The Other P.I.E.
Pulmonary Infiltrates With
Eosinophilia
Eosinophilic Lung Disease
The Other P.I.E.
Pulmonary Infiltrates With
Eosinophilia
Eosinophilic Lung Disease
© William Herring, MD, FACR
Pulmonary Infiltrates with
Eosinophilia
Pulmonary disease affecting major
airways and/or lung parenchyma
associated with blood and/or tissue
eosinophilia
Eosinophilic Lung Disease
Classification by Clinical Severity
Benign
Loeffler’s syndrome
Intermediate
Eosinophilic pneumonia
Severe
Hypersensitivity Angiitis
Polyarteritis nodosa
Idiopathic
Associated With Specific Etiology
Associated with Connective Tissue
Disease or Vasculitis
Eosinophilic Lung Disease
Classification by Etiology
Loeffler’s syndrome
Acute Eosinophilic Pneumonia
Chronic Eosinophilic Pneumonia
Hypereosinophilic syndrome
Eosinophilic Lung Disease
Idiopathic
Atopic history common
May be asymptomatic or very symptomatic
High fever and dyspnea
Associated with blood eosinophilia
Biopsies also show eosinophils in infiltrate
Loeffler’s Syndrome
General Considerations
May present as
reverse pulmonary edema
Infiltrates may be single or multiple
Usually transitory airspace opacities
Reduction in size of one infiltrate in 24
hrs with appearance of a 2nd is
suggestive
Infiltrates are usually peripheral
Loeffler’s Syndrome
Imaging Findings
Loeffler’s syndrome
Chronic Eosinophilic Pneumonia
General
Very rare disease (188 cases)
More protracted course than Loeffler’s
Atopic history
Female:male 2:1
Chronic Eosinophilic Pneumonia
Pathology
High levels of circulating IgE
Eosinophilic abscesses in lung
Blood eosinophilia
Pathologically identical to Loeffler’s
Chronic Eosinophilic Pneumonia
X-ray
Similar to Loeffler’s except infiltrates
last for many days or week without
steroids
Chronic Eosinophilic Pneumonia
Clinical
Most are asymptomatic or mild symptoms
Some have
High fever
Malaise
Weight loss
Respond within days to steroid therapy
Idiopathic
Associated With Specific Etiology
Associated with Connective Tissue
Disease or Vasculitis
Eosinophilic Lung Disease
Classification of PIE by Etiology
Eosinophilic Lung Disease
Specific Etiology
Drug-induced
Nitrofurantoin
Penicillin
Sulfonamides
Parasite-induced
Ascariasis
Paragonomiasis
Parasite-induced
Strongyloidiasis
Tropical
Eosinophilia
Fungus-induced
ABPA
Eosinophilic Lung Disease
Drug-induced
Interstitial edema
Most commonly nitrofurantin
Patchy, fleeting air space disease
Amiodarone
Penicillin
Sulfonamides
Hydrochlorthiazide
Nitrofurantoin (Furadantin)
Disease
disappears
shortly after
removal of
antibiotic
Amiodarone
Eosinophilic Lung Disease
Parasite-induced
Most often from Ascaris lumbricoides
Caused by the larva as they pass
through lungs
Allergic response of patchy, fleeting
infiltrates
Blood eosinophilia
Idiopathic
Associated With Specific Etiology
Associated with Connective Tissue
Disease or Vasculitis
Eosinophilic Lung Disease
Classification of PIE by Etiology
Rheumatoid Disease
Granulomatosis with Polyangiitis
(Wegener’s Granulomatosis)
Allergic Granulomatosis
Polyarteritis Nodosa
Eosinophilic Lung Disease
Connective Disease or Vasculitis
Multiple nodules of
varying sizes with
frequent cavitation
Granulomatosis with Polyangiitis
The End