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ABDOMINAL
TUBERCULOSIS
SYMPOSIUM BY JR-1
UNIT IV, GENERAL SURGERY
SCOPE OF PRESENTATION
 DEFINITION
 HISTORY
 AGENT
 EPIDEMIOLOGY
 ROUTES OF TRANSMISSION &
PATHOGENESIS
 CLASSIFICATION
 INVESTIGATIONS
 MANAGEMENT
 RARE TYPES OF GI
TUBERCULOSIS
 TB IN HIV & PREGNANCY
DEFINITION
The term abdominal tuberculosis refers to tuberculous infection of
the gastrointestinal tract, mesenteric lymph nodes, peritoneum
and omentum, and of solid organs related to the gastrointestinal
tract such as the liver, spleen and pancreas.
HISTORY
 Tuberculosis was first recognised in Fourth century
BC
 Hippocrates described a condition resembling
tuberculosis in a patient with pulmonary lesions and
intestinal disease
 Charles Dickens (1812-70) described TB as:
“Dreaded disease in which there is a gradual and
quiet struggle between soul and body where
mortal part whithers away grain by grain and get
wasted”
 Major cause of intestinal strictures and bowel
obstruction in the 19th century and early part of 20th
century
HISTORY
 1882 – Identification of the
causative organism,
Mycobaccterium tuberculosis,
by Robert Koch
 Formulated Koch’s postulates to
describe the etiology of Cholera
and TB
 1998 – complete genetic
sequence of M. tuberculosis
was identified.
AGENT
 Mycobacterium tuberculosis (90%)
 M. bovis (largely eliminated)
 The tubercle bacilli is :
 Gram positive
 Aerobic
 Non-motile
 Non- spore bearing
 Identified by Ziehl- Neelson acid fast differential
staining method (high content of mycolic acid in cell
wall)
 Culture of organism is in Lowenstein-Jensen
medium : 04-06 weeks
Lowenstein Jensen media showing
growth of Mycobacterium tuberculosis
EPIDEMIOLOGY
 GLOBAL INCIDENECE:
 Among top 10 causes of death globally
 2021 – 6.4 million people developed tuberculosis
 In 2020 – estimated 1.6 million deaths incl 187,000 with
HIV
 1/4th of global population has latent TB infection
 Complicated by emergence of MDR
 India has 26 per cent of World TB cases
 In 2021, TB incidence in India in all forms was
1,933,381 – 19% higher than 2020.
 TB declared as notifiable disease by Govt of India on
09 May 2012
 World TB day : 24 March
EPIDEMIOLOGY
 Common in India & developing countries, more
frequently in people of poor socio-economic
background
 6th most common type of extrapulmonary TB
following LN, pleura, GU tract, bones/joints and
meninges .
 Higher incidence in HIV infected patients : 36% of
AIDS patient develop TB, among which 50 %
develop abdominal TB
0%
10%
20%
30%
40%
50%
60%
70%
80%
90%
100%
PERITONEAL
MENINGEAL
MILIARY
OTHERS
BONE/JOINTS
GU
PLEURAL
EPIDEMIOLOGY
All cases All extrapulmonary cases
Pulmonary TB
3.3%
4.6%
7.3%
9.8%
9.8%
11.9%
23%
30%
EPIDEMIOLOGY
Developed countries
 Immigrant population
 Ageing population
 Increase in HIV
Developing countries
 Incomplete treatment
 MDR strains
 Increase in HIV/AIDS
RE-EMERGENCE
TRANSMISSION
 Ingestion of contaminated food : causing primary
abdominal tuberculosis
 Swallowed sputum : containing tuberculous bacteria from
primary pulmonary focus causing secondary abdominal
tuberculosis.
 Hematogenous spread: during bateremic phase that may
follow primary TB
 Lymphatic spread : from infected nodes (5-10%)
 Direct spread :
 From Fallopian tubes by retrograde spread to involve peritoneum
(10%)
 From adjacent organs
 Disseminated in bile : since they are sequestrated and
excreted from granulomas in liver
PATHOGENESIS
PATHOGENESIS
Bacilli enters GI mucosa
Inflammatory reactions
Bacilli carried to Peyer’s
patches by phagocytes
Tubercle
formation
Submucosal tubercles
enlarge & undergo necrosis
Endarteritis & edema
Sloughing & ulceration
Collagen accumulation
Thickening & stenosis
Penetration of serosa
Tubercles on serosal surface
Bacilli reaches lymphatics
•Bowel & mesenteric
lymphatic obstruction
•Thick, fixed mass
• Regional LN
• Hyperlasia
• Caseation necrosis
• Calcification
TYPES OF ABDOMINAL TUBERCULOSIS
TYPES
1. Intestinal:
 Ileocaecal region:
 Ulcerative (60 %)
 Hyperplastic
 Ulcero-hyperplastic
 Ileal region: commonly
stricture type
2. Peritoneal
 Acute
 Chronic:
 Ascitic type
 Encysted (loculated) type
 Plastic (fibrous/adhesive)
 Purulent type
3. TB of mesentery and its LN
4. Ano-recto-sigmoidal
5. Involvement of organs:
Liver, spleen and other
forms of miliary TB
6. TB of omentum
7.Rare types:
 Oesophageal
 Gastroduodenal
 Retroperitoneal TB
ILEOCAECAL TUBERCULOSIS
 Most common site of abdominal TB
 Due to:
 Stasis : bacterial contact time is more
 Abundant Peyer’s patches
 Minimal digestive activity
 Fluid and electrolyte absorption
 Types:
 Ulcerative 60%
 Hyperplastic
 Ulcero-hyperplastic 30%
ILEOCAECAL TUBERCULOSIS
 Ulcerative
 Common in old, malnourished people
 Circumferential transverse ulcers – with skip lesions
 Long standing ulcers cause fibrosis and later stricture
formation (Napkin- ring structure)
 Bowel adhesions are common
 Mainly presents with diarrhoea, blood in stool, loss of
appetite and reduced weight.
Fig - Ileocaecal Tuberculosis: Note the sites and tubercles
in ileocaecal valve
Fig - Histology of ileocaecal tuberculosis showing Epithelioid cell
granuloma with caseation
 photo
 Hyperplastic:
 10% common, less virulent
 young, well nourished
individual
 Fibroblast reaction in
submucosa and subserosa -
thickening of bowel wall and
LN enlargement, leading to
nodular mass
 Common in caecal part
ILEOCAECAL TUBERCULOSIS
Note the ileocaecal
tuberculosis with stricture.
ILEOCAECAL TUBERCULOSIS
•Causes extensive chronic
inflammation, fibrosis, bowel
adhesions, nodal
enlargement, often presents
with mass in RIF
•When presents as a mass-
SAIO
 Virulent organism
 Poor body resistance, old people
 Multiple transverse ulcers
 Clinically -diarrhea, bleeding P/R,
loss of appetite and reduced
weight
 Complications: stricture, Intestinal
obstruction
 Barium study - ileal strictures
 Less virulent organism
 Good body resistance,
young individuals
 Chronic granulomatous
lesion in ileocaecal region
 Presents as mass in RIF
 Complications: SAIO
 Barium study -pulled up
caecum, obtuse ileocaecal
angle
ULCERATIVE HYPERPLASTIC
ILEOCAECAL TUBERCULOSIS
 Usually stricture type
 May be multiple
 Presents usually with intestinal obstruction, bowel
adhesions, localisation, fibrosis
 Perforation (5%)
ILEAL TUBERCULOSIS
 Pathology:
 Enormous thickening of the
parietal peritoneum with
multiple tiny yellowish
tubercles
 Dense adhesions in
peritoneum and omentum
with content inside as small
bowel looking like Abdominal
cocoon (sclerosing
encapsulating peritonitis).
PERITONEAL TUBERCULOSIS
ACUTE PRESENTATION
 Mimics acute abdomen
 On- table diagnosis
 Presents with features of peritonitis
 Due to perforation or rupture of mesenteric tubercular
LN
PERITONEAL TUBERCULOSIS
 Photo A-C intraop findigns slide 24
Fig A to C - On-table findings in
intestinal tuberculosis,
of extensive involvement with
multiple tiny tubercles, thickening,
adhesions and involvement of
mesenteric lymph nodes.
CHRONIC PRESENTATION
1. Ascitic form (Wet type):
 Distension of abdomen with dilated veins.
 Ascitic tap reveals straw colored fluid from which AFB
can be isolated.
PERITONEAL TUBERCULOSIS
2. Encysted (Loculated) ascites:
 Ascites gets loculated because of the fibrinous
deposition
 Dullness, which is not shifting, is the typical feature
 May present as intra-abdominal mass, which may
mimic ovarian cyst, retroperitoneal cyst or
mesenteric cyst
PERITONEAL TUBERCULOSIS
3. Plastic type (Dry type):
 Widespread adhesions
 Present with colicky abdominal pain, diarrhoea, wasting
and loss of weight, doughy abdomen
 D/D: Peritoneal carcinomatosis
PERITONEAL TUBERCULOSIS
4. Purulent form:
 Invariably due to tuberculous salpingitis
 Presents as mass in the lower abdomen containing pus.
 Cold abscess gets adherent to abdominal wall, umbilicus
and may form an umbilical fistula
 Patient commonly has got genitourinary tuberculosis
PERITONEAL TUBERCULOSIS
TUBERCULOUS MESENTERIC LYMPHADENITIS
 Infection is usually through the Peyer’s patches
 Commonly, right sided LN involved
 Presents with general symptoms, pain in umbilical
region and RIF, mass in RIF or features of acute
appendicitis
 Often coils of intestine get adherent to the caseated
mesenteric LN leading to intestinal obstruction.
 Caseating material may collect between the layers of the
mesentery, forming a cold abscess – pseudomesenteric
cyst.
 Massive enlargement of mesenteric LN due to TB is
called as Tabes mesenterica
Fig - Note the location of mesenteric tuberculous lymphadenitis in
the right iliac fossa. But it can occur anywhere in the line of
mesentery.
TUBERCULOUS MESENTERIC LYMPHADENITIS
Fig A-C: On table finding of
Mesenteric tubercular
lymphadenitis
ABDOMINAL TUBERCULOSIS
 Differential diagnosis:
 CA caecum
 Lymphoma
 Retroperitoneal tumor
 Non specific lymphadenitis
ANO-RECTO-SIGMOIDAL TUBERCULOSIS
 It mimics Carcinoma rectum, most
common symptom - hematochezia
 Presents as tenesmus, diarrhoea,
discharge from fistula and ocassionally
as mass per abdomen
 Fistulas- painful and characteristically
not indurated
 TB fistulas -multiple, shallow, bluish in
color with undermined edges.
TUBERCULOSIS OF OMENTUM
 Usually occurs as a part of the other types
 Characteristic finding - Rolled up omentum with
thickening
 Often cold abscess can develop.
DIFFERENT CLINICAL PRESENTATIONS OF ABDOMINAL
TUBERCULOSIS
 Clinical presentation:
 Acute
 Acute on chronic
 Chronic
 Common in 25-50 yrs age group, equal in both sexes
 Constitutional symptoms:
 Anemia, loss of weight & appetite (80%)
 Diarrhoea (10-20%)
 Fever (50-70%)
 Failure to thrive, in children
 Overall observed in 30% of the patients
CLINICAL PRESENTATIONS
 Abdominal Pain
 Mass in RIF – may mimic Carcinoma caecum
 Other sites of lump:
 Central abdomen – enlarged mesenteric LN
 Ilioinguinal – Iliopsoas abscess secondary to TB spine
 Upper abdomen – rolled up omentum
 Lower abdomen – Tubo-ovarian mass
 Anywhere in abdomen – colonic TB, loculated ascites,
matted bowel loops
 Can be associated with adenocarcinoma of caecum or
large bowel lymphoma or HIV
SUMMARY OF SYMPTOMS AS PER TYPES
Types Symptoms
Ulcerative Diarrhoea and malabsorption
Stricture Subacute or acute intestinal obstruction
Hyperplastic Mass abdomen (RIF) and obstruction
Ascites Generalised distension of abdomen
Localised Intra abdominal mass, may mimic ovarian cyst,
retroperitoneal or mesenteric cyst
Peritoneal Abdominal cocoon, vague abdominal pain
Mesenteric Tabes mesenterica, obstruction, mass
 Atypical presentation:
 Lower GI bleed
 Fistula in ano
 PID like pain
 Gastric disease symptoms, Dysphagia
 GI fistula
INVESTIGATIONS
INVESTIGATIONS
 Hematological & Biochemical:
 Anemia
 Raised ESR, CRP
 Hypoalbuminemia
 Mantoux test
 ELISA IgG
INVESTIGATIONS
 Chest X-Ray: to rule out primary focus
 Straight X-Ray abdomen:
 Intestinal obstruction
 Calcified LN
 Hollow viscus perforation
BARIUM MEAL STUDY
 Barium study X-Ray (Enteroclysis followed by
barium enema or barium meal follow through)
Series of a barium meal and follow-through showing strictures in the ileum, with the
caecum pulled up into a subhepatic position and obtuse ileocecal angle.
BARIUM MEAL STUDY
Conical
caecum
Narrowed
ileum
String sign – persistent narrow stream
 Napkin lesions – ulcers &
strictures in the terminal
ileum and caecum
 Earliest signs – increased
transit time,
hypersegmentation
(chicken intestine),
flocculation of barium
 Mega ileum – multiple
strictures with enormous
dilatation of proximal ileum
Chicken Intestine sign
INVESTIGATIONS
 USG findings:
 Thickened bowel wall, mesentery, omentum, peritoneum
 Loculated ascites with fine septae
 Interloop ascites with alternate echogenic and echo free
areas – Club sandwich appearance
Club Sandwich appearance
USG FINDINGS
 Bowel loop radiates from its mesenteric root –
Stellate sign
 Mesenteric loop thickness more than 15 mm
 Hepatosplenomegaly
 LN enlargment, matted
 Pulled up caecum presenting as a mass in
subhepatic region – Pseudokidney sign (also seen
in intususception)
 Concentric uniform mural thickening
 CT abdomen:
 Very useful and reliable
 Findings:
 Thickened bowel wall, peritoneum
 Ileocecal valve thickening
 Enlarged/necrosed/ matted mesenteric nodes,
often with cold abscess
 Adhesions
 Mesenteric thickening and nodules
 Nodules in peritoneum/ solid organs
 Adhesions in the bowel/ stricture/ obstructive
features
 Loculated ascites
 CT guided FNAC / biopsy/ fluid aspiration
INVESTIGATIONS
COLONOSCOPY
 To rule out CA
 Shows mucosal nodules, ulcers,
strictures, deformed ileocecal
valve, mucosal oedema and
diffuse colitis
 Biopsy can be taken to establish
diagnosis
 Capsule endoscopy : useful to
see small intestinal pathology in
difficult cases due to obstruction
at stricture site.
 Laparoscopy :
 Aids in visualisation
 To collect ascitic fluid for analysis
 To take biopsy
 Blind percutaneous needle peritoneal biopsy
 Using Cope’s / Abraham’s needle
 Ascitic tap for fluid analysis
 BACTEC MGIT broth culture
INVESTIGATIONS
NEWER SEROLOGICAL INVESTIGATIONS
 IFN gamma release assay (IGRA) : based on
detection of IFN gamma released by sensitied T cells
on stimulation with specific Ags.
 T spot TB test – directly count the no. of IFN gamma
secreting T cells
 Quantiferon TB Gold in-tube test – measures the
concentration of IFN gamma secretion
 Early secretory Antigen Target-6 (ESAT-6) & Culture
filtrate protein-10 (CFP 10):
 Both derived from a very specific region of MTb, the region
of difference 1 (RD1). This segment is deleted from all
strains of BCG and the majority of environmental
mycobacteria
 Advantage : discriminate between MTb infection and
previous BCG vaccination.
 Polymerase chain reaction (PCR) – molecular tests for
detection of nucleic acid
 Single primer IS6110- Sn 47%, Sp 95%
 Multiplex PCR with multiple primer IS6110, 16SrRNA and dev RNA –
Sn 87 for ITB, 76 % for peritoneal TB
 NAAT :
 Assays amplify M. tuberculosis specific nucleic acid sequences using
a nucleic acid probe
 Requires as little as 10 bacilli from given sample
 Specificity 98-99%
 Major limitation : no drug susceptibility info
 Types:
 AMPICLOR MTB assay
 Amplified Mtb direct (AMTD2) assay
 LCx MTB assay, ABBOTT LCx probe system
 BD Probe Tec energy transfer (ET) system (DTB)
 INNO-LiPA RIF TB assay
 16S rRNA gene sequence analysis
 ASCITIC FLUID
 Exudate with protein level >2.5 gm/dl
 SAAG <1.1 (Low SAAG ascites)
 Sp gravity > 1.016
 Glucose < 30 mg
 Decreased pH
 LDH >90units/litre
 Lymphocyte predominant cells with count 250/cumm
 AFB in ascitic fluid is seen in only < 3% cases
 ADA in ascitic fluid >33 units/ml : 95% specificity, 98%
sensitivity
SENSITIVITY OF INVESTIGATIONS
INTESTINAL TB PERITONEAL TB
CASEATING
GRANULOMA
21% (15-40%) -
GRANULOMA 30-82%
AFB POSITIVITY 6-20% 2.9%
AFB CULTURE 6-54% 34.7%
TB PCR 47% (20-87%) 48-75%
GENE XPERT 8% 18-19%
ASCITIC FLUID ADA - 94%
LAPAROSCOPIC
VISUALISATION
- 92-93%
COMPLICATIONS
 Obstruction 20%
 Malabsorption, blind loop syndrome
 Dissemination of tuberculosis to other area of
abdomen as well as extra-abdominal sites
 Faecal fistula
 Cold abscess formation
 Hemorrhage, perforation (rare)
MANAGEMENT
 MEDICAL
 First line of management
 ATT
 SURGICAL
 Refractory cases
 Presenting as acute abdomen
TREATMENT
UPDATES IN PROTOCOL
 Daily regimen instead of thrice weekly doses
 Fixed drug combination
 Inroduction of Weight bands
 Ethambutol continued in continuation phase
 No extension of IP
 New categories:
 Drug sensitive
 Drug resistant
MEDICAL MANAGEMENT
DRUG DOSAGE (mg/Kg)
DAILY
ADVERSE EFFECTS
ISONIAZID 5 Peripheral Neuritis
Hepatitis
Rashes, Acne
RIFAMPICIN 10 Hepatitis
Orange urine
Skin rashes, Purpura
Flu syndrome
ETHAMBUTOL 15 Optic neuritis
Hyperuricemia
PYRAZINAMIDE 25 Hepatotoxicity
Hyperuricemia
Arthralgia, rashes
STREPTOMYCIN 15 Ototoxicity
Nephrotoxicity
DRUGS FOR DRUG SENSITIVE TB
REGIMEN FOR DRUG SENSITIVE
TUBERCULOSIS
Type of TB case Treatment regimen
in IP
Treatment regimen
in CP
New and previously
diagnosed DS TB
(2) HRZE (4) HRE
DAILY DOSE SCHEDULE FOR ADULTS AS PER
WEIGHT BANDS
Weight Category Number of tablets (FDC)
IP
HRZE
(75/150/400/275)
CP
HRE
(75/150/275)
25-34 Kg 2 2
35-49 Kg 3 3
50-64 Kg 4 4
65-75 Kg 5 5
>75 Kg 6 6
DRUGS FOR DRUG RESISTANT TUBERCULOSIS
A. Fluoroquinolones
 Levofloxacin
 Moxifloxacin
 Gatifloxacin
B. Second line injectables:
 Amikacin
 Kanamycin
 Streptomycin
C. Other second line agents:
 Ethionamide
 Cycloserine
 Linezolid
 Clofazimine
D. Add on agents(Not part of
Core MDR regimen):
 D1:
 Pyrazinamide
 Ethambutol
 High dose Isoniazid
 D2:
 Bedaquiline
 Delamanid
 D3:
 P-aminosalicylic acid
 Meropenem
 Amoxicillin-clavulanate
 Thioacetazone
TYPES OF DRUG RESISTANCES
 H Mono/Poly drug resistances:
 Isoniazid resistance
 Isoniazide + one of the first line drug except Rifampicin
 MDR:
 Isoniazid + Rifampicin resistant
 XDR:
 Isoniazid + Rifampicin + 2nd line injectable +
Fluoroquinolones
 RR:
 Rifampicin resistant
REGIMEN FOR DRUG RESISTANT TB
Regimen class IP CP
H mono/Poly DR TB (6) Lfx R E Z
MDR/
RR TB
Shorter regimen (9-11) (4-6)
Mfxh
Km/Am
Eto
Cfz
Z
Hh
E
(5)
Mfxh
Cfz
Z
E
Longer regimen (18-20) Bdq(6)
(18-20) Lfx
Lzd#
Cfz
#Lzd dose reduced to 300mg/day after 6 months
MODIFIED REGIMEN IN
HEPATOTOXICITY
INDICATIONS FOR STEROIDS:
 Miliary TB
 TB meningitis
 TB pericarditis
 Pleural and endobronchial TB
 Abdominal TB to prevent adhesions
 TB of mesenteric LN (rapidly progressive)
 Adrenal TB
 Genitourinary TB
 Ocular TB
SURGICAL MANAGEMENT
 Indications:
 Intestinal Obstruction
 Severe hemorrhage
 Acute abdominal presentation due to perforation
 Intra abdominal abscess/ fistula formation
 Uncertain diagnosis
 Differentiation from Crohn’s disease:
 Male, bloody stools
 Perianal disease
 Extraintestinal manifestations
 Linear ulcers, cobblestoning
 Mucosal bridging and involvement of rectum
SURGICAL MANAGEMENT
1. Ileocaecal resection with 5 cm margin
SURGICAL MANAGEMENT
2. Stricturoplasty:
 Single – stricturoplasty / RA (if bowel wall
is oedematous and friable)
 Multiple - strictures resection of ileum
and anastomosis is done (ideal). /
Multiple stricturoplasty (If Multiple
strictures with long segment gaps
between each).
 Resection is better option for stricture
within 10 cm of ileocaecal valve.
SURGICAL MANAGEMENT
 If perforation: resection & anastomosis done
 In severly contaminated peritoneum, resection and
exteriorisation is done. Bowel continuity is restored after
proper antitubercular therapy and proper nutritional
improvement.
 During therapy if patient develops ileocaecal
obstruction, ileotransverse colon anastomosis
(bypass) can be done
 Adhesive obstruction may be released through
laparoscopic adhesiolysis
 Drainage of intra-abdominal abscess, perianal
abscess and treatment for tuberculous fistula-in-
ano is done when necessary.
SURGICAL MANAGEMENT
 Management of acute type of peritoneal
tuberculosis:
 Exploratory laparotomy – reveals straw colored fluid
with tubercles in the pritoneum, greater omentum and
bowel wall
 Fluid is evacuated and collected for AFB study and
culture
 Omental biopsy is taken
 Abdomen is closed (without a drain) with tension
sutures to prevent burst abdomen and ATD is started.
SURGICAL MANAGEMENT
 Loculated form of peritoneal tuberculosis:
 Fluid aspiration under laparoscopic vision
 Purulent form of peritoneal tuberculosis:
 ATD
 Exploration of umbilicus, exploration of fistula and bowel
bypass.
 Prognosis poor
 Ano recto sigmoidal tuberculosis:
 ATD
 Fistulectomy
 Often sigmoid resection
RARE FORMS OF ABDOMINAL
TUBERCULOSIS
TB OESOPHAGUS
 Mimics Oesophageal CA
 Mid esophageal ulcer, dysphagia and
odynophagia, low grade fever
 Pathology - extension from nearby tubercular
LN into esophagus
 Barium swallow:
 Patient with mediastinal lymphadenopathies that
produced a fistula demonstrated by endoscopy
 Extensive esophageal ulceration
 Extrinsic compression due to lymphadenopathies
TB GASTRODUODENUM
 0.3-2.3% of patients with pulmonary TB
 Uncommon due to :
 Acidic environment
 Rapid gastric emptying
 Paucity of Peyer’s patches
 Gatric TB – may mimic Peptic ulcer not relieving to
antisecretory therapy , Gastric CA or sarcoidosis,
syphilis stomach
 Present as ulcerative, granulomatous or fibrosing
lesion – may result in GOO
 Duodenal TB – obstruction due to extrinsic
compression by LN
 Other presentations:
 Perforation
 Fistula
 Ulcer excavation into pancreas
 Obstructive jaundice due to CBD compression
 ATD should be initiated in all patients- curative in
most, especially ulcerative lesions
 Surgical intervention is required if GOO persists
despite medical management
 Surgical approach – partial gastric resection such
as Bilroth gastrectomy or a sleeve resection
JEJUNAL TB
 Presents with
 Single or multiple strictures
 Intestinal obstruction
 Perforation (proximal to stricture)
SEGMENTAL COLONIC TB
 Involvement of colon without ileocaecal region
 Involves sigmoid, ascending and transverse colon
 Pain and hematochezia is common
APPENDICEAL TB
 0.1 – 3% of patients with tuberculosis
 Isolated TB of appendix is rare
 Treatment of choice: Appendectomy followed by
ATD
TUBERCULOSIS OF SOLID ABDOMINAL ORGANS
 LIVER
 Exceedingly rare these days
 Usually diagnosed accidentally
during exploration
 Typical lesions are
granulomas, with or without
central caseating necrosis,
calcified masses and biliary
strictures
 TB peritoneal LN may cause obstructive jaundice
due to compression of bile duct
 Usually have hepatomegaly, with or without
jaundice
 Liver enzymes, particularly ALP, are elevated
 D/D: other conditions associated with hepatic
granulomas such as leprosy, Hodgkin disease,
brucellosis, infectious mononucleosis, IBD, syphilis
 Treatment : Chemotherapy
 Note: most ATT are hepatotoxic (except
ethambutol), hence close observation necessary
 SPLEEN
 Rare
 May present as splenic
abscess or hypersplenism
 Presence of multiple
hypoechoic lesion on USG
in a HIV patient is highly
suggestive of disseminated
TB
 Diagnosis is usually made
following surgical resecion
of the diseased spleen
 Pancreas:
 Like or part of miliary TB
 Common in immunocompromised
 Usually present as acute or chronic pancreatitis
 Pancreatic mass or abscess may develop
 Can mimic malignancy
 Treatment : ATD
TB & HIV
Estimates of TB HIV burden in India ( Global TB report 2021)
HIV positive TB incidence 53000, 3.8%
HIV positive TB mortality 11000, 0.78/lac
 People with HIV are 29 times more likely to develop TB
 Anti TB regimen and duration is same irrespective of HIV
status
 ATT should be started first
 ART must be offered to all patients with HIV & TB,
irrespective of CD4 count
 ART should be started as soon as TB treatment is
tolerated ( between 2 weeks to 2 months)
TB & HIV
 Preferred regimen of fixed dose combination:
 Tenofovir 300mg
 Lamivudine 300 mg
 Doltegravir 50 mg
 Avoid Nevirapine based regimen due to drug interaction
 Immune reconstitution inflammatory syndrome (IRIS) can
occur after ART initiation and requires appropriate
management
 Co-trimoxazole prophylaxis has to be ensured to prevent
opportunistic infections
 Counselling:
 Nature and course of both diseases
 Long term treatment and side effects
 Cough hygiene
 Screening of family members
 Safe sexual practices
 Abstain from alcohol, smoking & substance abuse
TB & PREGNANCY
 Diagnostic challenge due to common non-specific
symptoms
 May lead to:
 Repeated reproductive failures
 Fetal ill health
 Preterm delivery
 TB of the newborn and infants
 High maternal and perinatal morbidity and mortality
 NTEP and Maternal Health division aims towards
prevention, screening as a part of ANC for early
diagnosis and prompt management
TB & PREGNANCY
 1st trimester – standard regimen for Drug sensitive
TB
 Drug resistant TB – avoid pregnancy
 If patient becomes pregnant while on treatment:
<20 weeks <20 weeks
Advised MTP
MTP
Continue Treatment
Unwilling for MTP
Modified regimen
<12 weeks
Omit Km, Eto
Add PAS
>12 weeks
Omit Km only,
Add PAS
Modified regimen
Omit Km, add PAS till delivery
Replace PAS with Km after delivery
and continue till end of IP
FOLLOW UP & PROGNOSIS...
 Regular weight check to see for gain;
 Improvement in appetite;
 Reduction of abdominal pain and distension;
 Absence of fever;
 Normal bowel habits;
 Normal haemoglobin;
 ESR becoming normal;
 US abdomen shows improvement in sonological
features.
 Patients who are not responding in 6 weeks
should be reassessed again for—drug resistance;
associated other diseases like malignancy
(carcinomas or lymphoma), Crohn‘s disease,
eosinophilic enteritis.
 During therapy patient who is responding for drug
therapy can also go for intestinal obstruction due
to fibrosis during healing stage. It needs surgical
intervention.
CHALLENGES
 Abdominal TB is a great mimicker
: can mimic infections,
malignancy etc
 Can involve single abdominal
organ without pulmonary
involvement, only 15-25% has
concomitant pulmonary TB
 Correct clinical diagnosis in only
50%
 Diagnostic challenge due to non
specific presentation and delay
leads to complication
 Hence, HIGH INDEX OF
SUSPICION required for early
diagnosis
TAKE HOME
MESSAGE…
 Repeated surgery in abdominal
tuberculosis is difficult and dangerous as
chances of developing faecal fistula,
further adhesions are more likely.
 So timely diagnosis, proper
treatment and counselling
to patients is important…
REFERNCES
1. Oxford Textbook of Surgery, 2nd ed
2. Harrison’s Principles of Internal Medicine, 19th ed
3. Bailey & Love’s Short Practice of Surgery, 27th ed
ABDOMINAL TB-1.pptx

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ABDOMINAL TB-1.pptx

  • 2. SCOPE OF PRESENTATION  DEFINITION  HISTORY  AGENT  EPIDEMIOLOGY  ROUTES OF TRANSMISSION & PATHOGENESIS  CLASSIFICATION  INVESTIGATIONS  MANAGEMENT  RARE TYPES OF GI TUBERCULOSIS  TB IN HIV & PREGNANCY
  • 3. DEFINITION The term abdominal tuberculosis refers to tuberculous infection of the gastrointestinal tract, mesenteric lymph nodes, peritoneum and omentum, and of solid organs related to the gastrointestinal tract such as the liver, spleen and pancreas.
  • 4. HISTORY  Tuberculosis was first recognised in Fourth century BC  Hippocrates described a condition resembling tuberculosis in a patient with pulmonary lesions and intestinal disease  Charles Dickens (1812-70) described TB as: “Dreaded disease in which there is a gradual and quiet struggle between soul and body where mortal part whithers away grain by grain and get wasted”  Major cause of intestinal strictures and bowel obstruction in the 19th century and early part of 20th century
  • 5. HISTORY  1882 – Identification of the causative organism, Mycobaccterium tuberculosis, by Robert Koch  Formulated Koch’s postulates to describe the etiology of Cholera and TB  1998 – complete genetic sequence of M. tuberculosis was identified.
  • 6. AGENT  Mycobacterium tuberculosis (90%)  M. bovis (largely eliminated)  The tubercle bacilli is :  Gram positive  Aerobic  Non-motile  Non- spore bearing  Identified by Ziehl- Neelson acid fast differential staining method (high content of mycolic acid in cell wall)  Culture of organism is in Lowenstein-Jensen medium : 04-06 weeks
  • 7. Lowenstein Jensen media showing growth of Mycobacterium tuberculosis
  • 8. EPIDEMIOLOGY  GLOBAL INCIDENECE:  Among top 10 causes of death globally  2021 – 6.4 million people developed tuberculosis  In 2020 – estimated 1.6 million deaths incl 187,000 with HIV  1/4th of global population has latent TB infection  Complicated by emergence of MDR  India has 26 per cent of World TB cases  In 2021, TB incidence in India in all forms was 1,933,381 – 19% higher than 2020.  TB declared as notifiable disease by Govt of India on 09 May 2012  World TB day : 24 March
  • 9. EPIDEMIOLOGY  Common in India & developing countries, more frequently in people of poor socio-economic background  6th most common type of extrapulmonary TB following LN, pleura, GU tract, bones/joints and meninges .  Higher incidence in HIV infected patients : 36% of AIDS patient develop TB, among which 50 % develop abdominal TB
  • 11. EPIDEMIOLOGY Developed countries  Immigrant population  Ageing population  Increase in HIV Developing countries  Incomplete treatment  MDR strains  Increase in HIV/AIDS RE-EMERGENCE
  • 12. TRANSMISSION  Ingestion of contaminated food : causing primary abdominal tuberculosis  Swallowed sputum : containing tuberculous bacteria from primary pulmonary focus causing secondary abdominal tuberculosis.  Hematogenous spread: during bateremic phase that may follow primary TB  Lymphatic spread : from infected nodes (5-10%)  Direct spread :  From Fallopian tubes by retrograde spread to involve peritoneum (10%)  From adjacent organs  Disseminated in bile : since they are sequestrated and excreted from granulomas in liver
  • 14. PATHOGENESIS Bacilli enters GI mucosa Inflammatory reactions Bacilli carried to Peyer’s patches by phagocytes Tubercle formation Submucosal tubercles enlarge & undergo necrosis Endarteritis & edema Sloughing & ulceration Collagen accumulation Thickening & stenosis Penetration of serosa Tubercles on serosal surface Bacilli reaches lymphatics •Bowel & mesenteric lymphatic obstruction •Thick, fixed mass • Regional LN • Hyperlasia • Caseation necrosis • Calcification
  • 15. TYPES OF ABDOMINAL TUBERCULOSIS
  • 16. TYPES 1. Intestinal:  Ileocaecal region:  Ulcerative (60 %)  Hyperplastic  Ulcero-hyperplastic  Ileal region: commonly stricture type 2. Peritoneal  Acute  Chronic:  Ascitic type  Encysted (loculated) type  Plastic (fibrous/adhesive)  Purulent type 3. TB of mesentery and its LN 4. Ano-recto-sigmoidal 5. Involvement of organs: Liver, spleen and other forms of miliary TB 6. TB of omentum 7.Rare types:  Oesophageal  Gastroduodenal  Retroperitoneal TB
  • 17. ILEOCAECAL TUBERCULOSIS  Most common site of abdominal TB  Due to:  Stasis : bacterial contact time is more  Abundant Peyer’s patches  Minimal digestive activity  Fluid and electrolyte absorption  Types:  Ulcerative 60%  Hyperplastic  Ulcero-hyperplastic 30%
  • 18. ILEOCAECAL TUBERCULOSIS  Ulcerative  Common in old, malnourished people  Circumferential transverse ulcers – with skip lesions  Long standing ulcers cause fibrosis and later stricture formation (Napkin- ring structure)  Bowel adhesions are common  Mainly presents with diarrhoea, blood in stool, loss of appetite and reduced weight.
  • 19. Fig - Ileocaecal Tuberculosis: Note the sites and tubercles in ileocaecal valve
  • 20. Fig - Histology of ileocaecal tuberculosis showing Epithelioid cell granuloma with caseation
  • 22.  Hyperplastic:  10% common, less virulent  young, well nourished individual  Fibroblast reaction in submucosa and subserosa - thickening of bowel wall and LN enlargement, leading to nodular mass  Common in caecal part ILEOCAECAL TUBERCULOSIS Note the ileocaecal tuberculosis with stricture.
  • 23. ILEOCAECAL TUBERCULOSIS •Causes extensive chronic inflammation, fibrosis, bowel adhesions, nodal enlargement, often presents with mass in RIF •When presents as a mass- SAIO
  • 24.  Virulent organism  Poor body resistance, old people  Multiple transverse ulcers  Clinically -diarrhea, bleeding P/R, loss of appetite and reduced weight  Complications: stricture, Intestinal obstruction  Barium study - ileal strictures  Less virulent organism  Good body resistance, young individuals  Chronic granulomatous lesion in ileocaecal region  Presents as mass in RIF  Complications: SAIO  Barium study -pulled up caecum, obtuse ileocaecal angle ULCERATIVE HYPERPLASTIC ILEOCAECAL TUBERCULOSIS
  • 25.  Usually stricture type  May be multiple  Presents usually with intestinal obstruction, bowel adhesions, localisation, fibrosis  Perforation (5%) ILEAL TUBERCULOSIS
  • 26.  Pathology:  Enormous thickening of the parietal peritoneum with multiple tiny yellowish tubercles  Dense adhesions in peritoneum and omentum with content inside as small bowel looking like Abdominal cocoon (sclerosing encapsulating peritonitis). PERITONEAL TUBERCULOSIS
  • 27. ACUTE PRESENTATION  Mimics acute abdomen  On- table diagnosis  Presents with features of peritonitis  Due to perforation or rupture of mesenteric tubercular LN PERITONEAL TUBERCULOSIS
  • 28.  Photo A-C intraop findigns slide 24 Fig A to C - On-table findings in intestinal tuberculosis, of extensive involvement with multiple tiny tubercles, thickening, adhesions and involvement of mesenteric lymph nodes.
  • 29. CHRONIC PRESENTATION 1. Ascitic form (Wet type):  Distension of abdomen with dilated veins.  Ascitic tap reveals straw colored fluid from which AFB can be isolated. PERITONEAL TUBERCULOSIS
  • 30. 2. Encysted (Loculated) ascites:  Ascites gets loculated because of the fibrinous deposition  Dullness, which is not shifting, is the typical feature  May present as intra-abdominal mass, which may mimic ovarian cyst, retroperitoneal cyst or mesenteric cyst PERITONEAL TUBERCULOSIS
  • 31. 3. Plastic type (Dry type):  Widespread adhesions  Present with colicky abdominal pain, diarrhoea, wasting and loss of weight, doughy abdomen  D/D: Peritoneal carcinomatosis PERITONEAL TUBERCULOSIS
  • 32. 4. Purulent form:  Invariably due to tuberculous salpingitis  Presents as mass in the lower abdomen containing pus.  Cold abscess gets adherent to abdominal wall, umbilicus and may form an umbilical fistula  Patient commonly has got genitourinary tuberculosis PERITONEAL TUBERCULOSIS
  • 33. TUBERCULOUS MESENTERIC LYMPHADENITIS  Infection is usually through the Peyer’s patches  Commonly, right sided LN involved  Presents with general symptoms, pain in umbilical region and RIF, mass in RIF or features of acute appendicitis  Often coils of intestine get adherent to the caseated mesenteric LN leading to intestinal obstruction.  Caseating material may collect between the layers of the mesentery, forming a cold abscess – pseudomesenteric cyst.
  • 34.  Massive enlargement of mesenteric LN due to TB is called as Tabes mesenterica Fig - Note the location of mesenteric tuberculous lymphadenitis in the right iliac fossa. But it can occur anywhere in the line of mesentery. TUBERCULOUS MESENTERIC LYMPHADENITIS
  • 35. Fig A-C: On table finding of Mesenteric tubercular lymphadenitis
  • 36. ABDOMINAL TUBERCULOSIS  Differential diagnosis:  CA caecum  Lymphoma  Retroperitoneal tumor  Non specific lymphadenitis
  • 37. ANO-RECTO-SIGMOIDAL TUBERCULOSIS  It mimics Carcinoma rectum, most common symptom - hematochezia  Presents as tenesmus, diarrhoea, discharge from fistula and ocassionally as mass per abdomen  Fistulas- painful and characteristically not indurated  TB fistulas -multiple, shallow, bluish in color with undermined edges.
  • 38. TUBERCULOSIS OF OMENTUM  Usually occurs as a part of the other types  Characteristic finding - Rolled up omentum with thickening  Often cold abscess can develop.
  • 39. DIFFERENT CLINICAL PRESENTATIONS OF ABDOMINAL TUBERCULOSIS  Clinical presentation:  Acute  Acute on chronic  Chronic  Common in 25-50 yrs age group, equal in both sexes  Constitutional symptoms:  Anemia, loss of weight & appetite (80%)  Diarrhoea (10-20%)  Fever (50-70%)  Failure to thrive, in children  Overall observed in 30% of the patients
  • 40. CLINICAL PRESENTATIONS  Abdominal Pain  Mass in RIF – may mimic Carcinoma caecum  Other sites of lump:  Central abdomen – enlarged mesenteric LN  Ilioinguinal – Iliopsoas abscess secondary to TB spine  Upper abdomen – rolled up omentum  Lower abdomen – Tubo-ovarian mass  Anywhere in abdomen – colonic TB, loculated ascites, matted bowel loops  Can be associated with adenocarcinoma of caecum or large bowel lymphoma or HIV
  • 41. SUMMARY OF SYMPTOMS AS PER TYPES Types Symptoms Ulcerative Diarrhoea and malabsorption Stricture Subacute or acute intestinal obstruction Hyperplastic Mass abdomen (RIF) and obstruction Ascites Generalised distension of abdomen Localised Intra abdominal mass, may mimic ovarian cyst, retroperitoneal or mesenteric cyst Peritoneal Abdominal cocoon, vague abdominal pain Mesenteric Tabes mesenterica, obstruction, mass  Atypical presentation:  Lower GI bleed  Fistula in ano  PID like pain  Gastric disease symptoms, Dysphagia  GI fistula
  • 43. INVESTIGATIONS  Hematological & Biochemical:  Anemia  Raised ESR, CRP  Hypoalbuminemia  Mantoux test  ELISA IgG
  • 44. INVESTIGATIONS  Chest X-Ray: to rule out primary focus
  • 45.  Straight X-Ray abdomen:  Intestinal obstruction  Calcified LN  Hollow viscus perforation
  • 46. BARIUM MEAL STUDY  Barium study X-Ray (Enteroclysis followed by barium enema or barium meal follow through) Series of a barium meal and follow-through showing strictures in the ileum, with the caecum pulled up into a subhepatic position and obtuse ileocecal angle.
  • 48.
  • 49.
  • 50. String sign – persistent narrow stream
  • 51.  Napkin lesions – ulcers & strictures in the terminal ileum and caecum  Earliest signs – increased transit time, hypersegmentation (chicken intestine), flocculation of barium  Mega ileum – multiple strictures with enormous dilatation of proximal ileum Chicken Intestine sign
  • 52. INVESTIGATIONS  USG findings:  Thickened bowel wall, mesentery, omentum, peritoneum  Loculated ascites with fine septae  Interloop ascites with alternate echogenic and echo free areas – Club sandwich appearance Club Sandwich appearance
  • 53. USG FINDINGS  Bowel loop radiates from its mesenteric root – Stellate sign  Mesenteric loop thickness more than 15 mm  Hepatosplenomegaly  LN enlargment, matted  Pulled up caecum presenting as a mass in subhepatic region – Pseudokidney sign (also seen in intususception)  Concentric uniform mural thickening
  • 54.  CT abdomen:  Very useful and reliable  Findings:  Thickened bowel wall, peritoneum  Ileocecal valve thickening  Enlarged/necrosed/ matted mesenteric nodes, often with cold abscess  Adhesions  Mesenteric thickening and nodules  Nodules in peritoneum/ solid organs  Adhesions in the bowel/ stricture/ obstructive features  Loculated ascites  CT guided FNAC / biopsy/ fluid aspiration INVESTIGATIONS
  • 55.
  • 56. COLONOSCOPY  To rule out CA  Shows mucosal nodules, ulcers, strictures, deformed ileocecal valve, mucosal oedema and diffuse colitis  Biopsy can be taken to establish diagnosis  Capsule endoscopy : useful to see small intestinal pathology in difficult cases due to obstruction at stricture site.
  • 57.  Laparoscopy :  Aids in visualisation  To collect ascitic fluid for analysis  To take biopsy  Blind percutaneous needle peritoneal biopsy  Using Cope’s / Abraham’s needle  Ascitic tap for fluid analysis  BACTEC MGIT broth culture INVESTIGATIONS
  • 58. NEWER SEROLOGICAL INVESTIGATIONS  IFN gamma release assay (IGRA) : based on detection of IFN gamma released by sensitied T cells on stimulation with specific Ags.  T spot TB test – directly count the no. of IFN gamma secreting T cells  Quantiferon TB Gold in-tube test – measures the concentration of IFN gamma secretion  Early secretory Antigen Target-6 (ESAT-6) & Culture filtrate protein-10 (CFP 10):  Both derived from a very specific region of MTb, the region of difference 1 (RD1). This segment is deleted from all strains of BCG and the majority of environmental mycobacteria  Advantage : discriminate between MTb infection and previous BCG vaccination.
  • 59.  Polymerase chain reaction (PCR) – molecular tests for detection of nucleic acid  Single primer IS6110- Sn 47%, Sp 95%  Multiplex PCR with multiple primer IS6110, 16SrRNA and dev RNA – Sn 87 for ITB, 76 % for peritoneal TB  NAAT :  Assays amplify M. tuberculosis specific nucleic acid sequences using a nucleic acid probe  Requires as little as 10 bacilli from given sample  Specificity 98-99%  Major limitation : no drug susceptibility info  Types:  AMPICLOR MTB assay  Amplified Mtb direct (AMTD2) assay  LCx MTB assay, ABBOTT LCx probe system  BD Probe Tec energy transfer (ET) system (DTB)  INNO-LiPA RIF TB assay  16S rRNA gene sequence analysis
  • 60.  ASCITIC FLUID  Exudate with protein level >2.5 gm/dl  SAAG <1.1 (Low SAAG ascites)  Sp gravity > 1.016  Glucose < 30 mg  Decreased pH  LDH >90units/litre  Lymphocyte predominant cells with count 250/cumm  AFB in ascitic fluid is seen in only < 3% cases  ADA in ascitic fluid >33 units/ml : 95% specificity, 98% sensitivity
  • 61. SENSITIVITY OF INVESTIGATIONS INTESTINAL TB PERITONEAL TB CASEATING GRANULOMA 21% (15-40%) - GRANULOMA 30-82% AFB POSITIVITY 6-20% 2.9% AFB CULTURE 6-54% 34.7% TB PCR 47% (20-87%) 48-75% GENE XPERT 8% 18-19% ASCITIC FLUID ADA - 94% LAPAROSCOPIC VISUALISATION - 92-93%
  • 62.
  • 63. COMPLICATIONS  Obstruction 20%  Malabsorption, blind loop syndrome  Dissemination of tuberculosis to other area of abdomen as well as extra-abdominal sites  Faecal fistula  Cold abscess formation  Hemorrhage, perforation (rare)
  • 65.  MEDICAL  First line of management  ATT  SURGICAL  Refractory cases  Presenting as acute abdomen TREATMENT
  • 66. UPDATES IN PROTOCOL  Daily regimen instead of thrice weekly doses  Fixed drug combination  Inroduction of Weight bands  Ethambutol continued in continuation phase  No extension of IP  New categories:  Drug sensitive  Drug resistant
  • 67. MEDICAL MANAGEMENT DRUG DOSAGE (mg/Kg) DAILY ADVERSE EFFECTS ISONIAZID 5 Peripheral Neuritis Hepatitis Rashes, Acne RIFAMPICIN 10 Hepatitis Orange urine Skin rashes, Purpura Flu syndrome ETHAMBUTOL 15 Optic neuritis Hyperuricemia PYRAZINAMIDE 25 Hepatotoxicity Hyperuricemia Arthralgia, rashes STREPTOMYCIN 15 Ototoxicity Nephrotoxicity DRUGS FOR DRUG SENSITIVE TB
  • 68. REGIMEN FOR DRUG SENSITIVE TUBERCULOSIS Type of TB case Treatment regimen in IP Treatment regimen in CP New and previously diagnosed DS TB (2) HRZE (4) HRE
  • 69. DAILY DOSE SCHEDULE FOR ADULTS AS PER WEIGHT BANDS Weight Category Number of tablets (FDC) IP HRZE (75/150/400/275) CP HRE (75/150/275) 25-34 Kg 2 2 35-49 Kg 3 3 50-64 Kg 4 4 65-75 Kg 5 5 >75 Kg 6 6
  • 70. DRUGS FOR DRUG RESISTANT TUBERCULOSIS A. Fluoroquinolones  Levofloxacin  Moxifloxacin  Gatifloxacin B. Second line injectables:  Amikacin  Kanamycin  Streptomycin C. Other second line agents:  Ethionamide  Cycloserine  Linezolid  Clofazimine D. Add on agents(Not part of Core MDR regimen):  D1:  Pyrazinamide  Ethambutol  High dose Isoniazid  D2:  Bedaquiline  Delamanid  D3:  P-aminosalicylic acid  Meropenem  Amoxicillin-clavulanate  Thioacetazone
  • 71. TYPES OF DRUG RESISTANCES  H Mono/Poly drug resistances:  Isoniazid resistance  Isoniazide + one of the first line drug except Rifampicin  MDR:  Isoniazid + Rifampicin resistant  XDR:  Isoniazid + Rifampicin + 2nd line injectable + Fluoroquinolones  RR:  Rifampicin resistant
  • 72. REGIMEN FOR DRUG RESISTANT TB Regimen class IP CP H mono/Poly DR TB (6) Lfx R E Z MDR/ RR TB Shorter regimen (9-11) (4-6) Mfxh Km/Am Eto Cfz Z Hh E (5) Mfxh Cfz Z E Longer regimen (18-20) Bdq(6) (18-20) Lfx Lzd# Cfz #Lzd dose reduced to 300mg/day after 6 months
  • 74. INDICATIONS FOR STEROIDS:  Miliary TB  TB meningitis  TB pericarditis  Pleural and endobronchial TB  Abdominal TB to prevent adhesions  TB of mesenteric LN (rapidly progressive)  Adrenal TB  Genitourinary TB  Ocular TB
  • 75. SURGICAL MANAGEMENT  Indications:  Intestinal Obstruction  Severe hemorrhage  Acute abdominal presentation due to perforation  Intra abdominal abscess/ fistula formation  Uncertain diagnosis  Differentiation from Crohn’s disease:  Male, bloody stools  Perianal disease  Extraintestinal manifestations  Linear ulcers, cobblestoning  Mucosal bridging and involvement of rectum
  • 76. SURGICAL MANAGEMENT 1. Ileocaecal resection with 5 cm margin
  • 77. SURGICAL MANAGEMENT 2. Stricturoplasty:  Single – stricturoplasty / RA (if bowel wall is oedematous and friable)  Multiple - strictures resection of ileum and anastomosis is done (ideal). / Multiple stricturoplasty (If Multiple strictures with long segment gaps between each).  Resection is better option for stricture within 10 cm of ileocaecal valve.
  • 78. SURGICAL MANAGEMENT  If perforation: resection & anastomosis done  In severly contaminated peritoneum, resection and exteriorisation is done. Bowel continuity is restored after proper antitubercular therapy and proper nutritional improvement.  During therapy if patient develops ileocaecal obstruction, ileotransverse colon anastomosis (bypass) can be done  Adhesive obstruction may be released through laparoscopic adhesiolysis  Drainage of intra-abdominal abscess, perianal abscess and treatment for tuberculous fistula-in- ano is done when necessary.
  • 79. SURGICAL MANAGEMENT  Management of acute type of peritoneal tuberculosis:  Exploratory laparotomy – reveals straw colored fluid with tubercles in the pritoneum, greater omentum and bowel wall  Fluid is evacuated and collected for AFB study and culture  Omental biopsy is taken  Abdomen is closed (without a drain) with tension sutures to prevent burst abdomen and ATD is started.
  • 80. SURGICAL MANAGEMENT  Loculated form of peritoneal tuberculosis:  Fluid aspiration under laparoscopic vision  Purulent form of peritoneal tuberculosis:  ATD  Exploration of umbilicus, exploration of fistula and bowel bypass.  Prognosis poor  Ano recto sigmoidal tuberculosis:  ATD  Fistulectomy  Often sigmoid resection
  • 81. RARE FORMS OF ABDOMINAL TUBERCULOSIS
  • 82. TB OESOPHAGUS  Mimics Oesophageal CA  Mid esophageal ulcer, dysphagia and odynophagia, low grade fever  Pathology - extension from nearby tubercular LN into esophagus  Barium swallow:  Patient with mediastinal lymphadenopathies that produced a fistula demonstrated by endoscopy  Extensive esophageal ulceration  Extrinsic compression due to lymphadenopathies
  • 83. TB GASTRODUODENUM  0.3-2.3% of patients with pulmonary TB  Uncommon due to :  Acidic environment  Rapid gastric emptying  Paucity of Peyer’s patches  Gatric TB – may mimic Peptic ulcer not relieving to antisecretory therapy , Gastric CA or sarcoidosis, syphilis stomach  Present as ulcerative, granulomatous or fibrosing lesion – may result in GOO  Duodenal TB – obstruction due to extrinsic compression by LN
  • 84.  Other presentations:  Perforation  Fistula  Ulcer excavation into pancreas  Obstructive jaundice due to CBD compression  ATD should be initiated in all patients- curative in most, especially ulcerative lesions  Surgical intervention is required if GOO persists despite medical management  Surgical approach – partial gastric resection such as Bilroth gastrectomy or a sleeve resection
  • 85. JEJUNAL TB  Presents with  Single or multiple strictures  Intestinal obstruction  Perforation (proximal to stricture)
  • 86. SEGMENTAL COLONIC TB  Involvement of colon without ileocaecal region  Involves sigmoid, ascending and transverse colon  Pain and hematochezia is common
  • 87. APPENDICEAL TB  0.1 – 3% of patients with tuberculosis  Isolated TB of appendix is rare  Treatment of choice: Appendectomy followed by ATD
  • 88. TUBERCULOSIS OF SOLID ABDOMINAL ORGANS  LIVER  Exceedingly rare these days  Usually diagnosed accidentally during exploration  Typical lesions are granulomas, with or without central caseating necrosis, calcified masses and biliary strictures
  • 89.  TB peritoneal LN may cause obstructive jaundice due to compression of bile duct  Usually have hepatomegaly, with or without jaundice  Liver enzymes, particularly ALP, are elevated  D/D: other conditions associated with hepatic granulomas such as leprosy, Hodgkin disease, brucellosis, infectious mononucleosis, IBD, syphilis  Treatment : Chemotherapy  Note: most ATT are hepatotoxic (except ethambutol), hence close observation necessary
  • 90.  SPLEEN  Rare  May present as splenic abscess or hypersplenism  Presence of multiple hypoechoic lesion on USG in a HIV patient is highly suggestive of disseminated TB  Diagnosis is usually made following surgical resecion of the diseased spleen
  • 91.  Pancreas:  Like or part of miliary TB  Common in immunocompromised  Usually present as acute or chronic pancreatitis  Pancreatic mass or abscess may develop  Can mimic malignancy  Treatment : ATD
  • 92. TB & HIV Estimates of TB HIV burden in India ( Global TB report 2021) HIV positive TB incidence 53000, 3.8% HIV positive TB mortality 11000, 0.78/lac  People with HIV are 29 times more likely to develop TB  Anti TB regimen and duration is same irrespective of HIV status  ATT should be started first  ART must be offered to all patients with HIV & TB, irrespective of CD4 count  ART should be started as soon as TB treatment is tolerated ( between 2 weeks to 2 months)
  • 93. TB & HIV  Preferred regimen of fixed dose combination:  Tenofovir 300mg  Lamivudine 300 mg  Doltegravir 50 mg  Avoid Nevirapine based regimen due to drug interaction  Immune reconstitution inflammatory syndrome (IRIS) can occur after ART initiation and requires appropriate management  Co-trimoxazole prophylaxis has to be ensured to prevent opportunistic infections  Counselling:  Nature and course of both diseases  Long term treatment and side effects  Cough hygiene  Screening of family members  Safe sexual practices  Abstain from alcohol, smoking & substance abuse
  • 94. TB & PREGNANCY  Diagnostic challenge due to common non-specific symptoms  May lead to:  Repeated reproductive failures  Fetal ill health  Preterm delivery  TB of the newborn and infants  High maternal and perinatal morbidity and mortality  NTEP and Maternal Health division aims towards prevention, screening as a part of ANC for early diagnosis and prompt management
  • 95. TB & PREGNANCY  1st trimester – standard regimen for Drug sensitive TB  Drug resistant TB – avoid pregnancy  If patient becomes pregnant while on treatment: <20 weeks <20 weeks Advised MTP MTP Continue Treatment Unwilling for MTP Modified regimen <12 weeks Omit Km, Eto Add PAS >12 weeks Omit Km only, Add PAS Modified regimen Omit Km, add PAS till delivery Replace PAS with Km after delivery and continue till end of IP
  • 96. FOLLOW UP & PROGNOSIS...  Regular weight check to see for gain;  Improvement in appetite;  Reduction of abdominal pain and distension;  Absence of fever;  Normal bowel habits;  Normal haemoglobin;  ESR becoming normal;  US abdomen shows improvement in sonological features.  Patients who are not responding in 6 weeks should be reassessed again for—drug resistance; associated other diseases like malignancy (carcinomas or lymphoma), Crohn‘s disease, eosinophilic enteritis.  During therapy patient who is responding for drug therapy can also go for intestinal obstruction due to fibrosis during healing stage. It needs surgical intervention.
  • 97. CHALLENGES  Abdominal TB is a great mimicker : can mimic infections, malignancy etc  Can involve single abdominal organ without pulmonary involvement, only 15-25% has concomitant pulmonary TB  Correct clinical diagnosis in only 50%  Diagnostic challenge due to non specific presentation and delay leads to complication  Hence, HIGH INDEX OF SUSPICION required for early diagnosis
  • 98. TAKE HOME MESSAGE…  Repeated surgery in abdominal tuberculosis is difficult and dangerous as chances of developing faecal fistula, further adhesions are more likely.  So timely diagnosis, proper treatment and counselling to patients is important…
  • 99. REFERNCES 1. Oxford Textbook of Surgery, 2nd ed 2. Harrison’s Principles of Internal Medicine, 19th ed 3. Bailey & Love’s Short Practice of Surgery, 27th ed