Tuberculosis Flashcards

1
Q

How long do TB Bacilli take to form a colony on a culture?

How is it spread?

After how many weeks of treatment does sputum infectivity become minimal?

A
  • 2-6 weeks
  • Infected droplets
  • 2 weeks (Can leave hospital after this time)
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2
Q

Describe the Pathogenesis of infection with Mycobacterium tuberculosis

A
  • Alveolar macrophages phagocytose MTB but are not able to kill them
  • The macrophages initiate cell-mediated immunity, which leads to emergence of Activated Macrophages which have enhanced ability to kill MTB. This takes 6 weeks to develop
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3
Q

How does Tuberculosis look histologically?

What cells may be seen?

A
  • Granuloma with central caseation (aka tubercles)
  • Lymphocytes
  • Epitheloid Histiocytes
  • Langhans giant cells
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4
Q

Primary TB occurs on first exposure to MTB.

What usually follows deposition of MTB in the alveoli?

A

Development of a Sub-Pleural focus of Tubercles called the Primary/ Ghon’s Focus, in any lung zone

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5
Q

Which lymph nodes do bacilli drain to from the Primary/ Gohn’s Focus?

What is the Primary Complex?

A

Hilar lymph nodes

The Primary Focus + the Hilar Lymph nodes

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6
Q

Most primary TB infections will heal with/ without calcification of the Primary Complex.

How can the bacilli spread before healing occurs?

A

Enters lymphatic drainage then venous drainage, spreading to other parts of the lung as well as to other organs

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7
Q

With cell-mediated immunity, the infection is contained and the primary complex heals, but some bacilli are still alive in lungs/ other organs.

What is this called?

What 2 tests can be used to characterise this?

A

Latent Tuberculosis

  • QuantiFERON test/ IGRA (Interferon Gamma Release Assay)
  • Tuberculin skin test
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8
Q

When does TB reactivation usually occur?

A

When immune mechanism are impaired/ fail

E.g old age, malnutrition, HIV, Immunosuppression

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9
Q

Describe the basis of the IGRA/ QuantiFERON test

A

Based on ability of MTB Antigens to stimulated host production of Interferon Gamma

  • Patient’s blood lymphocytes are cultured with MTB Antigens
  • If exposed to TB before, T lymphocytes produce Interferon Gamma
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10
Q

Why can the IGRA/ QuantiFERON test be used to distinguish Latent TB from previous BCG or Exposure to atypical mycobacteria?

A

Antigens used in test are not present in;

  • Atypical mycobacteria
  • Bacilli used in the TB vaccine (BCG)
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11
Q

Describe the Tuberculin skin test

A
  • Tuberculin is injected intra-dermally (a protein derived from mycobacteria)
  • Skin reaction 48-72hrs later indicates previous exposure to TB (Type IV Hypersensitivity)

(Immunity and hypersensitivity develop at the same time in a naturally infected person)

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12
Q

What percentage of people with TB have a risk of developing active disease?

A

10%

5% Primary, 5% Post-primary/ Latent reactivation

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13
Q

Where is Post-Primary Pulmonary TB most often seen?

List 5 conditions/ pathologies that can result from this

A

In the Upper Lung Zones
(Higher pAO2 may predispose to reactivation)

  • Cavity formation
  • Haemorrhage
  • Spread to rest of lung
  • Pleural effusion
  • Miliary TB
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14
Q

How can Post-Primary Pulmonary TB lead to Cavity formation?

A
  • Softening and liquefaction of the caseous material
  • Discharged into a Bronchus

(Fibrous tissue forms around these lesions but is unable to limit extension)

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15
Q

How can Post-Primary Pulmonary TB lead to Haemorrhage?

A
  • Exension of the caseous process into vessels in cavity walls
  • Causes Haemoptysis
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16
Q

How can Post-Primary Pulmonary TB spread to rest of the lung?

A

Caseous and liquified material spread through the bronchial tree

17
Q

How can Post-Primary Pulmonary TB lead to Pleural Effusion?

A

Seeding of bacilli in pleura or hypersensitivity

18
Q

How can Post-Primary Pulmonary TB lead to Miliary TB?

A
  • Rupture of a caseous focus into a blood vessel

- Dissemination of bacilli throughout body

19
Q

What is extrapulmonary TB?

A

Reactivation of latent TB in sites other than lungs

20
Q

TB symptoms have a gradual onset.

List 6 symptoms

A
  • Fatigue
  • Malaise
  • Fever
  • Weight loss
  • Sweats
  • Cough (Dry/Mucus/ Blood)
21
Q

How does TB appear on examination?

A
  • May be no signs
  • May hear Crackles
  • Possible signs of Cavitation, Fibrosis, Pleural Effusion if these are present
22
Q

What does CXR show in TB?

A

Pulmonary shadowing, may be;

  • Patchy solid lesions
  • Cavitated solid lesions
  • Streaky fibrosis flecks of calcification
23
Q

How can active TB be diagnosed?

A

Identfication of the Tubercle Bacillus (Smear, Culture etc)

24
Q

How is TB treated?

A

RIPE

  • Rifampicin, Isoniazid (INAH), Pyrazinamide and Ethambutol ALL for 2 months
  • Rifampicin and INAH for further 4 months
  • Pyrioxidine (B6) must be given with INAH to present peripheral nerve damage
25
Q

Can Tuberculin skin testing show a False Positive?

Can it show a false negative

A

Yes

False negative possible if Immunosuppressed

26
Q

List side effects of each of the drugs used to treat TB

A

Rifampicin;

  • Hepatitis
  • Red orange urine

Isoniazid/ INAH;

  • Heptitis
  • Peripheral neuropathy (so give Vit B6)

Pyrazinamide;
- Hepatitis

Ethambutol;
- Optic neuritis

27
Q

Can the IGRA/ QuantiFERON test distinguish Active disease from Latent infection?

A

No