000 Solitary Pulmonary Nodule (SPN)

    • Etymology Derived from the Latin “nodulus,” meaning small knot or lump.
    • AKA and abbreviation SPN (Single Pulmonary Nodule).
    • What is it? A single, discrete, round or oval lesion within the lung parenchyma, measuring between 3 mm and 30 mm in diameter, surrounded by normal lung tissue and not associated with lymphadenopathy, atelectasis, or pleural effusion. Lesions smaller than 3 mm are classified as micronodules and are not included in the SPN category.
      • Ground-glass nodules (GGNs) greater than 3 mm are considered SPNs if solitary and not associated with additional abnormalities.
    • Characterized by Characterized by:
      • Discrete round or oval opacity surrounded by normal lung parenchyma.
      • Lesion size between 3 mm and 30 mm; anything larger is categorized as a mass, while anything smaller is classified as a micronodule.
      • Can be solid, partially solid (subsolid), or ground-glass in density.
      • Sharp or poorly defined margins.

      Characteristics:

      • Smooth: Often benign (e.g., granuloma).
      • Lobulated: Suggests malignancy due to differential growth rates.
      • Spiculated: Highly suspicious for malignancy.
      • Calcifications:
        • Central/popcorn: Suggest benignity (e.g., granuloma and less common hamartoma).
        • Eccentric/stippled: Suspicious for malignancy.
        • Lobular: May be associated with specific conditions such as amyloid deposits or Castleman’s disease.
      • Cavitating: May indicate necrosis within a lesion; implications include possible malignancy, infections (e.g., tuberculosis), or vascular abnormalities.
      • Fat-containing: Typically benign and associated with hamartomas; may also indicate lipomatous components or teratomas.
    • Caused by
      • Most Common Cause(s):
        • Granulomas (e.g., tuberculosis, histoplasmosis).
        • Malignancies (e.g., primary lung cancer or metastasis).
        • Benign neoplasms (e.g., hamartomas).
      • Other Causes Include:
        • Inflammatory conditions:
          • Granuloma.
          • Lung abscess.
          • Rheumatoid nodule.
          • Pulmonary inflammatory pseudotumor: plasma cell granuloma.
          • Small focus of pneumonia: round pneumonia.
        • Infections: Fungal or bacterial infections.
        • Circulatory abnormalities:
          • Arteriovenous malformations.
          • Pulmonary artery aneurysm.
          • Pseudoaneurysm.
          • Pulmonary infarct.
          • Pulmonary hematoma.
        • Congenital lesions:
          • Arteriovenous malformation.
          • Lung cyst.
          • Bronchial atresia with mucoid impaction.
        • Infiltrative conditions:
          • Amyloid deposits.
          • Castleman’s disease.
        • Miscellaneous causes:
          • Intrapulmonary lymph node.
          • Mucoid impaction.
          • Normal confluence of pulmonary veins.
    • Resulting in: Variable clinical symptoms, ranging from asymptomatic findings on imaging to cough, hemoptysis, or systemic symptoms if malignant.
    • Structural changes: Disruption of normal lung architecture with possible central necrosis, cavitation, or fibrosis.
    • Pathophysiology: The pathogenesis varies depending on the underlying cause. Malignant nodules arise from uncontrolled cellular proliferation, while benign nodules may result from inflammation, infection, or developmental anomalies.
    • Pathology:
      • Benign: Organized inflammation, fibrous tissue, or congenital defects.
      • Malignant: Dysplastic cells with abnormal architecture, nuclear pleomorphism, and necrosis.
    • Diagnosis:
      • Clinical history and risk factors (e.g., smoking, exposure to carcinogens).
      • Imaging evaluation (e.g., size, shape, margins, and density on CT).
      • Tissue sampling (e.g., biopsy or resection) if imaging is inconclusive.
    • Clinical: Typically asymptomatic; symptoms are more common in malignancies or infections.
    • Radiology Detail:
      • CXR:
        • Findings: Single, well-circumscribed round opacity.
        • Associated Findings: Absence of lymphadenopathy, pleural effusion, or atelectasis.
      • CT:
        • Parts: Matrix and border.
        • Size: 3 mm to 30 mm.
        • Shape: Round, oval, irregular, spiculated, or lobulated.
        • Position: Variable, depending on underlying etiology.
        • Character:
          • Solid, ground-glass (GGN), or part-solid.
          • Calcifications:
            • Central, eccentric, irregular, psammomatous.
          • Fat.
          • Cavitation.
        • Time:
          • Stability over 2 years suggests benignity.
          • Malignant nodules typically double in size within 20-400 days.
            • For example:
              • A 3 mm malignant nodule may grow to approximately 4 mm to 5 mm within 60-90 days.
              • A 5 mm malignant nodule may grow to approximately 6-7 mm within 60-90 days.
              • A 7 mm malignant nodule may grow to approximately 9-10 mm within 60-90 days.
              • A 10 mm malignant nodule may grow to approximately 12-14 mm within 60-90 days.
          • GGNs grow more slowly than solid nodules, often necessitating prolonged follow-up to detect late malignant transformation.
        • Associated Findings: Calcification patterns, spiculation, or cavitation.
      • Other relevant Imaging Modalities:
        • PET CT/NM/Useful for metabolic activity assessment (e.g., PET) or better tissue characterization (e.g., MRI).
    • Pulmonary function tests (PFTs): Rarely required unless nodule-associated respiratory compromise is suspected.
    • Recommendations: Follow Fleischner Society Guidelines for nodule management based on size, appearance, and patient risk factors:
      • For solid nodules:
        • <6 mm: No routine follow-up required for low-risk individuals; optional follow-up for high-risk patients.
        • 6-8 mm: Follow-up CT at 6-12 months, then consider additional CT at 18-24 months if no growth.
        • >8 mm: Follow-up CT at 3 months, PET/CT, or tissue sampling based on patient risk factors and clinical context.
      • For subsolid nodules (GGNs):
        • <6 mm: No routine follow-up required.
        • >6 mm: Initial follow-up CT at 6-12 months, then annual surveillance for 5 years.
        • Part-solid nodules >6 mm: Special attention is warranted to the solid component. Follow up with CT in 3-6 months; further management depends on stability or growth.
    • Key Points and Pearls:
      • Small, smooth, calcified nodules are likely benign.
      • Nodules with spiculation or eccentric calcifications warrant further evaluation.
      • Follow-up CT at appropriate intervals is crucial for risk stratification.
      • Ground-glass nodules (GGNs) larger than 3 mm may represent SPNs and require long-term monitoring due to their potential for slow malignant transformation.  GGNs generally grow more slowly than solid nodules, necessitating prolonged observation.