Pulmonary Pathology Flashcards

1
Q

Describe the gross anatomy of the lung

A

Normal Lung (images):

- Gross photograph of normal lungs and heart

- Pleural surface is smooth and shiny

- Lungs extend down to the apex of the heart

- Cut surface of normal lung


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2
Q

Describe the anatomy of the trachea

A
  • Connects upper respiratory tract to lungs via bronchial tree

  • 15-20 C-shaped incomplete cartilage rings

    • Hyaline cartilage

  • Posterior wall fibrous tissue

  • Ciliated pseudostratified columnar epithelium
    
- Goblet cells (mucus producing)

  • Smooth muscle
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3
Q

Describe the anatomy of the bronchi

A
  • Ciliated pseudostratified columnar epithelium
    
- Goblet cells (mucus producing)

  • Smooth muscle

  • Hyaline cartilage
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4
Q

Describe the anatomy of the bronchioles

A
  • Ciliated simple columnar and cuboidal epithelium

  • Club cells

  • Smooth muscle

  • Elastic fibres
    
- <1mm in diameter
    
- Cartilage disappears at size <0.6mm

  • Terminal bronchioles supported by smooth muscle cells
  • Distal to each terminal bronchiole is acinus
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5
Q

Describe the anatomy of the alveoli

A
  • Respiratory zone starts at respiratory bronchiole -> consist of millions of alveoli


Alveoli consist of
 Type I and type II cells

- Type I pneumocytes (squamous epithelium) (95%)

- Type II pneumocytes (cuboidal epithelium, surfactant producing – protects alveoli from collapse during expiration)


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6
Q

Describe the anatomy of oxygen exchange

A
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7
Q

What are the five major groups of lung disease?

A

Obstructive Lung Diseases
:
- Chronic bronchitis

- Emphysema

- Asthma

Restrictive Lung Diseases:

- Acute Respiratory Distress Syndrome 

- Silicosis

Infective Lung Diseases
:
- Pneumococcal lung infection

- Tuberculosis

Vascular Lung Diseases

Neoplastic Lung Diseases

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8
Q

Describe obstructive lung disease

A
  • Increase in resistance to airflow due to partial or complete obstruction of the airways
  • Airway obstruction is worse with expiration -> decreased expiratory flow rate -> more force is required to expire a given volume of air, or emptying of lungs is slowed
  • FEV1 to FVC ratio is characteristically decreased -> FEV1/FVC is ≤ 70% in adults and < 85% in children
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9
Q

Describe restrictive lung disease

A
  • Refer to intrinsic lung diseases that are restrictive (limited potential of lungto expand)
  • Exclude other processes which limit lung expansion:

    • Chest wall abnormalities

    • Neuromuscular disease
      
- Large abdominal masses
  • Lung function test shows reduced compliance, reduced TLC, FVC and FEV1
  • Patients develop symptoms of progressive breathlessness and cough
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10
Q

What is the difference between obstructive and restrictive lung diseases?

A
  • Obstructive lung disease makes it hard to exhale all the air in the lungs.
  • People with restrictive lung disease have difficulty fully expanding their lungs with air

Differences in spirometry

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11
Q

What are the main characteristics and anatomy/histology of chronic bronchitis (Obstructive lung disease)?

A
  • Clinical definition: cough with sputum production ≥ 3 months in at least 2 consecutive years
    
- Aetiology: cigarette smoking


Types: 

1)Simple chronic bronchitis:

- productive cough (no airflow obstruction)

2) Chronic asthmatic bronchitis:

- cough, intermittent bronchospasm and wheezing
 3) Chronic obstructive bronchitis:

- cough and outflow obstruction


Pathogenesis

1.Hypertrophy of submucosal mucus glands (trachea and main bronchi) 

2.Hyperplasia of mucin-secreting goblet cells (smaller bronchi and bronchioles) 
=> Hypersecretion of mucus -> mucous plugging & overproduction of sputum

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12
Q

What are the main characteristics and anatomy/histology of emphysema (Obstructive lung disease)?

A
  • Damages and enlarges the alveoli in the lungs
    
- Most common cause is smoking, rarely congenital condition known as α1-antitrypsin deficiency

  • Dyspnea: Problems with exhalation -> shortness of breath and cough

Image: Both lungs are markedly enlarged; arrows indicate clusters of dilated air spaces which are conspicuous in the middle and lower lobes of the right lung and the lower lobe of the left lung

  1. Permanent dilation of air spaces distal to terminal bronchioles

  2. Destruction of alveolar walls -> loss of elastic
    recoil -> obstruction

    - Asymptomatic until > 1/3 lung parenchyma is destroyed

    - Can affect airways before distal alveoli, airways distal to terminal bronchioles, distal acinus
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13
Q

What are the differences between chronic bronchitis and emphysema?

A
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14
Q

What are the main characteristics and anatomy/histology of asthma (Obstructive lung disease)?

A
  • A chronic inflammatory disorder of the airways
 -> hyper-reactive airways

  • Recurrent episodes of wheezing, breathlessness, chest tightness and cough caused by bronchospasm (reversible) 

  • Status asthmaticus: severe condition in which asthma attacks follow one another without pause (severe and prolonged symptom; rare) -> can be fatal
  • Extrinsic asthma - type I hypersensitivity reaction induced by an extrinsic allergen (producing too much IgE)
  • Intrinsic asthma - non-immunological e.g. ingestion of aspirin; pulmonary viral infections, cold, exercise and stress
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15
Q

What are the main characteristics and anatomy/histology of acute respiratory distress syndrome (ARDS) (restrictive lung disease)?

A
  • Not a specific disease
    
- Common causes: infection, burns, gas inhalation

  • ARDS is caused by protein-rich pulmonary
    edema -> causes severe hypoxemia and impaired carbon dioxide excretion
    
- Syndrome of acute respiratory failure -> Rapid onset of respiratory distress (dyspnoea, tachypnoea & distress)

  • Diffuse alveolar capillary & epithelial damage

  • Leakage of proteins and fibrin into
    alveoli -> hyaline membranes

  • Life-threatening condition that occurs when there is severe fluid buildup in both lungs
    
- Some alveoli fill with fluid, others collapse -> lungs can no longer fill properly with air and they become stiff

  • Can be fatal within a few days (or lung damage with fibrosis)
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16
Q

Describe the pathogenesis of ARDS?

A

Acute phase (first 1–6 days): 

- Sloughing of the bronchial and alveolar epithelial cells
 - Neutrophils

- Air space filled with protein rich edema fluid

- Lung injury caused primarily by neutrophil-dependent and platelet-dependent damage to the endothelial and epithelial barriers of the lung

- Resolution delayed due to injury to the lung epithelial barrier
- prevents removal of alveolar edema fluid

- deprives lung of adequate quantities of surfactant

Sub-Acute phase (next 7-14 days):

- Some of the edema has usually been reabsorbed
 - Evidence of attempts at repair with proliferation of alveolar epithelial type II cells

- May also be fibroblast infiltration and some collagen deposition


Chronic phase (after 14 days): 

- Resolution of the acute neutrophilic infiltrate

- More mononuclear cells and alveolar macrophages in the alveoli

- Often more fibrosis with ongoing evidence of alveolar epithelial repair


Outcome: In many patients, resolution without fibrosis and gradual resolution of the edema and acute inflammation

17
Q

What is infective lung disease and the different types?

A
  • Pneumonia
  • Can be caused by bacteria, virus, mycoplasma and fungus
  • Presentation: acute or chronic

Histological appearances:

- fibrinopurulent alveolar exudate in acute bacterial pneumonias 

- mononuclear interstitial infiltrates in viral pneumonias 
- granulomas & cavitation in chronic pneumonias


Community-acquired acute pneumonias
:
- Most commonly caused by the bacteria Streptococcus pneumoniae 

- May follow an upper respiratory tract viral infection

- Lung parenchyma filled with inflammatory
exudate -> fibrinosuppurative consolidation 

- Onset usually abrupt, high fever, shaking chills, chest pain, productive mucopurulent cough


2 main types of acute bacterial pneumonia:

- lobar pneumonia (lobar topography)

- bronchopneumonia (with lobular topography)


18
Q

Describe the anatomy and histology of lobar pneumonia (lobar topography) and the types of hepatisation

A
  • Acute exudative inflammation of an entire pulmonary lobe

  • Lobe enlargement

  • Loss of spongy appearance

  • Hepatization (conversion of tissue (as of the lungs in pneumonia) into a substance which resembles liver tissue and may become solidified) stops abruptly at the fissure

  • Red hepatization: Early exudate is full of bacteria, RBC, neutrophils, fibrin
    
- Grey hepatization: Later exudate contains macrophages, broken down RBC, debris


19
Q

Describe the anatomy and histology of bronchopnuemonia (lobular (plural) topography)

A
  • Affects one or more lobes

  • Suppurative peribronchiolar inflammation
- Multiple foci of condensation (1-3 cm diameter, white-yellowish, imprecisely circumscribed)















Histology:

- Multiple small foci of inflammation

- Extensive congestion and dilation of blood vessels and areas of poorly circumscribed consolidation

- Areas of inflammation are separated by areas of normal lung parenchyma

20
Q

What are the histological changes of lobar pneumonia during the different stages of the disease?

A
  1. Congestion: Alveolar lumen fills with serous exudate (rare leucocytes), bacteria
  2. Red Hepatisation: Exudate fills with erythrocytes (cause of red appearance) and leukocytes
  3. Gray Hepatisation: Red blood cells breakdown (causing loss of red appearance) and exudate fills with macrophages
  4. Resolution: exudate within the alveolar spaces drains
21
Q

Describe tuberculosis (TB)

A
  • A chronic pneumonia caused byMycobacterium tuberculosis
  • Presence of granulomatous inflammation
  • Centres of tubercular granulomas undergocaseous necrosis
  • Usually involves the lungs


Primary tuberculosis:

- Develops in a previously unexposed, and therefore unsensitized, person

- Mainly asymptomatic -> latent phase
- ~ 5% develop clinically significant disease -> progressive TB
Secondary tuberculosis:

- Reactivation of dormant primary lesions many decades after initial infection

- Secondary TB – may be asymptomatic or with “afternoon” fever & night sweat, malaise, anorexia & weight loss


22
Q

Describe the Ghon complex in tuberculosis

A
  • The Ghon complexis the pathognomonic macroscopical lesion of primary pulmonary tuberculosis after initial infection in children

    • The Ghon focus

    • Lymphadenitis
      
 - Lymphangitis


  • Ghon focus consist of a calcified focus of infection and an associated lymph node
23
Q

Describe miliary tuberculosis

A
  • ~5% progressive primary TB

  • Mycobacterium tuberculosis can enter circulation via pulmonary vein -> can infect other organs (liver, spleen etc.)

  • TB in organ ->cell-mediated immune response activated

  • Infected sites become surrounded by macrophages -> form granuloma (give the typical appearance of Miliary tuberculosis)
24
Q

What are the classes of lung cancers and their frequency?

A
  • Adenocarcinoma (25-40%)
  • Squamous Cell Carcinoma (24-40%)
  • Small Cell Carcinoma (20-25%)
  • Large Cell Carcinoma (10-15%)
25
Q

What is mesothelioma?

A

Cancer affecting the mesothelial cells which cover most internal organs