with high protein, SAAG less than 1.1 g/dL,
predominantly lymphocytic cells, and ADA levels above 36 U/L. Sometimes diagnostic
laparoscopy is a very useful investigation in doubtful cases.
Despite the best efforts and investigations, the diagnosis of abdominal TB can still
be elusive. In such situations, taking into consideration the symptoms and overall
clinical picture, the clinician may proceed to start antituberculosis treatment (ATT)
empirically and the patient is closely followed. If the patient shows improvement
of symptoms and starts gaining weight, it is obvious the treatment is on the right
track. In this study, five patients were started on empiric antitubercular therapy
(ATT) as there was diagnostic dilemma due to discordance in clinical and laboratory
findings, and fortunately all five patients exhibited a rapid response to ATT.
Treatment
Abdominal TB generally responds to medical treatment alone and surgery is usually
reserved for those cases with complications like obstruction due to stricture, abscess,
or where there is a fistula. Early diagnosis and treatment can prevent unnecessary
surgical intervention. Even in cases of tuberculous strictures,[7] medical management with antituberculous drugs will result in significant resolution
of symptoms in most of the patients. Endoscopic balloon dilation offers an alternative
to the surgical management of GI stricture
Antituberculous therapy is usually for 6 months, which includes initial 2 months of
therapy with isoniazid (INH), rifampicin (RMP), pyrazinamide (PZA), and ethambutol
(EMB) followed by a further 4 months course with RMP and INH. Cochrane researchers
examined the available evidence up to the September 2, 2016 and concluded that 6-month
regimens are probably as good as 9-month regimens in terms of numbers of people cured
but more studies are needed for making confident conclusions.[8]
Drug toxicity is a point of concern which requires a close follow up. In this study,
eight patients (10.5%) developed hepatotoxicity due to ATT, seven out of whom tolerated
either sequential reinitiation of ATT or modified ATT. One patient had to be referred
to a tertiary liver center due to development of acute liver failure (ALF). Drug resistance
is increasingly common in strains of mycobacterium tuberculosis (MTB) and may contribute
to recurrence or persistent disease.
