000 Pneumonia

  • What is it:
    • Pneumonia
      • typically associated with infection
      •  BUT
      • is a relatively non-specific term,
      • refers to:
        • A radiological finding characterized by
          • lung parenchymal opacities,
      • The term “pneumonia” historically referred to
        • any lung inflammation before the infectious etiology was established.
        • many ILDs for example are considered “pneumonias” and share overlapping imaging features
          • e.g.,
          • consolidation
          • ground-glass opacities,
          • fluid accumulation
          • interstitial process
          • fibrosis
        • contributing to diagnostic confusion.
    • typically associated with
            • infection (e.g., bacteria, viruses, fungi),
          • but other pneumonias include
            • non-infectious inflammatory processes.:
              • e.g.,
              • aspiration, or
              • radiation injury).
            • also used to label interstitial lung disease (ILD) patterns, including:
              • Non-Specific Interstitial Pneumonia (NSIP),
              • Usual Interstitial Pneumonia (UIP).
              • Lymphocytic Interstitial Pneumonia (LIP),
              • Cryptogenic Organizing Pneumonia (COP)
              • Acute Interstitial Pneumonia (AIP)
              • Desquamative Interstitial Pneumonia (DIP)
              • Eosinophilic Pneumonia (EP)
    • Clinical, laboratory, and microbiological correlation is essential to establish the underlying etiology.
  • Etymology:
    • Derived from the Greek word pneumon (lung) and the suffix -ia (condition), meaning “condition of the lung.”
  • AKA:
    • Pulmonary infection, Lung inflammation (when non-infectious).
  • How does it appear on each relevant imaging modality:
    • Chest X-ray:
      • Lobar pneumonia:
        • Homogeneous opacity confined to one lobe or segment.
        • May show the air bronchogram sign (air-filled bronchi within consolidated lung).
      • Bronchopneumonia:
        • Patchy, peribronchial opacities scattered throughout both lungs.
      • Interstitial pneumonia:
        • Reticular or ground-glass opacities, often bilateral and diffuse.
      • Associated findings:
        • Pleural effusion, cavitation, or lymphadenopathy in complicated cases.
    • Chest CT:
      • Parts:
        • Involves alveoli, interstitium, or both.
      • Size:
        • Localized (lobar or segmental) or diffuse (multifocal or bilateral).
      • Shape:
        • Confluent, patchy, or reticular depending on the type.
      • Position:
        • Lobar: Often unilateral and segmental.
        • Bronchopneumonia: Diffuse, peribronchial distribution.
        • Interstitial: Diffuse, peripheral, or lower lobe predominant.
      • Character:
        • Consolidation (dense opacity with air bronchograms).
        • Ground-glass opacities (less dense, representing alveolar/interstitial filling).
      • Time:
        • Resolves with treatment but may evolve into complications (e.g., abscess, fibrosis).
    • Ultrasound:
      • Useful for detecting:
        • Subpleural consolidations.
        • Associated pleural effusions.
    • MRI:
      • Rarely used but may highlight soft-tissue involvement in cases of necrotizing pneumonia or empyema.
  • These findings reflect:
    • Infectious pneumonia:
      • Bacterial:
        • Streptococcus pneumoniae (lobar pneumonia).
        • Staphylococcus aureus (abscess, pneumatoceles).
      • Viral:
        • Influenza, RSV, or COVID-19 (diffuse, interstitial opacities).
      • Fungal:
        • Aspergillus or Histoplasma (nodular or cavitary lesions).
    • Non-infectious inflammatory pneumonia:
      • Organizing pneumonia (e.g., cryptogenic or secondary to autoimmune disease).
      • Aspiration pneumonia (dependent lobe involvement).
  • Differential diagnosis:
    • Non-infectious lung disease:
      • Pulmonary edema (cardiogenic or non-cardiogenic).
      • Atelectasis (volume loss with shift of structures).
      • ARDS (acute respiratory distress syndrome).
    • Infectious mimics:
      • Tuberculosis.
      • Fungal infections (e.g., histoplasmosis, coccidioidomycosis).
    • Malignant mimics:
      • Bronchoalveolar carcinoma.
      • Lymphoma with pulmonary involvement.
  • Recommendations:
    • Correlate imaging findings with clinical symptoms (e.g., fever, cough, dyspnea) and laboratory markers (e.g., elevated WBC count, positive cultures).
    • Perform Chest CT if:
      • Findings are atypical or diagnostic uncertainty persists.
    • Consider bronchoscopy or lung biopsy in cases of non-resolving pneumonia to exclude malignancy or non-infectious etiologies.
    • Use follow-up imaging to confirm resolution, particularly in high-risk patients.
  • Key points and pearls:
    • Pneumonia findings on imaging are non-specific and require clinical correlation to establish the etiology since it spans a broad group of findings that include
      • consolidation
      • ground-glass opacities,
      • fluid accumulation
      • interstitial process
      • fibrosis
    • Air bronchograms are a hallmark of consolidation and strongly suggest alveolar filling.
    • Lobar pneumonia is often bacterial, while interstitial patterns suggest viral or atypical organisms.
    • Pneumonia may mimic or co-exist with malignancies or chronic lung diseases; persistent findings warrant further evaluation.
    • Ultrasound is particularly valuable for bedside assessment in critically ill patients.

 

 

Pneumonia Etmology

  • The word “pneumonia”
    •  from the Greek word
      • “pneumon,” which means “lung.” and
      • “-ia,” which is a suffix used to indicate a condition or state.
  • Therefore, “pneumonia” translates to
    • “lung condition” or
    • “lung disease” in Greek. This is fitting given that pneumonia is a respiratory condition characterized by inflammation of the lungs, often caused by infection.

Infection

  • Pneumonia
    • general term
      • filling the alveoli.
      • usually purulent, (ie infection)
    • generally caused by infecction but entities such as DIP (Desquamative Interstitial Pneumonia), LIP (Lymphocytic Interstitial Pneumonia), NSIP (Nonspecific Interstitial Pneumonia), UIP (Usual Interstitial Pneumonia), COP (Cryptogenic Organizing Pneumonia), and OP (Organizing Pneumonia)—refer to specific patterns of interstitial lung diseases and are called  pneumonia but they  fall under the broader category of pneumonitis, or inflammation of the lung tissue.

Pneumonias can be classified by:

  • etiology
    • infective agent
      • bacterial (pyogenic) pneumonia
        • cavitating bacterial pneumonia
      • fungal pneumonia
        pneumocystis pneumonia (PCP)
        mycobacterial pneumonia
        viral pneumonia
        coronavirus
        COVID-19
        Middle East respiratory syndrome (MERS) infection
        severe acute respiratory syndrome (SARS)
        varicella pneumonia
        setting of infection
        community-acquired pneumonia
        hospital-acquired pneumonia (HAP)
        ventilator-associated pneumonia (VAP)
        healthcare-acquired pneumonia (HCAP)
        aspiration pneumonia
        lipid: lipoid pneumonia
        method of spread (a pathological description)
        bronchopneumonia
        lobar pneumonia
        multilobar pneumonia
        radiographic appearance
        atypical pneumonia
        round pneumonia
        cavitating pneumonia
        hemorrhagic pneumonia

 

TB
Reactivation TB
CXR reveals a dense consolidation in the right upper lobe (red arrow) with questionable air-fluid level. No pneumothorax. No pleural effusions. Differential includes right upper lobe pneumonia or tuberculosis. CT is recommended for further evaluation if there is concern for a cavity.
Courtesy Joseph Cannella,
Dr. Christina LeBedis, MD, MS
CTPA reveals a large consolidation in the right upper lobe and superior segment of the right lower lobe spans approximately 8.8 x 5.6 x 9.4 cm and extends to the pleura. There are multiple internal cavitations (red arrows) with air-fluid levels. These large predominately right upper lobe cavitary lesions are consistent with clinical concern for tuberculosis pneumonia, however follow-up with chest CT in 3 months post-treatment is recommended to exclude other less likely causes of cavitary lesions, such as malignancy.
Courtesy Joseph Cannella,
Dr. Christina LeBedis, MD, MS

Bronchopneumonia- Centrilobular

lung axial interstitium bronchioles connective tissue fx bronchial plugging peribronchial halo peribronchial thickening dx bronchopneumonia CTscan Davidoff MD 47614c01

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