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TB from Head to Toes
Presented by
*The increasing prevalence of
tuberculosis in both immunocompetent
and immunocompromised individuals
in recent years makes this disease a
topic of universal concern.
Introduction
*Because tuberculosis demonstrates
a variety of clinical and radiologic
findings and has a known propensity
for dissemination from its primary
site, it can mimic numerous other
disease entities..
Introduction
*The World Health Organization (WHO)
estimates that each year more than
8 million new cases of tuberculosis occur
and approximately 3 million persons die
from the disease.
*Ninety-five percent of tuberculosis cases
occur in developing countries.
*It is estimated that between 19 and 43% of
the world's population is infected with
Mycobacterium tuberculosis, the
bacterium that causes tuberculosis
infection and disease
Epidemiology
Epidemiology
 Most cases in the US are due to eactivation,
especially amongst immigrants
 Highest risk of progression to active TB is
within 2 years of seroconversion
 Increase in incidence in late 1980s-early 90s
largely due to HIV
 Needs to be reported to the health
department
Microbiology
 Aerobic
 Bacillus (rod-shaped)
 Non-spore forming
 Non-motile
 Cell wall – mycolic acid – retains acid fast
stain
 Growth - doubling time of 15-20 hrs.
 3-8 weeks for growth on solid media
TB Skin Testing
 PPD – purified protein derivative of
tuberculin (antigenic)
 Delayed type hypersensitivity reaction
 PPD may not become “positive” until 3
months after exposure
 Boosting effect
Skin Test Interpretation
 PPD >/= 5 mm:
– HIV patients
– Recent contacts of someone with TB
– Fibrotic changes on CXR c/w prior TB
– Organ transplant recipients
– Immunosuppressed (includes patients
receiving the equivalent of 15 mg/day or
more of prednisone for one month or
more)
Skin Test Interpretation
 PPD >/= 10 mm:
– Recent immigrants (< 5 years) from high
prevalence areas (Eastern Europe, Latin
America, Asia, Africa)
– IV drug users
– Residents and employees of high risk facilities
(hospitals, nursing homes, homeless shelters,
prisons)
– Children < 4 years of age
– Mycobacteriology lab personnel
Skin Test Interpretation
 PPD >/= 10 mm:
– People with medical conditions that place
them at high risk for active TB
 Chronic renal failure
 Diabetes mellitus
 Silicosis
 Leukemias/lymphomas
 Carcinoma of the head/neck or lung
 Weight loss > 10% of ideal body weight
 Gastrectomy/jejunoileal bypass
Skin Test Interpretation
 PPD >/= 15 mm:
– Low risk people
– Routine tuberculin testing not
recommended for low risk populations
Skin Test Intrepretation
 False positives:
– Non-tuberculous mycobacterial infection
– BCG vaccination
 False negatives:
– HIV
– Malnutrition
– Steroid therapy
– Recent infection
BCG
 Bacille Calmette-Guerin vaccination:
 Live attenuated mycobacterial strain derived
from M. bovis
 Can yield false positives to PPD – less likely
as time from vaccination increases
 Reactions > 20 mm likely are true
 CDC advises that the PPD be interpreted by
the same guidelines (ignore the BCG history)
Quantiferon Testing
 Whole blood in vitro test:
– Lymphocytes release IFN gamma in
presence of 2 TB antigens
 Will be positive in latent or active TB
 Advantages:
– No error in interpretation
– No follow-up in 48-72 hours
– No boosting
– Not affected by BCG
Quantiferon Testing
 Disadvantages:
– Must be processed within 12 hours of
collection
– False + with atypical mycobacteria
– Too many indeterminate results with
current version (Q-Gold)
– May be less reliable in pregnant women,
children, and immunocompromised
– Does not distinguish between active and
latent TB
Causative organism;
Mycobacterium tuberculosis COMPLEX
Stained with:
-Modified gram stain: gram positive.
-Carbolfuchsin stain: *Cold method(Kynon)
*Hot(Zeil-Neelson)
- Fluorescent dyes: rhodamine and
auramine stains.
Bacteriology
QUANTITATION SCALE FOR ACID-FAST BACILLUS
SMEARS ACCORDING TO STAIN USED
Carbolfuchsin (× 1,000)
Fluorochrome
(× 250)
Quantity Reported
No AFB/300 fields No AFB/30 fields No AFB seen
1-2 AFB/300 fields 1-2 AFB/30 fields Doubtful, repeat
test
1-9 AFB/100 fields 1-9 AFB/10 fields Rare (1+)
1-9 AFB/10 fields 1-9 AFB/field Few (2+)
1-9 AFB/field 10-90 AFB/field Moderate (3+)
> 9 AFB/field > 90 AFB/field Numerous (4+)
Zeil-Neelson Staining
Wire 0.01 ml of specimen 200mm2 slide
Oil immersion field 0.02mm
Slide=10000 field=0.01ml specimen
10,000 organism/slide=1 AFB/field=1000,000 organism/ml
1000 organism/slide=1 AFB/10 field=100,000 organism/ml
100 organism/slide=1 AFB/100field=10,000 organism/ml
QUANTITATION SCALE FOR ACID-FAST BACILLUS
SMEARS ACCORDING TO STAIN USED
Carbolfuchsin (× 1,000)
Fluorochrome
(× 250)
Quantity Reported
No AFB/300 fields No AFB/30 fields No AFB seen
1-2 AFB/300 fields 1-2 AFB/30 fields Doubtful, repeat
test
1-9 AFB/100 fields 1-9 AFB/10 fields Rare (1+)
1-9 AFB/10 fields 1-9 AFB/field Few (2+)
1-9 AFB/field 10-90 AFB/field Moderate (3+)
> 9 AFB/field > 90 AFB/field Numerous (4+)
Cultures:
- Lowenstein Jensen media: 6-8
weeks.
-Bactec media: 2-8days. Radiolabelled 14c
labelled palmitic acid
-Mycobacterial growth indicator tube:
Middbrook broth+o2 sensitive fluroscent sensor to
indicate growth& bacilli can be identified by Gen
Probe method at the same day of detection.
Diagnosis of Active TB
 Acid fast stain of sputum
 Sputum AFB culture (culture needed
for drug susceptibility)
 Radiographic imaging (CXR, CT)
 PCR/NAT
 Fluid Aspiration
 Tissue biopsy – higher yield than fluid
Primary pulmonary tuberculosis
Primary pulmonary TB typically
manifests radiologically as parenchymal
disease, lymphadenopathy, pleural
effusion, miliary disease, or lobar or
segmental atelectasis.
Consolidation in primary tuberculosis. Frontal chest radiograph
demonstrates consolidation in the right middle lobe (straight
arrow) with right hilar adenopathy (curved arrow).
Tuberculomas in primary
tuberculosis. Frontal X-ray
of the right lung
demonstrates well-defined
nodules(arrows), findings
that are consistent with
tuberculomas.
Pulmonary parenchymal changes and lymphadenopathy in primary
tuberculosis. Axial contrast material–enhanced computed
tomographic (CT) scan demonstrates a parenchymal lung cavity in
the lingula (solid white arrow) with enlarged necrotic subcarinal
lymph nodes (black arrows). There is accompanying collapse of
the left lower lobe (open arrow).
Mediastinal TB adenopathy.Axial contrast-enhanced CT
scan demonstrates multiple enlarged mediastinal lymph
nodes with centralareas of low attenuation and peripheral
enhancement (arrows).
Pleural effusion. Axial contrast-enhanced CT scan
demonstrates a large, right-sided pleural collection.The
enhancing parietal pleura is uniformly thickened (arrows).
Miliary tuberculosis. Frontal radiograph shows
fine, discrete nodular areas of increased opacity
bilaterally.
Miliary tuberculosis. High-resolution CT scan obtained with
lung windowing demonstrates numerous fine, discrete nodules
bilaterally in a random distribution
Postprimary Tuberculosis
Postprimary disease results from reactivation of a
previously dormant primary infection in 90% of cases;
in a minority of cases, it represents continuation of the
primary disease . Postprimary tuberculosis is almost
exclusively a disease of adolescence and adulthood.
Cavitary postprimary tuberculosis. (Frontal radiograph
demonstrates a thick-walled cavity with smooth inner
margins in the left upper lobe (arrow).
Axial contrast-enhanced CT scan obtained with mediastinal
windowing demonstrates an enlarged mediastinal lymph node
with a central area of low attenuation (arrow).
Axial CT scan obtained with lung windowing demonstrates ill-
defined cavities (black arrows) accompanied by endobronchial
spread in the right upper lobe (white arrow).
Fibroproliferative disease. Axial CT scan
demonstrates bilateral diffuse, coarse, linear, and nodular
areas of increased attenuation with cavitation (arrows).
Lung destruction in postprimary tuberculosis. Axial CT scan
demonstrates a fibrotic, shrunken left lung with
compensatory overexpansion of the right lung extending
across the midline. Bronchiectatic changes are
noted bilaterally (arrows).
Bronchiectasis in postprimary tuberculosis. Axial CT scan
demonstrates bronchiectasis in the left lung (arrows) with areas of
emphysema.
Fibroproliferative disease. Frontal chest radiograph shows
clumped nodular and linear areas of increased opacity in both
upper lobes and in the right middle lobe (white arrows). There
is accompanying volume loss in the right upper lobe as well as
overlying apical pleural thickening (black arrow).
Cavitary tuberculosis associated with aspergilloma. Frontalradiographshows a
cavity in the left upperlobe (black arrow) with a dependent area of soft-tissue
opacity(solidwhitearrow). The crescenticarea of hyperlucency(open arrow)
represents residual air in the cavity and is referred to as the air crescent sign.
Axial CT scan shows dependent soft-tissueaspergilloma(black arrow) within
the cavity (solidwhitearrow), along with the air crescent sign (open arrow).
Endobronchial spread of tuberculosis.
Axial CT scan shows severe changes of bronchiolar dilatation
and impaction. Bronchiolar wall thickening (straight arrows) and
mucoid impaction of contiguous branching bronchioles produce a tree-
in-bud appearance (curved arrows).
Tuberculous broncholithiasis. Chest radiograph demonstrates partial atelectasis
of the right upper lobe (straight arrow) with calcified hilar lymph nodes
bilaterally (curved arrows). Axial CT scan demonstrates erosion of the right
main bronchus (straight solid arrow) by a calcified hilar lymph node (curved
arrow). A calcified precarinal lymph node is also noted (open arrow). The
differential diagnosis for mediastinal lymph node calcification includes
histoplasmosis, silicosis,and treatedlymphoma.
Tuberculous bronchostenosis.
Axial CT scan demonstrates
narrowing of the right main
bronchus (arrow).
Tuberculous involvement of
the left sternoclavicular
joint. Oblique radiograph
demonstrates irregularity
of the medial end of the left
clavicle (black arrow)
with an associated soft-tissue
mass (white arrow).
Plombage in a patient with postprimary tuberculosis. Frontal chest
radiograph demonstrates typical right-sided Lucite ball plombage.
There is thinning and disorganization of the overlying ribs (straight
arrow). Air-fluid levels in the Lucite balls (curved arrows) suggest
bronchopleural fistulas.
Cardiac Tuberculosis
Although tuberculosis rarely involves the heart
pericardial involvement may occasionally be
seen with mediastinal and pulmonary
tuberculosis and is a cause of calcific
pericarditis (
Tuberculoma of the right atrium in a patient with miliary tuberculosis. Axial T2-weighted
magnetic resonance (MR) image demonstrates a hyperintense mass in the right atrium (straight
arrow). Note also the right pleural effusion (curved arrow). The mass proved to be a
tuberculoma at surgery. Tuberculous pericarditis in a patient with pleuropulmonary
tuberculosis. Axial CT scan demonstrates pericardial thickening (straight solid arrow).
Pulmonary tuberculomas (curved arrows) and a right pleural effusion (open arrow) are also
seen.
Skeletal Tuberculosis
Tuberculous Spondylitis (Pott Disease)
The spine is the most frequent site of osseous
involvement in tuberculosis , with the upper lumbar
and lower thoracic spine being involved most
frequently. More than one vertebra is typically
affected, and the vertebral body is more commonly
involved than the posterior elements. An anterior
predilection is seen in the vertebral body
Tuberculous spondylitis. Lateral radiograph demonstrates obliteration of the disk
space (straight arrow) with destruction of the adjacent end plates (curved arrow)
and anterior wedging. Subligamentous spread of spinal tuberculosis. Lateral
radiograph demonstrates erosion of the anterior margin of the vertebral body
(arrow) caused by an adjacent soft-tissue abscess.
Tuberculous spondylitis. Axial CT scan demonstrates lytic
destruction of the vertebral body (black arrow) with an
adjoining soft-tissue abscess (white arrow).
Iliopsoas abscess.Axial CT scan demonstrates
large, multiloculated iliopsoas abscesses
bilaterally (arrowheads). Note also the presacral
abscess (solid arrow) accompanied by erosion of
the anterior sacrum (open arrow).
Calcified psoas abscess. Axial CT scan
demonstrates bilateral tuberculous psoas
abscesses with peripheral calcification (arrows).
Extraspinal Tuberculous
Osteomyelitis
Tuberculous osteomyelitis is usually hematogenous
in origin and is most commonly seen in bones of
the extremities, including the smallbones of the
hands and feet. In long, tubular bones, tuberculosis
often involves the epiphyses.In children,
metaphyseal foci can involve the growth plate. This
feature differentiates tuberculosis from pyogenic
infection
Tuberculous osteomyelitis involving the skull. Axial contrast-
enhanced CT scan demonstrates a bilobed, peripherally
enhancing cold abscess centered along the right frontal bone
(arrow, arrowhead). Note the significant edema and the mass
effect on the underlying brain parenchyma. Axial CT scan
obtained with bone windowing demonstrates an ill-defined
lytic area of bone destruction (arrow).
Tuberculous spondylitis. Sagittal T2-weighted MR
image demonstrates areas of increased signal
intensity due to edema in vertebral bodies.
Accompanying disk narrowing (white arrow) and
extension of the disease into the spinal canal (black
arrow) are also seen.
Tuberculous osteomyelitis. Anteroposterior radiograph
demonstrates a lytic area of bone destruction (arrow) with
transphyseal spread of infection across the growth plate.
Tuberculous arthritis of the knee joint. Frontal radiograph
demonstrates periarticular osteopenia (black arrow), peripheral
osseous erosions (white arrow), and relative preservation of the
joint space. Tuberculous arthritis of the knee joint. Sagittal
gadolinium-enhanced T1-weighted MR image demonstrates
peripheral enhancement around the low-signal-intensity joint
collection (straight arrow). Note the presence of marginal joint
erosions (curved arrow).
Gastrointestinal Tuberculosis
Although abdominal tuberculosis is usually
secondary to pulmonary tuberculosis,
radiologic evaluation often shows no evidence
of lung disease
Ileocecum and Colon
The ileocecal region is the most common area of
involvement in the gastrointestinal tract due to
the abundance of lymphoid tissue. The natural
course of gastrointestinal tuberculosis may be
ulcerative, hypertrophic, or ulcerohypertrophic
Ileocecal tuberculosis.
Radiograph obtained
with peroral
pneumocolon technique
demonstrates a conical
and shrunken cecum
(straight arrow)
retracted out of the iliac
fossa by contraction of
the mesocolon. Note also
the narrowing of the
terminal ileum (curved
arrow).
Ileocecal tuberculosis. Axial CT scan demonstrates concentric cecal
wall thickening (arrow). Axial CT scan obtained caudad to a
demonstrates diffuse thickening of the terminal ileum (arrow).
Ileocecal tuberculosis and peritoneal tuberculosis (wet type). Axial
CT scan demonstrates concentric thickening of the cecum (straight
solid arrow). Small bowel dilatation (curved arrow), ascites in the
greater peritoneal space, and thickening of the peritoneum
(open arrow) are also seen.
Peritoneum
Peritoneal involvement in tuberculosis is rare and is
usually associated with widespread abdominal
disease involving lymph nodes or bowel .Three
principal types of tuberculous peritoneal
involvement are recognized. The wet type is the
most common and is associated with large amounts
of viscous ascitic fluid that may be either diffusely
distributed or loculated .The fluid demonstrates high
attenuation at CT due to its high protein and cellular
content .The dry or plastic type is uncommon and is
characterized by caseous nodules, fibrous peritoneal
reaction, and dense adhesions
The fibrotic fixed type (consists of large omental
masses, matted loops of bowel and mesentery,and,
on occasion, loculated ascites .CT may also
demonstrate tethering of bowel loops. Infiltration
of the mesentery, when associated with a large
amount of ascites, may have a stellate appearance
at CT.
Peritoneal tuberculosis (dry type). Axial CT scan
demonstrates thickening and infiltration of the
peritoneum (white arrows) along with thickening
of bowel loops. Note the small amount of loculated
fluid (black arrow).
Peritoneal tuberculosis (fibrotic type). Axial contrast-enhanced
CT scan demonstrates enhancing thickened peritoneum
(straight arrow) with an adjoining matted loop of small bowel
(curved arrow).
Abdominal tuberculous lymphadenitis.
Axial contrast-enhanced CT scan demonstrates multiple
enlarged mesenteric lymph nodes with central areas
of low attenuation (arrow).
Hepatic tuberculosis.
Axial contrast-enhanced
CT scan demonstrates multiple nonuniform,
low-attenuation lesions within the liver (straight arrows).
An enlarged gastrohepatic lymph node is also
seen (curved arrow).
Tuberculous
pyonephrosis.
Retrograde pyelogram
shows filling of the dilated
hydronephrotic lower and
middle pole of the right
kidney. The collecting
system has irregular
margins (straight solid
arrow) and shows
irregular filling defects
(curved arrow) from
necrosis of the
parenchyma. Upper pole
calcification is also seen
(open arrow).
Renal tuberculosis.
Chest radiograph that includes
the upper abdomen
demonstrates lobar
calcification in the right kidney
(black arrow). Note also the
bilateral fibrocalcific changes
in the upper lobes (white
arrows).
Renal tuberculosis
Axial contrast-enhanced
CT scan demonstrates left tuberculous pyonephrosis
(straight solid arrow) with extension of the inflammatory
process into the perinephric space (curved arrow)
and accompanying peritoneal disease (open arrow).
Adrenal tuberculosis.
Axial contrast-enhanced
CT scan demonstrates bilateral adrenal masses
with central low-attenuation areas (arrows).
Bladder tuberculosis.
Axial contrast-enhanced CT scan demonstrates a thickened and
deformed bladder with an enhancing wall (straight arrow). There is
extension of the inflammatory process to the anterior abdominal wall
(curved arrow). Intravenous urogram demonstrates a thickened,
contracted, low-capacity bladder (thimble bladder) (arrowhead) with
minimal dilatation of both ureters.
Endometrial tuberculosis.
Hysterosalpingogram demonstrates an obliterated
and deformed endometrial cavity (arrow)
due to tuberculous endometritis.
Cranial tuberculous meningitis.
Axial gadolinium-enhanced T1-weighted MR image demonstrates leptomeningeal
enhancement along the left sylvian fissure (straight arrow). There is an
accompanying ring-enhancing granuloma in the left parieto-occipital region
(curved arrow).
Cranial tuberculomas
Axial contrastenhanced CT scan demonstrates multiple
ring-enhancing lesions (straight arrows) along with
diffuse meningeal enhancement (curved arrow).
Solid caseating tuberculous granulomas involving the
cerebellum. Axial T2-weighted MR image demonstrates
multiple granulomas with central areas of hypointensity in
the cerebellum (arrows). Tuberculous granulomas involving
the cerebellum. Axial T1-weighted MR image demonstrates
isointense lesions with mildly hyperintense rims in the
cerebellum (arrows).
Bilateral tuberculous mastoiditis.
Highresolution CT scan of the temporal bone demonstrates
bilateral destructive lesions in the mastoid processes (straight
arrows). There is an accompanying cold abscess overlying
the right temporo-occipital region (curved arrow).
Orbital tuberculosis.
Axial contrast-enhanced CT scan demonstrates
an enhancing retinal lesion in the left orbit
(arrow).
Conclusions
Tuberculosis can affect virtually any organ system in the
body and can be devastating if left untreated. The
increasing prevalence of this disease in both
immunocompetent and immunocompromised individuals
makes tuberculosis a topic of universal concern.
Tuberculosis has a variety of radiologic appearances and
can mimic numerous other disease entities. A high degree
of clinical suspicion and familiarity with the various
radiologic manifestations of tuberculosis allow early
diagnosis and timely initiation of appropriate therapy,
thereby reducing patient morbidity.
TB from Head to Toes

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TB from Head to Toes

  • 1.
  • 2. TB from Head to Toes Presented by
  • 3.
  • 4. *The increasing prevalence of tuberculosis in both immunocompetent and immunocompromised individuals in recent years makes this disease a topic of universal concern. Introduction
  • 5. *Because tuberculosis demonstrates a variety of clinical and radiologic findings and has a known propensity for dissemination from its primary site, it can mimic numerous other disease entities.. Introduction
  • 6.
  • 7. *The World Health Organization (WHO) estimates that each year more than 8 million new cases of tuberculosis occur and approximately 3 million persons die from the disease. *Ninety-five percent of tuberculosis cases occur in developing countries. *It is estimated that between 19 and 43% of the world's population is infected with Mycobacterium tuberculosis, the bacterium that causes tuberculosis infection and disease Epidemiology
  • 8.
  • 9. Epidemiology  Most cases in the US are due to eactivation, especially amongst immigrants  Highest risk of progression to active TB is within 2 years of seroconversion  Increase in incidence in late 1980s-early 90s largely due to HIV  Needs to be reported to the health department
  • 10.
  • 11. Microbiology  Aerobic  Bacillus (rod-shaped)  Non-spore forming  Non-motile  Cell wall – mycolic acid – retains acid fast stain  Growth - doubling time of 15-20 hrs.  3-8 weeks for growth on solid media
  • 12. TB Skin Testing  PPD – purified protein derivative of tuberculin (antigenic)  Delayed type hypersensitivity reaction  PPD may not become “positive” until 3 months after exposure  Boosting effect
  • 13.
  • 14.
  • 15.
  • 16.
  • 17. Skin Test Interpretation  PPD >/= 5 mm: – HIV patients – Recent contacts of someone with TB – Fibrotic changes on CXR c/w prior TB – Organ transplant recipients – Immunosuppressed (includes patients receiving the equivalent of 15 mg/day or more of prednisone for one month or more)
  • 18. Skin Test Interpretation  PPD >/= 10 mm: – Recent immigrants (< 5 years) from high prevalence areas (Eastern Europe, Latin America, Asia, Africa) – IV drug users – Residents and employees of high risk facilities (hospitals, nursing homes, homeless shelters, prisons) – Children < 4 years of age – Mycobacteriology lab personnel
  • 19. Skin Test Interpretation  PPD >/= 10 mm: – People with medical conditions that place them at high risk for active TB  Chronic renal failure  Diabetes mellitus  Silicosis  Leukemias/lymphomas  Carcinoma of the head/neck or lung  Weight loss > 10% of ideal body weight  Gastrectomy/jejunoileal bypass
  • 20. Skin Test Interpretation  PPD >/= 15 mm: – Low risk people – Routine tuberculin testing not recommended for low risk populations
  • 21. Skin Test Intrepretation  False positives: – Non-tuberculous mycobacterial infection – BCG vaccination  False negatives: – HIV – Malnutrition – Steroid therapy – Recent infection
  • 22. BCG  Bacille Calmette-Guerin vaccination:  Live attenuated mycobacterial strain derived from M. bovis  Can yield false positives to PPD – less likely as time from vaccination increases  Reactions > 20 mm likely are true  CDC advises that the PPD be interpreted by the same guidelines (ignore the BCG history)
  • 23. Quantiferon Testing  Whole blood in vitro test: – Lymphocytes release IFN gamma in presence of 2 TB antigens  Will be positive in latent or active TB  Advantages: – No error in interpretation – No follow-up in 48-72 hours – No boosting – Not affected by BCG
  • 24. Quantiferon Testing  Disadvantages: – Must be processed within 12 hours of collection – False + with atypical mycobacteria – Too many indeterminate results with current version (Q-Gold) – May be less reliable in pregnant women, children, and immunocompromised – Does not distinguish between active and latent TB
  • 25. Causative organism; Mycobacterium tuberculosis COMPLEX Stained with: -Modified gram stain: gram positive. -Carbolfuchsin stain: *Cold method(Kynon) *Hot(Zeil-Neelson) - Fluorescent dyes: rhodamine and auramine stains. Bacteriology
  • 26. QUANTITATION SCALE FOR ACID-FAST BACILLUS SMEARS ACCORDING TO STAIN USED Carbolfuchsin (× 1,000) Fluorochrome (× 250) Quantity Reported No AFB/300 fields No AFB/30 fields No AFB seen 1-2 AFB/300 fields 1-2 AFB/30 fields Doubtful, repeat test 1-9 AFB/100 fields 1-9 AFB/10 fields Rare (1+) 1-9 AFB/10 fields 1-9 AFB/field Few (2+) 1-9 AFB/field 10-90 AFB/field Moderate (3+) > 9 AFB/field > 90 AFB/field Numerous (4+)
  • 27. Zeil-Neelson Staining Wire 0.01 ml of specimen 200mm2 slide Oil immersion field 0.02mm Slide=10000 field=0.01ml specimen 10,000 organism/slide=1 AFB/field=1000,000 organism/ml 1000 organism/slide=1 AFB/10 field=100,000 organism/ml 100 organism/slide=1 AFB/100field=10,000 organism/ml
  • 28. QUANTITATION SCALE FOR ACID-FAST BACILLUS SMEARS ACCORDING TO STAIN USED Carbolfuchsin (× 1,000) Fluorochrome (× 250) Quantity Reported No AFB/300 fields No AFB/30 fields No AFB seen 1-2 AFB/300 fields 1-2 AFB/30 fields Doubtful, repeat test 1-9 AFB/100 fields 1-9 AFB/10 fields Rare (1+) 1-9 AFB/10 fields 1-9 AFB/field Few (2+) 1-9 AFB/field 10-90 AFB/field Moderate (3+) > 9 AFB/field > 90 AFB/field Numerous (4+)
  • 29. Cultures: - Lowenstein Jensen media: 6-8 weeks. -Bactec media: 2-8days. Radiolabelled 14c labelled palmitic acid -Mycobacterial growth indicator tube: Middbrook broth+o2 sensitive fluroscent sensor to indicate growth& bacilli can be identified by Gen Probe method at the same day of detection.
  • 30. Diagnosis of Active TB  Acid fast stain of sputum  Sputum AFB culture (culture needed for drug susceptibility)  Radiographic imaging (CXR, CT)  PCR/NAT  Fluid Aspiration  Tissue biopsy – higher yield than fluid
  • 31.
  • 32.
  • 33.
  • 34.
  • 35. Primary pulmonary tuberculosis Primary pulmonary TB typically manifests radiologically as parenchymal disease, lymphadenopathy, pleural effusion, miliary disease, or lobar or segmental atelectasis.
  • 36. Consolidation in primary tuberculosis. Frontal chest radiograph demonstrates consolidation in the right middle lobe (straight arrow) with right hilar adenopathy (curved arrow).
  • 37. Tuberculomas in primary tuberculosis. Frontal X-ray of the right lung demonstrates well-defined nodules(arrows), findings that are consistent with tuberculomas.
  • 38. Pulmonary parenchymal changes and lymphadenopathy in primary tuberculosis. Axial contrast material–enhanced computed tomographic (CT) scan demonstrates a parenchymal lung cavity in the lingula (solid white arrow) with enlarged necrotic subcarinal lymph nodes (black arrows). There is accompanying collapse of the left lower lobe (open arrow).
  • 39. Mediastinal TB adenopathy.Axial contrast-enhanced CT scan demonstrates multiple enlarged mediastinal lymph nodes with centralareas of low attenuation and peripheral enhancement (arrows).
  • 40. Pleural effusion. Axial contrast-enhanced CT scan demonstrates a large, right-sided pleural collection.The enhancing parietal pleura is uniformly thickened (arrows).
  • 41. Miliary tuberculosis. Frontal radiograph shows fine, discrete nodular areas of increased opacity bilaterally.
  • 42. Miliary tuberculosis. High-resolution CT scan obtained with lung windowing demonstrates numerous fine, discrete nodules bilaterally in a random distribution
  • 43. Postprimary Tuberculosis Postprimary disease results from reactivation of a previously dormant primary infection in 90% of cases; in a minority of cases, it represents continuation of the primary disease . Postprimary tuberculosis is almost exclusively a disease of adolescence and adulthood.
  • 44. Cavitary postprimary tuberculosis. (Frontal radiograph demonstrates a thick-walled cavity with smooth inner margins in the left upper lobe (arrow).
  • 45. Axial contrast-enhanced CT scan obtained with mediastinal windowing demonstrates an enlarged mediastinal lymph node with a central area of low attenuation (arrow).
  • 46. Axial CT scan obtained with lung windowing demonstrates ill- defined cavities (black arrows) accompanied by endobronchial spread in the right upper lobe (white arrow).
  • 47. Fibroproliferative disease. Axial CT scan demonstrates bilateral diffuse, coarse, linear, and nodular areas of increased attenuation with cavitation (arrows).
  • 48. Lung destruction in postprimary tuberculosis. Axial CT scan demonstrates a fibrotic, shrunken left lung with compensatory overexpansion of the right lung extending across the midline. Bronchiectatic changes are noted bilaterally (arrows).
  • 49. Bronchiectasis in postprimary tuberculosis. Axial CT scan demonstrates bronchiectasis in the left lung (arrows) with areas of emphysema.
  • 50. Fibroproliferative disease. Frontal chest radiograph shows clumped nodular and linear areas of increased opacity in both upper lobes and in the right middle lobe (white arrows). There is accompanying volume loss in the right upper lobe as well as overlying apical pleural thickening (black arrow).
  • 51. Cavitary tuberculosis associated with aspergilloma. Frontalradiographshows a cavity in the left upperlobe (black arrow) with a dependent area of soft-tissue opacity(solidwhitearrow). The crescenticarea of hyperlucency(open arrow) represents residual air in the cavity and is referred to as the air crescent sign. Axial CT scan shows dependent soft-tissueaspergilloma(black arrow) within the cavity (solidwhitearrow), along with the air crescent sign (open arrow).
  • 52. Endobronchial spread of tuberculosis. Axial CT scan shows severe changes of bronchiolar dilatation and impaction. Bronchiolar wall thickening (straight arrows) and mucoid impaction of contiguous branching bronchioles produce a tree- in-bud appearance (curved arrows).
  • 53. Tuberculous broncholithiasis. Chest radiograph demonstrates partial atelectasis of the right upper lobe (straight arrow) with calcified hilar lymph nodes bilaterally (curved arrows). Axial CT scan demonstrates erosion of the right main bronchus (straight solid arrow) by a calcified hilar lymph node (curved arrow). A calcified precarinal lymph node is also noted (open arrow). The differential diagnosis for mediastinal lymph node calcification includes histoplasmosis, silicosis,and treatedlymphoma.
  • 54. Tuberculous bronchostenosis. Axial CT scan demonstrates narrowing of the right main bronchus (arrow).
  • 55. Tuberculous involvement of the left sternoclavicular joint. Oblique radiograph demonstrates irregularity of the medial end of the left clavicle (black arrow) with an associated soft-tissue mass (white arrow).
  • 56. Plombage in a patient with postprimary tuberculosis. Frontal chest radiograph demonstrates typical right-sided Lucite ball plombage. There is thinning and disorganization of the overlying ribs (straight arrow). Air-fluid levels in the Lucite balls (curved arrows) suggest bronchopleural fistulas.
  • 57. Cardiac Tuberculosis Although tuberculosis rarely involves the heart pericardial involvement may occasionally be seen with mediastinal and pulmonary tuberculosis and is a cause of calcific pericarditis (
  • 58. Tuberculoma of the right atrium in a patient with miliary tuberculosis. Axial T2-weighted magnetic resonance (MR) image demonstrates a hyperintense mass in the right atrium (straight arrow). Note also the right pleural effusion (curved arrow). The mass proved to be a tuberculoma at surgery. Tuberculous pericarditis in a patient with pleuropulmonary tuberculosis. Axial CT scan demonstrates pericardial thickening (straight solid arrow). Pulmonary tuberculomas (curved arrows) and a right pleural effusion (open arrow) are also seen.
  • 59. Skeletal Tuberculosis Tuberculous Spondylitis (Pott Disease) The spine is the most frequent site of osseous involvement in tuberculosis , with the upper lumbar and lower thoracic spine being involved most frequently. More than one vertebra is typically affected, and the vertebral body is more commonly involved than the posterior elements. An anterior predilection is seen in the vertebral body
  • 60. Tuberculous spondylitis. Lateral radiograph demonstrates obliteration of the disk space (straight arrow) with destruction of the adjacent end plates (curved arrow) and anterior wedging. Subligamentous spread of spinal tuberculosis. Lateral radiograph demonstrates erosion of the anterior margin of the vertebral body (arrow) caused by an adjacent soft-tissue abscess.
  • 61. Tuberculous spondylitis. Axial CT scan demonstrates lytic destruction of the vertebral body (black arrow) with an adjoining soft-tissue abscess (white arrow).
  • 62. Iliopsoas abscess.Axial CT scan demonstrates large, multiloculated iliopsoas abscesses bilaterally (arrowheads). Note also the presacral abscess (solid arrow) accompanied by erosion of the anterior sacrum (open arrow).
  • 63. Calcified psoas abscess. Axial CT scan demonstrates bilateral tuberculous psoas abscesses with peripheral calcification (arrows).
  • 64. Extraspinal Tuberculous Osteomyelitis Tuberculous osteomyelitis is usually hematogenous in origin and is most commonly seen in bones of the extremities, including the smallbones of the hands and feet. In long, tubular bones, tuberculosis often involves the epiphyses.In children, metaphyseal foci can involve the growth plate. This feature differentiates tuberculosis from pyogenic infection
  • 65. Tuberculous osteomyelitis involving the skull. Axial contrast- enhanced CT scan demonstrates a bilobed, peripherally enhancing cold abscess centered along the right frontal bone (arrow, arrowhead). Note the significant edema and the mass effect on the underlying brain parenchyma. Axial CT scan obtained with bone windowing demonstrates an ill-defined lytic area of bone destruction (arrow).
  • 66. Tuberculous spondylitis. Sagittal T2-weighted MR image demonstrates areas of increased signal intensity due to edema in vertebral bodies. Accompanying disk narrowing (white arrow) and extension of the disease into the spinal canal (black arrow) are also seen.
  • 67. Tuberculous osteomyelitis. Anteroposterior radiograph demonstrates a lytic area of bone destruction (arrow) with transphyseal spread of infection across the growth plate.
  • 68. Tuberculous arthritis of the knee joint. Frontal radiograph demonstrates periarticular osteopenia (black arrow), peripheral osseous erosions (white arrow), and relative preservation of the joint space. Tuberculous arthritis of the knee joint. Sagittal gadolinium-enhanced T1-weighted MR image demonstrates peripheral enhancement around the low-signal-intensity joint collection (straight arrow). Note the presence of marginal joint erosions (curved arrow).
  • 69. Gastrointestinal Tuberculosis Although abdominal tuberculosis is usually secondary to pulmonary tuberculosis, radiologic evaluation often shows no evidence of lung disease Ileocecum and Colon The ileocecal region is the most common area of involvement in the gastrointestinal tract due to the abundance of lymphoid tissue. The natural course of gastrointestinal tuberculosis may be ulcerative, hypertrophic, or ulcerohypertrophic
  • 70. Ileocecal tuberculosis. Radiograph obtained with peroral pneumocolon technique demonstrates a conical and shrunken cecum (straight arrow) retracted out of the iliac fossa by contraction of the mesocolon. Note also the narrowing of the terminal ileum (curved arrow).
  • 71. Ileocecal tuberculosis. Axial CT scan demonstrates concentric cecal wall thickening (arrow). Axial CT scan obtained caudad to a demonstrates diffuse thickening of the terminal ileum (arrow). Ileocecal tuberculosis and peritoneal tuberculosis (wet type). Axial CT scan demonstrates concentric thickening of the cecum (straight solid arrow). Small bowel dilatation (curved arrow), ascites in the greater peritoneal space, and thickening of the peritoneum (open arrow) are also seen.
  • 72. Peritoneum Peritoneal involvement in tuberculosis is rare and is usually associated with widespread abdominal disease involving lymph nodes or bowel .Three principal types of tuberculous peritoneal involvement are recognized. The wet type is the most common and is associated with large amounts of viscous ascitic fluid that may be either diffusely distributed or loculated .The fluid demonstrates high attenuation at CT due to its high protein and cellular content .The dry or plastic type is uncommon and is characterized by caseous nodules, fibrous peritoneal reaction, and dense adhesions
  • 73. The fibrotic fixed type (consists of large omental masses, matted loops of bowel and mesentery,and, on occasion, loculated ascites .CT may also demonstrate tethering of bowel loops. Infiltration of the mesentery, when associated with a large amount of ascites, may have a stellate appearance at CT.
  • 74. Peritoneal tuberculosis (dry type). Axial CT scan demonstrates thickening and infiltration of the peritoneum (white arrows) along with thickening of bowel loops. Note the small amount of loculated fluid (black arrow).
  • 75. Peritoneal tuberculosis (fibrotic type). Axial contrast-enhanced CT scan demonstrates enhancing thickened peritoneum (straight arrow) with an adjoining matted loop of small bowel (curved arrow).
  • 76. Abdominal tuberculous lymphadenitis. Axial contrast-enhanced CT scan demonstrates multiple enlarged mesenteric lymph nodes with central areas of low attenuation (arrow).
  • 77. Hepatic tuberculosis. Axial contrast-enhanced CT scan demonstrates multiple nonuniform, low-attenuation lesions within the liver (straight arrows). An enlarged gastrohepatic lymph node is also seen (curved arrow).
  • 78. Tuberculous pyonephrosis. Retrograde pyelogram shows filling of the dilated hydronephrotic lower and middle pole of the right kidney. The collecting system has irregular margins (straight solid arrow) and shows irregular filling defects (curved arrow) from necrosis of the parenchyma. Upper pole calcification is also seen (open arrow).
  • 79. Renal tuberculosis. Chest radiograph that includes the upper abdomen demonstrates lobar calcification in the right kidney (black arrow). Note also the bilateral fibrocalcific changes in the upper lobes (white arrows).
  • 80. Renal tuberculosis Axial contrast-enhanced CT scan demonstrates left tuberculous pyonephrosis (straight solid arrow) with extension of the inflammatory process into the perinephric space (curved arrow) and accompanying peritoneal disease (open arrow).
  • 81. Adrenal tuberculosis. Axial contrast-enhanced CT scan demonstrates bilateral adrenal masses with central low-attenuation areas (arrows).
  • 82. Bladder tuberculosis. Axial contrast-enhanced CT scan demonstrates a thickened and deformed bladder with an enhancing wall (straight arrow). There is extension of the inflammatory process to the anterior abdominal wall (curved arrow). Intravenous urogram demonstrates a thickened, contracted, low-capacity bladder (thimble bladder) (arrowhead) with minimal dilatation of both ureters.
  • 83. Endometrial tuberculosis. Hysterosalpingogram demonstrates an obliterated and deformed endometrial cavity (arrow) due to tuberculous endometritis.
  • 84. Cranial tuberculous meningitis. Axial gadolinium-enhanced T1-weighted MR image demonstrates leptomeningeal enhancement along the left sylvian fissure (straight arrow). There is an accompanying ring-enhancing granuloma in the left parieto-occipital region (curved arrow).
  • 85. Cranial tuberculomas Axial contrastenhanced CT scan demonstrates multiple ring-enhancing lesions (straight arrows) along with diffuse meningeal enhancement (curved arrow).
  • 86. Solid caseating tuberculous granulomas involving the cerebellum. Axial T2-weighted MR image demonstrates multiple granulomas with central areas of hypointensity in the cerebellum (arrows). Tuberculous granulomas involving the cerebellum. Axial T1-weighted MR image demonstrates isointense lesions with mildly hyperintense rims in the cerebellum (arrows).
  • 87. Bilateral tuberculous mastoiditis. Highresolution CT scan of the temporal bone demonstrates bilateral destructive lesions in the mastoid processes (straight arrows). There is an accompanying cold abscess overlying the right temporo-occipital region (curved arrow).
  • 88. Orbital tuberculosis. Axial contrast-enhanced CT scan demonstrates an enhancing retinal lesion in the left orbit (arrow).
  • 89. Conclusions Tuberculosis can affect virtually any organ system in the body and can be devastating if left untreated. The increasing prevalence of this disease in both immunocompetent and immunocompromised individuals makes tuberculosis a topic of universal concern. Tuberculosis has a variety of radiologic appearances and can mimic numerous other disease entities. A high degree of clinical suspicion and familiarity with the various radiologic manifestations of tuberculosis allow early diagnosis and timely initiation of appropriate therapy, thereby reducing patient morbidity.