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Infections

Infections . Pneumonia. 6 th leading cause of death in the US 1st leading cause of death by infection Early diagnosis by the clinician is key to decreasing morbidity and mortality and expenses for treating pneumonia. Role of Imaging in Pneumonia. Diagnosis of infection

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Infections

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  1. Infections

  2. Pneumonia • 6th leading cause of death in the US • 1st leading cause of death by infection • Early diagnosis by the clinician is key to decreasing morbidity and mortality and expenses for treating pneumonia

  3. Role of Imaging in Pneumonia • Diagnosis of infection • Recognition of complications • Not necessarily pathogen diagnosis • Organisms may cause more than one radiographic pattern • Most useful when read in setting of clinical diagnosis.

  4. Radiographic patterns • Lobar- Most common associations S. pneumo and K. Pneumo • Lobular (broncho pneumonia)-Mycoplasma most commonly associated • Interstitial-viruses • Lobar and bronchopneumonia are alveolar filling pneumonias- consolidation • Interstitial pneumonia will look like too many lines

  5. Associated findings • air bronchograms • the silhouette sign • parapneumonic effusions

  6. Lobar pneumonia S. pneumoinae K. pneumoniae Also seen with Legionella, Mycoplasma, H. Influenza Bronchopneumonia Gram-’s, anaerobes Legionella Actinomycosis Nocardia Mycoplasma Typical, atypical Tb Parasites Etiologic agents

  7. Radiographic patterns • Lobar pna tends to be homogeneous • Prominent air bronchograms • Preserved volume- vs atelectasis

  8. Bronchopneumonia Tends to be heterogeneous, patchy, coarse and irregular Can be difficult to differentiate from interstitial pna Radiographic patterns

  9. Radiographic patterns • Interstitial pna • Usually viral pnas • Influenza A,B,C • Parainfluenza • RSV • Adneoviruses • Herpes viruses • SARS • “Too many lines”

  10. Complications of Pneumonias • Pleural infection- • Empyema- purulent exudate,WBC > 25,000 and positive organisms

  11. Complications of Pneumonias • Cavitation • Cavitary pneumoina • Lung abscess • Pneumatocele • Gangrene

  12. Complications of Pneumonias • Pneumatocele- Ball-valve mechanism • Most common with S. aureus

  13. Complications of Pneumonias • Bronchiectasis-dilatation of bronchi usually due to chronically impacted bronchi with mucus increasing pressure • Common with atypical Tb and aspergillus

  14. Caution! • Beware of nonresolving consolidation • There are noninfectious causes of chronic consolidation- especially in elderly people • Ex include • Bronchoalveolar Carcinoma • Eosinophilic pna • Cryptogenic organizing pna • Consider consult or biopsy!

  15. Tuberculosis • Primary tuberculosis- can present without sx and normal chest x-ray, • Can appear with lobar consolidation in any lobe with preference for upper lobes, adenopathy, atelectasis and pleural effusion • Adenopathy is usually unilateral, usually on the right or paratracheal- more common in children • Pleural effusion more common in adults • Cavitation is RARE! • Usually heals with calcification-granulomas and calcified Lymph nodes

  16. Primary Tb

  17. Tuberculosis • Post primary Tb • Reactivation Tb-Usually in adults is a reactivation of a focus acquired in childhood • Limited to apical and posterior segments of upper lobes and superior segments of lower lobes • Healing occurs with contraction and fibrosis • Patterns- • Cavitation is common with thin walled cavity • Transbronchial spread – ex from one upper lobe to contralateral lower lobe • Bronchostenosis-narrowed airways • Pleural effusion- direct extension to pleural cavity • Direct extension to ribs

  18. Reactivation Tb

  19. Miliary Tb • Hematogenous spread of bacilli during primary Tb infection • Fever, chills, night sweats • 1mm nodules initially

  20. Aspergillus • Ubiquitous fungus • May result in disease when inhaled in susceptible hosts • Infection usually occurs in immunocompromised hosts • Degree of immunocompromise determines pattern of infection

  21. Aspergillus • Main patterns of infection • Decreased immunity • Invasive aspergillosis – angioinvasive, airway invasive • Chronic necrotizing • Normal Immunity • Aspergilloma • Hyperimmunity • Allergic bronchopulmonary aspergillosis (ABPA) • Hypersensitivity pneumonitis

  22. Angioinvasive • Severe immunocompromise- BMT, AIDS, high dose steroids, hematogenous malignancy • Maximal Risk: WBC < 500 cells/mm3 • Patchy consolidation and nodules that have ground glass halo, which then cavitate when neutropenia improves ( “ air cresecent sign”

  23. Angioinvasive

  24. Aspergilloma • Occur in pre-existing cavity in upper lobes- COPD, Bronchiectasis, Sarcoid • Cavity with internal opacity- opacity is mobile and demonstrates air crescent sign

  25. ABPA • Occurs with systemic hypersensitivity • Occurs usually in asthmatics • Eosinophilia documented • Components • Bronchiectasis- mid and upper lungs, centrally • Mucoid impaction- transient and recurrent- “gloved finger”

  26. ABPA

  27. Mediastinum • The key to the mediastinum is knowing the anatomy and what resides in each compartment • Pathology includes a range of tumors as well as infections, congenital abnormalities, vascular malformations, cardiac pathology and esophageal pathology

  28. Mediastinal Compartments • Anteriorsuperior (retrosternal space)- includes the thymus, the extrapericardial aorta and its branches, the great veins, and lymphatic tissue • Middle-includes the heart, intrapericardial great vessels, pericardium, and trachea • Posterior- includes the esophagus, vagus nerves, thoracic duct, sympathetic chain, and azygous venous system,and extends to the posterior aspect of the vertebral bodies and posterior ribs.

  29. Mediastinum

  30. Anterior mediastinum • Masses- differential diagnosis • The 4 “T”’s- not all inclusive- but includes majority • Thymus tumors- Thymoma, thymolipoma • Teratoma- and other Germ Cell tumors (e.g. seminoma) • Thyroid goiter • Terrible Lymphoma

  31. Anterior mediastinum • Radiology: • Terrible Lymphoma: big bulky LAD, absence of calcification is a discriminating feature • Thymomas- Age over 40, 20-25% contain calcium, solid and well defined, unilateral, can be cystic . Associated with Myasthenia Gravis • Teratomas (Germ Cell tumors)predominately cystic, age < 40.  Often calcification or fat  • Thyroid goiter/CA is continuous with thyroid in neck, high attenuation (iodine) – usually superior mediastinum

  32. Where is the mass?

  33. Anterior mediastinal mass • Anterior- crosses midline- germ cell tumor or lymphoma

  34. Substernal Goiter

  35. Thymoma- > age 40, typically solid, can have peripheral thin calcifications, can be cystic, usually to one side of midline

  36. Morgagni Hernia

  37. Middle medisatinum • Tumors of the middle mediastinum include pericardial cysts, bronchogenic cysts and lymphomas. A middle mediastinal mass may also represent lymphadenopathy as a result of infectious, malignant (metastatic), and idiopathic (eg sarcoidosis) etiologies. • Mediastinitis from prior granulomatous disease

  38. Middle mediastinal masses • Pericardial cyst Bronchogenic cyst

  39. Fibrosing mediastinitis • Notice soft tissue thickening surrounding trachea and narrowing it after histoplasmosis infection. Esophagus may be obliterated.

  40. Posterior mediastinal mass

  41. Posterior Mediastinum • Neurogenic tumor:  Schwannoma, neurofibroma, ganglioneuroma, neuroblastoma • Enteric/neurenteric cyst • Lateral thoracic meningocele • Osteocartilaginous tumor • Pulmonary mass or consolidation abutting mediastinum • Extramedullary hematopoesis • Paraspinal abscess, hematoma

  42. Posterior mediastinal mass • Paraspinal ganglioneuroma- notice intimacy with spinal canal and mass effect on trachea

  43. Aortic Aneurysm • Anuerysm can occur in any part of the mediastinum depending on where the aneurysm occurs, so consider it in all your differentials

  44. Nodules and Masses

  45. Definitions • Nodule: any pulmonary lesion represented in a radiograph by a sharply defined, discrete, nearly circular opacity ranging from 2-30 mm • Mass= nodule > 3 cm • Not all masses or nodules are malignant, but frequency of malignancy is higher in masses

  46. Solitary Pulmonary Nodule • What should you do next?

  47. Diagnostic Dilemma • Solitary Pulmonary Nodule- What do you do with it? • Options- compare with old films, get follow up films, CT scan, PET scan, biopsy or lung resection • Multiple guidelines have been issued and are confusing • Clinicians must consider age of the patient and risk factors such as smoking for possibility of cancer • Certain radiologic characteristics can help suggest that a nodule or mass is benign or malignant • Calcification pattern- central, popcorn or lamellated are benign • Fat within lesion- suggests hamartoma, benign • Spiculated margins and distortion of vessels suggests malignancy • Cavitation can occur in either- but malignant tumors have thicker walled cavities • Stability in size for 2 years • Double in volume equals increase in diameter by 25%- suggests malignant

  48. Diagnostic Considerations • Neoplasm - Primary malignancy- Small Cell, Squamous Large Cell, Adenocarcinoma - Metastasis - Benign – hamartoma Infection: fungus, prasites, abscess Congenital: sequestration, CCAM Non- infectious inflammatory- Wegener’s Granulomatosis Non- parenchymal lesions

  49. Solitary Pulmonary Nodule • Nodule has central fat suggesting hamartoma. • No more work up necessary. • Also can see popcorn calcifications which is also characteristic

  50. Malignant Primary neoplasms of lungs • Adenocarcinoma- (50%) most common, usually peripheral, low association with smoking, slow growth and early metastasis • Large Cell- (5%)Peripheral mass, nonspecific appearance, least • Squamous Cell (25%)–Central, endobronchial, Pancoast Tumor, most likely to cavitate, high association with smoking • Small Cell (20%)- Central, perihilar, SVC syndrome, Paraneoplastic sydromes, Fast growing and early mets

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