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ASPERGILLOSIS
BY-DR NITIN WADHWANI
ASPERGILLUS INFECTION
INTRODUCTION:
• Aspergillus infections of the lung are caused by Aspergillus fumigatus
which are ubiquitous fungi found throughout nature.
• Results in disease in susceptible hosts when inhaled.
• The pathogenesis of Aspergillus infection varies with quality and
virulence of the inhaled organism and the status of the host defence
mechanisms.
• Characterised by spectrum of pathology related to an immune
response of individual to the organism.
ETIOLOGY:
IMMUNE
SYSTEM
MILD
IMMUNOCOMPR
OMISED
HYPERSENSITIVITY NORMAL
SEVERELY
IMMUNOCOMPR
OMISED
• ABPA • MYCETOMA SEMIINVASIVE
/CHRONIC
NECROTIZING
ASPERGILLOSIS
INVASIVE
PULMONARY
ASPERGILLOSIS
• MYCETOMA:
• Is non invasive colonization of preexisting cavity in immunologically normal
pt with cavitatory disease
• Mycetoma is a ball of coalscent mycelial hhyphae that typically colonize pre-
existing cavity.
• Clinical features :
1. Cough and expectoration
2. Hemoptysis-frequently seen in almost ½ of cases
Bleeding is usually due to friction between fungal ball and hypervascular wall
which releases endotoxins from fungus and causes type-3 reaction in cavity
wall.
• LOCATION :
• UPPER LOBES
• SUPERIOR SEGMENT OF LOWER LOBE
• TB
• SARCOIDOSIS
• BRONCHIECTASIS
• LUNG ABSCESS
• NF-1
• EMPHYSEMATOUS BULLA
PREDISPOSED PT:
XRAY CT SCAN
Round to oval mass of soft tissue density
lying within preexisting cavity.
Taken in supine and prone position
Air crescent sign Mass within the cavity
Decubitus xray – to demonstrate mobility
of fungal ball
Air crescent sign
Thickening of cavity wall –s/o signs of
early aspergillus infection
Mobile intracavitatory mass is
characteristic of aspergilloma.
Irregular air spaces within
Fungal strands bridging the fungus ball
&cavity wall maybe seen.
IMAGING FINDINGS:
D/D OF FUNGAL BALL AND
AIR CRESCENT SIGN :
Infection
Cavitating
neoplasm
Trauma
• Hydatid cyst
• Tuberculoma
• Bacterial lung
abscess
• Bronchial
adenoma
• Cystic
hamartoma
Pulmonary
hematoma
• Allergic aspergillosis is a result of hypersensitivity reaction that produce ABPA or
less commonly extrinsic allergic pneumonitis or Loeffler syndrome.
• It is airway disease.
• Only seen in patients with asthma and cystic fibrosis.
• There is airway colonization -> complex hypersensitivity reaction (1 > III).
ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS:
C/F:
1. Cough
2. Wheezing
3. a/s allergic symptoms
• Eosinophil derived inflammation (fleeting infiltration).
• Plugging of bronchial wall with mucus plugs (contain septate hyphae)
• Th2 mediated inflammation (IL-5, 4,13) of bronchial wall
• cough with sputum (hyphae)
• Longterm- Irreversible dilatation
• Bronchiectasis.
Pathogenesis:
• Bronchiectasis – more in upper lobe , central, proximal airways and is B/L
• Mucus plugging with hyphae can also lead to atelectatsis.
• Adherence of conidia to respiratory epithelial cells
• cellular dysfunction
• Initially cilial disruption
• The fungal colony grows,hyphae are produced invade between & through epithelialcells
• Leading to substantial tissue disruption
Pathogenesis:
ABPA:
CHRONIC
ABPA:
ACUTE ABPA:
TYPE I REACTION :IMMEDIATE IgE
MEDIATED
TYPE III REACTION:DELAYED IMMUNE
COMPLEX IgA MEDIATED
• Pathology
• Allergic bronchopulmonary aspergillosis is the result of hypersensitivity
(esp fumigatus) .
• It grows within the lumen of the bronchi, without invasion.
• The hypersensitivity initially causes bronchospasm and bronchial wall
• Ultimately, there is bronchial wall damage with loss of muscle and bronchial
in bronchiectasis (typically central bronchiectasis) 7.
• Both types I and III allergic reactions have been implicated 4.
XRAY CT SCAN
Non segmental consolidation in upper
lobe
Bronchiectasis
Lobar collapse Mucoid impaction
Branching thick tubular opacity bronchial wall thickening: common
Pul cavitation cavitation: 10%
Hyperinflated lung fields
Gloved finger sign
Central bronchiectasis
ACUTE ABPA:
Gloved finger sign
:
CHRONIC ABPA:
IMAGING FEATURES:
• Bronchiectasis :
1. Bronchial wall thickening
2. Tramline shawdows
3. Ring formation
• Fibrosis: linear fibrotic band , can also cause traction bronchiectasis
• Loss of volume in upper lobe
A clinical staging system has been developed :
•stage I: acute
•stage II: remission
•stage III: recurrent exacerbation
•stage IV: steroid-dependent asthma
•stage V: pulmonary fibrosis
Major and minor criteria have also been established .
•major criteria
• clinical
• asthma (approximately 90% of patient may have asthma )
• radiographic features
• pulmonary opacities (transient or chronic)
• central bronchiectasis
• immune system
• blood eosinophilia
• immediate skin reactivity to Aspergillus antigen (elevated IgG and/or IgE against A.
fumigatus)
• increased serum IgE (>1000 IU/ml)
•minor criteria
• fungal elements in sputum
• expectoration of brown plugs/flecks
• delayed skin reactivity to fungal antigens
This form typically occurs in patients with a depressed immune system, but not as profoundly
immunocompromised as bone marrow patients who more frequently develop angioinvasive
aspergillosis. Patients are typically middle-aged. Risk factors, therefore, include 1-3:
•corticosteroids - most common systemic immunodepressant 3
•diabetes mellitus
•alcoholism
•chronic liver disease
•malnutrition
SEMI-INVASIVE(CHRONIC
NECROTIZING ASPERGILLOSIS)
IMAGING
FEATURES :
• AREA OF CONSOLIDATION IN UPPER LOBE
• PROGRESSES TO THICK WALLED CAVITY
• ADJACENT PLEURAL THICKENING .
• CONFINED TO IMMUNOCOMPROMISED HOST.
INVASIVE PULMONARY
ASPERGILLOSIS:
IMAGING FEATURES:
• MULTIPLE/ SINGLE ILLDEFINED OPACITIES
• DIFFUSE B/L CONSOLIDATION
• LARGE WEDGE SHAPED PLEURAL BASED LESION
• CAVITATION OF NODULE
• AIR CRESCENT SIGN
IMAGING FEATURES:
CT SCAN:
• 1-3 CM NODULES
• SEGMENTAL CONSOLIDATION
• CT HALO SIGN :ggo around the
nodules
Aspergillosis Imaging and Types

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Aspergillosis Imaging and Types

  • 2. ASPERGILLUS INFECTION INTRODUCTION: • Aspergillus infections of the lung are caused by Aspergillus fumigatus which are ubiquitous fungi found throughout nature. • Results in disease in susceptible hosts when inhaled. • The pathogenesis of Aspergillus infection varies with quality and virulence of the inhaled organism and the status of the host defence mechanisms. • Characterised by spectrum of pathology related to an immune response of individual to the organism.
  • 4. IMMUNE SYSTEM MILD IMMUNOCOMPR OMISED HYPERSENSITIVITY NORMAL SEVERELY IMMUNOCOMPR OMISED • ABPA • MYCETOMA SEMIINVASIVE /CHRONIC NECROTIZING ASPERGILLOSIS INVASIVE PULMONARY ASPERGILLOSIS
  • 5. • MYCETOMA: • Is non invasive colonization of preexisting cavity in immunologically normal pt with cavitatory disease • Mycetoma is a ball of coalscent mycelial hhyphae that typically colonize pre- existing cavity. • Clinical features : 1. Cough and expectoration 2. Hemoptysis-frequently seen in almost ½ of cases Bleeding is usually due to friction between fungal ball and hypervascular wall which releases endotoxins from fungus and causes type-3 reaction in cavity wall.
  • 6.
  • 7. • LOCATION : • UPPER LOBES • SUPERIOR SEGMENT OF LOWER LOBE
  • 8. • TB • SARCOIDOSIS • BRONCHIECTASIS • LUNG ABSCESS • NF-1 • EMPHYSEMATOUS BULLA PREDISPOSED PT:
  • 9. XRAY CT SCAN Round to oval mass of soft tissue density lying within preexisting cavity. Taken in supine and prone position Air crescent sign Mass within the cavity Decubitus xray – to demonstrate mobility of fungal ball Air crescent sign Thickening of cavity wall –s/o signs of early aspergillus infection Mobile intracavitatory mass is characteristic of aspergilloma. Irregular air spaces within Fungal strands bridging the fungus ball &cavity wall maybe seen. IMAGING FINDINGS:
  • 10.
  • 11.
  • 12. D/D OF FUNGAL BALL AND AIR CRESCENT SIGN : Infection Cavitating neoplasm Trauma • Hydatid cyst • Tuberculoma • Bacterial lung abscess • Bronchial adenoma • Cystic hamartoma Pulmonary hematoma
  • 13. • Allergic aspergillosis is a result of hypersensitivity reaction that produce ABPA or less commonly extrinsic allergic pneumonitis or Loeffler syndrome. • It is airway disease. • Only seen in patients with asthma and cystic fibrosis. • There is airway colonization -> complex hypersensitivity reaction (1 > III). ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS: C/F: 1. Cough 2. Wheezing 3. a/s allergic symptoms
  • 14. • Eosinophil derived inflammation (fleeting infiltration). • Plugging of bronchial wall with mucus plugs (contain septate hyphae) • Th2 mediated inflammation (IL-5, 4,13) of bronchial wall • cough with sputum (hyphae) • Longterm- Irreversible dilatation • Bronchiectasis. Pathogenesis:
  • 15. • Bronchiectasis – more in upper lobe , central, proximal airways and is B/L • Mucus plugging with hyphae can also lead to atelectatsis. • Adherence of conidia to respiratory epithelial cells • cellular dysfunction • Initially cilial disruption • The fungal colony grows,hyphae are produced invade between & through epithelialcells • Leading to substantial tissue disruption Pathogenesis:
  • 16. ABPA: CHRONIC ABPA: ACUTE ABPA: TYPE I REACTION :IMMEDIATE IgE MEDIATED TYPE III REACTION:DELAYED IMMUNE COMPLEX IgA MEDIATED
  • 17. • Pathology • Allergic bronchopulmonary aspergillosis is the result of hypersensitivity (esp fumigatus) . • It grows within the lumen of the bronchi, without invasion. • The hypersensitivity initially causes bronchospasm and bronchial wall • Ultimately, there is bronchial wall damage with loss of muscle and bronchial in bronchiectasis (typically central bronchiectasis) 7. • Both types I and III allergic reactions have been implicated 4.
  • 18. XRAY CT SCAN Non segmental consolidation in upper lobe Bronchiectasis Lobar collapse Mucoid impaction Branching thick tubular opacity bronchial wall thickening: common Pul cavitation cavitation: 10% Hyperinflated lung fields Gloved finger sign Central bronchiectasis ACUTE ABPA:
  • 19.
  • 21.
  • 22.
  • 23.
  • 24.
  • 25. CHRONIC ABPA: IMAGING FEATURES: • Bronchiectasis : 1. Bronchial wall thickening 2. Tramline shawdows 3. Ring formation • Fibrosis: linear fibrotic band , can also cause traction bronchiectasis • Loss of volume in upper lobe
  • 26. A clinical staging system has been developed : •stage I: acute •stage II: remission •stage III: recurrent exacerbation •stage IV: steroid-dependent asthma •stage V: pulmonary fibrosis Major and minor criteria have also been established . •major criteria • clinical • asthma (approximately 90% of patient may have asthma ) • radiographic features • pulmonary opacities (transient or chronic) • central bronchiectasis • immune system • blood eosinophilia • immediate skin reactivity to Aspergillus antigen (elevated IgG and/or IgE against A. fumigatus) • increased serum IgE (>1000 IU/ml) •minor criteria • fungal elements in sputum • expectoration of brown plugs/flecks • delayed skin reactivity to fungal antigens
  • 27. This form typically occurs in patients with a depressed immune system, but not as profoundly immunocompromised as bone marrow patients who more frequently develop angioinvasive aspergillosis. Patients are typically middle-aged. Risk factors, therefore, include 1-3: •corticosteroids - most common systemic immunodepressant 3 •diabetes mellitus •alcoholism •chronic liver disease •malnutrition SEMI-INVASIVE(CHRONIC NECROTIZING ASPERGILLOSIS)
  • 28. IMAGING FEATURES : • AREA OF CONSOLIDATION IN UPPER LOBE • PROGRESSES TO THICK WALLED CAVITY • ADJACENT PLEURAL THICKENING .
  • 29.
  • 30. • CONFINED TO IMMUNOCOMPROMISED HOST. INVASIVE PULMONARY ASPERGILLOSIS: IMAGING FEATURES: • MULTIPLE/ SINGLE ILLDEFINED OPACITIES • DIFFUSE B/L CONSOLIDATION • LARGE WEDGE SHAPED PLEURAL BASED LESION • CAVITATION OF NODULE • AIR CRESCENT SIGN
  • 31. IMAGING FEATURES: CT SCAN: • 1-3 CM NODULES • SEGMENTAL CONSOLIDATION • CT HALO SIGN :ggo around the nodules

Editor's Notes

  1. 2.Collection of cresentric air which seperates wall of cavity from inner mass
  2. Gravity dependent fungal ball in cavity
  3. Gloved finger sign:mucoid impaction seen typically as branching opacities u/s central,upper lobe distribution
  4. Gloved finger sign
  5. Chest x-ray demonstrates tubular branching opacities in the right upper lobe. In the left upper lobe a number of parallel lines extending from the hilum (tram track) suggest bronchiectasis. 
  6. CT reveals a branching lesion in the superior segment of the left lower lobe with classic finger in glove appearance which represents mucous filling dilated bronchi (i.e. bronchoceles).
  7. Bilateral upper lobar, right middle lobar and to less extent left lower lobar bronchiectasis with endobronchial hyperdense mucoid impaction giving the finger in glove appearance most evident in the right middle lobe with subsequent middle lobe collapse
  8. b/l central bronchiectasis with mucous filled bronchi