Infection Flashcards

1
Q

Pneumonia

A

Community acquried pneumonia: not recently hospitalised or long term care facility >14 d

Hospital acquired pneumonia: >48 hours after admission or <48 hours after discharge

  • Segmental/subsegmental consolidation
  • Centrilobular nodules/GGO
  • +/- cavity
  • Pleural effusions/empyema
  • Lobe enlargement + buging fissures: Klebsiella
  • Pneumatoceles: S.Aureus
  • Cavitations: S.Aureus, gram-negative, anaerobes
  • Hyperinflation: viral pneumonia
  • Children: round pneumonia
  • Hilar lymphadenopathy: TB, mycoplasma, fungal

DDx:

  • Pulmonary oedema
  • ARDS
  • COP
  • Drug induced lung disease
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2
Q

Lung Abscess

A

Pathology:

  • Lung necrosis secondary to microbial infection: parenchymal destruction –> scarring –> bronchiectasis –> cyst formation
  • Consolidation progressed into cavity over 7-14d
  • Complications:
    • Empyema
    • Bronchopleural fistula –> hydropneumothorax
    • Pulmonary gangrene with necrotic lung fragments in abscess cavity (sequestrum), bronchopulmonary fistula
  • Eitiology:
    • Aspriation of polymicrobial bacteria from oral cavity
    • Primary lung infection: S.Aureus, Klebsiella, S.pyogenes, Type 3 pneumococcus, post transplant or immunosupressed
    • Septic emboli
    • Malignancy +/- secondary infection (post obstructive)
    • Miscellenaeous: direct trauma/neighboring organs/hematogenous seeding
  • Organisms:
    • Anaerobes (-50%)
      • peptostreptococcus
      • Bateriodes
      • Fusobacterium
      • Microaerophilic streptococci
    • Aerobes:
      • S.auerus
      • Klebsiella pneumoniae
      • Strep pyogenes
      • Hemophilius influenzae
      • Actinomyces
      • Nocardia
      • Mycobacterium: TB/MAC
    • Fungal:
      • Asperigillus
      • Cryptococus
      • Histoplasma
      • Blastomyces
      • Coccidiodes
    • Parasites: Paragonimus,entamoeba

Clinical:

  • Old
  • M>F (4:1)
  • High risk: poor entition, seizure disorder, alcoholism, smoker, immunocompromised

Progonosis:

  • 33% mortality if untreated
  • Heals with scarring, bronchiectasis and cystic change

Rx:

  • Antibiotics
  • Bronchoscopy if failed treatment –> assess for endobronchial lesion. (not in acude phase for abscesses as potential spillover of contents to normal lung)
  • Surgery
  • Percutaneous drainage (controversial)

Imaging: CXR/CT

  • Location: gravitationally dependent (as often linked to aspiration)
  • Irregular, thick-walled, spherical lung cavity with relatively smooth inner margin
    • May contain air-fluid level (50%), air, fluid
    • Acute angles with adjacent chest wall (unlike empyema)
  • +/- surroudning consolidation/GGO (50%)
  • +/- pleural effusions (50%) may develop into empyema (33%)
  • Bronchogenic spread –> multiple abscesses
  • Reactive hilar/mediastinal lymphadenopathy
  • Bronchopleural fistula: hydropneumothorax, empyema
  • Air-cresent: invasive aspergilosis/mycetoma
  • Lemierre disease: pharyngeal infection –> IJ thrombosis –> septic emboli (Fusobacterium)

DDx:

  • Pneumatocoele (especially in S.Auerus pneumonia)
  • TB: upper lobe consolidation wtih cavitation
  • Infected bulla
  • Lung Ca
  • Septic emboli
  • Inflammatory: Wegener, Necrobiotic nodules
  • Sequestration

https://app.radprimer.com/document/19251c2b-cb3e-454e-bceb-10812e8d5d70/lesson/d594f863-2508-4182-aa21-fbec747bd3cd

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3
Q

Septic Emboli

A

Pathology:

  • Infected embolic material seeding from extrapulmonary source
  • usually sharply demarcated from adjacent normal lung
  • Eitiology:
    • IVDU: Staph aureus
    • Infective endocarditis
    • Lemierre syndrome: fusobacterium
    • Infected lines/pacemakers
    • Burn patients: p.aeruginosa
    • Osteomyelitis
    • ICU on broadspectrum AB: fungal
    • IDC

Rx: broad spectrum AB, drainage of empyema, treat source of infection

Imaging (radiograph/CT):

  • Location: peripheral and basal predominance (blood pool)
  • Multiple descrete nodules
    • Cavitation: thick walled, usually lack air-fluid level
    • Halo sign: surrounding GGO (gram neg)
  • Air bronchograms: gram positive
  • Pulmonary infarct: subpleural wedge shaped consolidation
  • Feeding vessel sign: vessel leading directily to nodule/wedge-shaped opacity
  • +/- Mediastinal lymphadenopathy (20%)
  • No intravascular clots
  • Plerual effusions/empyema

DDx:

  • Pulmonary emboli
  • Pneumonia
  • Pulmonary mets

https://app.statdx.com/document/septic-emboli-pulmonary/53eb01f6-3812-4d44-93e5-78d9eaba680f?searchTerm=septic%20emboli

https://app.radprimer.com/document/53eb01f6-3812-4d44-93e5-78d9eaba680f/lesson/d594f863-2508-4182-aa21-fbec747bd3cd

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4
Q

Pneumococcal Pneumonia

A

Pathology:

  • Streptococcus pneumonia: gram positive, 2/3 of bacterial pneumonia
  • Colonize nasopharynx –> aerosol inhalation
  • Complications:
    • Empyema
    • ARDS
    • Meningitis
    • Sepsis

Imaging:

  • Lobar consolidation (most common)
    • Peripheral
    • Airbronchograms
    • Surrounding GGO
    • Centrilobular nodules/tree-in-bud/GGO in early stages
  • Can be round and mass like in children (round pneumonia)
  • Parapneumonic effusion (50%) –> look for empyema
  • Lymphadenopathy (50%)
  • Cavitation + abscess formation rare

DDx:

  • Other bacterial pneumonia
  • Viral pneumonia
  • Aspiration pneumonia/pneumonitis
  • Pulmonary hemorrhage
  • Cancer
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5
Q

Staphlococcus Pneumonia

A

Pathology:

  • Staphylococcus (usually s.aureus)
  • Community vs hospital acquried
  • MRSA common

Imaging:

  • Location: multifocal/bilateral
  • Patchy/lobar consolidation
  • Cavitation/Abscess formation –> heals to form pneumatocoele (may take months to years to resolve)
  • Parapneumonic pleural effusions (common) –> empyema
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6
Q

Klebsiella Pneumonia

A

Pathology:

  • Klebsiella pneumoniae: gram negative bacteria + clear capsule
  • High rate of abscess + empyema
  • High rate of bacteraemia
  • High mortality rate

Imaging:

  • Consolidation/GGO:
    • Lobar (can be multilobar)
    • voluminous inflammatory exudate
      • Bulging fissures (30%)
      • Expansion of consolidated lobes
      • Pulmonary necrosis
    • Sharp margins
    • RUL
  • Cavitation/abscess: common and occure early
  • Pulmonary gangrene: pulmonary vessel thrombosis
  • Pleural effusions + empyema
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7
Q

Nocardiosis

A

Pathology:

  • Nocardiosis Asteroides complex:
    • gram positive bacilli
    • weakly acid fast
    • Slow growth
    • PCR is reliable diagnosis
  • Immunocompromised (50%)
  • Bacteremia –> dissemination to brain (most common), soft tissue, retina

Imaging: Necrotizing cavitary pneumonia

  • Unilateral disease
  • Consolidation >> GGO:
    • lobar vs diffuse
    • Indistinct margins
  • Cavitations (40%)
  • Nodules (60%) or Masses (20%)
    • Solitary vs multiple
    • Well-defined, irregular borders
  • Pleural effusion +/- empyema
  • Lymphadneopathy
  • Bronchiectasis
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8
Q

Actinomycosis

A

Pathology:

  • Actinomyces: gram positive anaerobic saprophytic organism
  • Causes chronic granulomatous inflammation
  • Chronic clinical presentation
  • Malginancy needs to be excluded
  • Association: alcoholism, poor oral hygience, chronic conslidation

IMAGING:

  • Focal/pathcy consolidation + central low attenuation
    • Peripheral
    • Unilateral
    • Cavitations
  • Pleural effusion
  • Chest wall invovlement
  • Bronchiectatic form
  • Endobronchial actinomycosis –> bronchiolithiaisis/foreign body
  • Hilar/mediastinal lymphadenopathy

DDx:

  • Malignancy
  • Fungal infection
  • Other pneumonia
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9
Q

Tuberculosis

A

Pathology:

  • Mycobacterium tuberculosis:
    • highly aeorbic
    • Acid-fast/Ziehl-Neelson stain
  • Caseating granulomatous infection:
    • Central caseos necrosis
    • Surrounding macrophages, giant cells, lymphocytes
  • Ghon Focus: primary site of pulmonary TB causing caeseating granulomatous infection (Lung nodule)
  • Ghon complex: lung nodule + associated lymphadenopathy
    • TB drain freely or within phagocytes (with intra-cellular proliferation) from Ghon focus into regional lymph nodes –> ceseating granulomatous reaction in LN
    • TH1 Cell-mediated immunity controls infection (takes ~3weeks)
    • If heals –> fibrosis + calcification –> RANKE COMPLEX
  • Active vs latent: infective vs non-infective
  • TB infection:
    • Primary TB:
      • Initial infection of nonsensitized patients
      • Progressive primary TB in 5% - elderly/immunocompromised
    • Secondary TB (Post primary):
      • Reactivation TB due to impaired immunity
      • Exogenous re-infection
    • Miliary TB (primary/secondary may proceed to this)
      • ​Miliary pulmonary TB
        • Hematogenous spread: organism drains via lymphatics –> venous blood –> back to lungs
        • Often associated with immunosuppression
      • Miliary systemic TB: occurs when there is hematogenous spread via systemic arterial system (liver, bone, spleen, adrenals, meninges, kidneys, uterine tubes)

Epidemiology:

  • 1/3 of popoulation infected
  • Highest prevance: India, China, South Africa, Indonesia, Pakistan

Primary pattern:

  • Consolidation: segmental, lobar, multifocal
  • Atelectasis (children)
  • Lymphadneopathy: central, low attenuation with enhancing rim

Primary Progressive:

  • Consolidation +/- Cavitation
  • Acute bronchogenic dissemination/bronchiolitis:
    • Tree-in-bud
    • Centrilobular nodules
    • Lobular consolidation/GGO
  • Lymphadenopathy

Secondary/Post primary:

  • Upper lobe predominant: apical/posterior segments
  • Heterogenous consolidation: lobular/segmental/lobar, multifocal
  • Cavitation (45%): may erode into airways
  • Bronchiolitis:
    • Tree-in-bud
    • Centrilobular nodules
    • Lobular consolidations/GGO
  • Air-way invovlement:
    • Bronchial stenosis
    • Bronchial wall thickening
    • Volume loss/hyperinflation/postobstructive pneumonia
    • Tracheal/laryngeal invovlement (less common)
  • Nodules (tuberculomas):
    • Dominant lesion + satelite nodules
    • Calcifications
  • Pleural effusions
  • Lymphadenopathy (5%): pre-existince of hypersensitivity means that prompt and marked tissue response occurs that wall of foci of infeciton, prevents lymphatic spread

Complications:

  • Miliary TB: hematogenous spread –> random nodules
  • Tuberculous empyema
  • Mycetoma
  • Hemoptysis:
    • Rasmussen aneurysm (pulmonary artery pseudoaneurysm)
    • Hypertrophied bronchial arteries
  • ARDS
  • other:
    • ​Lung fibrosis
    • Nediastinal fibrosis
    • Endobronchial/endotracheal involvement: bronchostenosis, broncholithiasis
    • Malignancy
  • Hematogenous/lymphatic spread:
    • Organ invovlement:
      • Pott disease (discitis/osteomyelitis)
      • Meningitis
      • liver/spleen/adrenals/uterine tubes etc
    • Lymphadenities (scrofula)

Diagnosis: isolation and culture of MTB

Rx: isoniazid, rifampicin, streptomycin, ethambutol, pyrazinamide

DDx:

  • Sarcoid
  • Chronic fungal infection
  • Lung Ca
  • PMF
  • Ankylosing spondylitis
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10
Q

Nontubercululous Mycobacterial Infection

A

Pathology:

  • Mycobacterium Avium or Intracellulare complex (MAC)
    • Acid-fast bacilli within macrophages
    • May be disseminated throughout phagocyte sytem (LN, liver, spleen, localised to lungs)
    • Source: water
    • Cause granulomatous infection
  • Typically in T-cell immunodeficiency: disseminated infections
  • Atypically immunocompetent: tend to be isolated to lungs

Imaging:

  • General Features:
    • Slowly progressive bronchiectasis, nodules
    • Location: Middle lobe + lingular
  • Cavitary form (classic): INDISTINGUISHABLE FROM TB
    • Upper lobe predominance
    • Cavitation (thin-walled)
    • Pleural thickening
    • Consolidation/GGO/nodules/mass-like opacities
    • Bronchiolitis: centrilobular nodules, tree-in-bud
    • Lymphadenopathy
  • Bronchiectatic form (nonclassic)
    • Middle lobe/lingula bronchiectasis
    • Bilateral mutltifocal Bronchiolitis: tree-in-bud, centrilobular nodules, bronchial wall thickening, mucous plugging
    • Perbronchial nodules
    • Consolidation/GGO
    • Mosaic attenuation (small air-way disease)
    • Scarring, volume loss, archiectural distortion
  • Nodules
  • Immunocompromised:
    • hilar/mediastinal lymphadneopathy
    • Pleural effusions
  • Hypersensitivity pneumonia: airtrapping + centrilobular nodules

DDx:

  • TB
  • Other infection: cryptococcus, sporotrichosis, nocardiosis
  • Lung cancer
  • PMF
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11
Q

Mycoplasma Pneumoniae

A

Pathology:

  • Mycoplasma pneumoniae
  • Oedema/inflammatory cellular infiltrate in alveolar septa/peribronchovascular interstitium
  • Spread by respiratory droplets
  • Children + young adults (15-50% of pneumonias)

CT

  • Lower lobe predominance
  • Uni vs bilateral
  • Patchy consolidation
  • Bronchilolitis: centrilobular/peribronchovascular nodules/GGO, tree-in-bud, bronchial wall thickening
  • Lymphadenopathy
  • Small pleural effusions

Complications:

  • Pericarditis
  • Swyer-James-Mcleod syndrome
  • Bronchiectasis

Rx: macrolides/quinolones, supportive

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12
Q

Influenza Pneumonia

A

Influenza A/H1N1: lower respiratory tract viral infection

Radiograph:

  • Interstitial opacities
  • Nodular opacities
  • Extensive air-space disease
  • Progression to ARDS

CT:

  • Mosaic attenuation + air-trapping
  • GGO/Consolidation
  • Bronchiolitis: centrilobular nodules/GGO/consolidation, tree-in-bud
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13
Q

CMV pneumonia

A

Cytomegalovirus

Immunocompromised

General:

  • Diffuse or lower lung predominance

Radiograph:

  • Bilateral patchy or diffuse opacities
  • Small or large lung nodules
  • Consolidation: segmental/lobar
  • Plerual effusion

CT:

  • Consolidation: may be mass-like
  • Patchy or diffuse GGO
  • Nodules: random, bilateral
  • Bronchiolitis: tree-in-bud, bronchial wall thickening
  • Pleural effusions

DDx:

  • PCP
  • Viral pneumonia
  • Drug reaction
  • Lung transplant rejection
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14
Q

Histoplasmosis

A

Pathology:

  • Histoplasma capsulatum: fungus found in soil
  • Acquired by inhalation of dust particles from soil contaminated with bird/bad troppings containing spores
  • Found mainly in phagocytes and form a granulmoatous infection –> fibrose and calcify
  • Disease process is similar to TB:
    • Primary pulmonary invovlement that is often self limiting (produce coin lesions)
    • Chronic progressive secondary lung disease
    • Extrapulmonary spread
    • Diseeminated disease in immunocompromised

Rx:

  • Immunocompentent: resolves without treatment (99%)
  • Immunocompromised: antifungal

Imaging:

  • Acute histoplasmosis:
    • Airspace disease in any lobe/multifocal, lower lobe predominant
    • Ipsilateral hilar/mediastinal lymphadenopathy
    • Plerual/pericardia leffusion + caviatation
  • Chronic histoplasmosis:
    • Progressive upper lobe patchy opacities
    • volume loss
    • fibrosis/honeycombing
    • Emphysema/bullae
  • Disseminated disease: miliary nodules +/- cavitation
  • Histoplasmoma:
    • nodule +/- calcification (diffuse/central/laminated)
    • lung + mediastinum
  • Ipsilateral hilar/mediastinal lymphadenopathy + calcification (mimics ranke complex)
    • May be centrally necrotic
  • Fibrosing mediastinitis: soft tissue infiltration, causing narrowing of adjacent structures
  • Calcified hepatic/splenic granulomas
  • Broncholith
  • Middle lobe syndrome

Fluoroscopy: evaluate esophageal stenosis, fistula, diverticula

DDx:

  • TB (very similary)
  • Malignancy
  • Other fungal infection
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15
Q

Coccidioides Immitis

A

Pathology:

  • Inhalation of arthroconidia (type of spore) of Coccidioides immitis (fungus)
  • Delayed type hypersensitivity reaction –> granulomatous lesions (similar to histoplasma)
  • Incubation period 1-4 weeks
  • Asymptomatic (90%)
  • Symptomatic (10%) lung lesions/fevers/cough
  • Disseminated disease (<1%): immunosuppressed

Epi: endemic to arid regions of western hemisphere

Rx: amphotericin B if severe symptoms

Imaging:

  • Lobar consolidation/lung nodules (thick/thin grape skin walls) + cavitation
  • Hilar/mediastinal lymphadenopathy
  • Pleural effusion
  • immunocompromised

DDx:

  • Bacterial
  • Fungal
  • Mycobacterial
  • Cancer
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16
Q

Cryptococcus Neoformans

A

Pathology:

  • Cryptococcus neoformans (fungi)
  • Soil and bird shit (filthy pigeons) –> inhaled
  • Polysacchride Capsule: prevents phagocytosis, stains red with acid-shiff
  • Melanin production
  • Enzymes
  • Immuno compromised >> immunocompetent

Imaging:

  • Multiple pulmonary nodules +/- cavitation
  • Peripheral > central
  • Patchy airspace consolidation/GGO
  • CT halo
  • Mediastinal Lymphadenopathy
  • FDG avid (may mimic ca)

DDx:

  • SCC
  • Pulmonary mets
  • Septic emboli
  • Wegeners
17
Q

Aspergillosis

A

Pathology:

  • Aspergillus: inhaled as airborne conidia
  • Most infections caused by A.Fumigatus
  • Aspergiloma/mycetoma: colonisation of pulmonary cavities with minimal/no invasion of tissue
  • Invasive aspergillosis:
    • immunocompromised
    • Types:
      • Angioginvasive: invade vessels, cause necrosis + hemorrhage and disseminate hematogenously
      • Airway invasive: predominantly effect air awys
      • Subacute
  • Form fruiting bodies, septate filaments with acute angle hypae (45degree)
  • can cause allergic reactions (ABPA) especially in asthmatics

Aspergilloma:

  • Dependent, spehrical/ovoid nodule in preexsiting cavity
  • Surrounding gas (Monad sign) - implies mobile mass

Invasive asperigilloma:

  • Solitary/multifocal consolidation, mass or centrilobular nodules/GGO
  • CT Halo sign (early): central nodule/consolidation with surrounding GGO (hemorrhage)
  • Air-Cresent Sign (late):
    • Cresenteric shaped gas collection WITHIN nodule/mass/consolidation
    • Indicates recovery/healing
    • Consistent with invasive aspergiolosis in immunocompromised patient
  • Occluded vessel sign: peripheral segmental PA at lesion edge
  • Hypodense (early): central hypodensity in nodule/mass/consolidation due to infarction
  • Peripheral wedge shape consolidation: pulmonary infarct
  • Airway invasion:
    • Tracheal/bronchial ulcerations
    • Bronchiolitis
    • Bronchopneumonia
  • May cavitate (semi-invasive)
  • No lymphadenopathy/plerual effusion

DDx:

  • Infection: fungal, mycobacterial, bacterial, septic emboli
  • Non-small cell lung cancer
  • Pulmonary infarct
  • Inflammattory: wegeners
18
Q

Pneumocystis Jirovici

A

Pathology:

  • Fungus: Pnumocystis Jiroveci
  • Opportunistic fungal infectious agent as usually of low virulence.
  • Immunocompromised: CD4 <200, long term steroids, organ transplant, chemo
  • Intra-alvoelar foamy exudate with fungus in tinty bubble-like areas:
    • Gomori methanamine silver/calcufluor white stain
  • Rare as most receive prophylaxis (co-trimoxazole)

Imaging:

  • Location: diffuse perihilar + subpleural/peripheral sparing (often spares 1 lung zone)
  • GGO (92%)
    • +/- intralobular lines
    • +/- interlobular septal thicekning (crazy paving)
  • Cysts (30%): thin walled + GGO, typically upper lobe. Resolves with Rx. Associated with pneumothorax.
  • ARDS: consolidation
  • Atypical:
    • mutliple small nodules +/- cavitation
    • lobar consolidation
    • mass
    • lymphadenopathy
    • pleural effusion
    • Mosaic attenuation
  • chronic PCP:
    • ​Irregular linear opacities
    • Fibrosis: archiectural distortion, traction bronchiectasis
    • Large nodules

DDx:

  • Hypersensitivity pneumonitis
  • Lymphocytic intersitial pneumonia
  • Diffuse alveoalr hemorrhage
  • Infection: CMV
  • Non-cardiogenic oedema
  • Pulmonary alveolar proteinosis