Eosinophilic pneumonia differential diagnosis: Difference between revisions
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|Eosinophilic granulomatosis with polyangitis | |Eosinophilic granulomatosis with polyangitis | ||
| | |3 phases: | ||
* rhinosinusitis and asthma | |||
* blood and tissue eosinophilia, | |||
* systemic vasculitis | |||
* Asthma is always present in EGPA, | |||
* Chronic rhinitis in 75% of cases | |||
* chronic paraseptal sinusitis and nasal polyposis | |||
* asthenia, weight loss, fever, arthralgias, | |||
* Glomerulonephritis | |||
* Eosinophilic myocarditis and coronary arteritis may cause heart failure | |||
| | | | ||
* Peripheral blood eosinophilia: Between 5 and | * Peripheral blood eosinophilia: Between 5 and | ||
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* ANCAs are found in only 40% of patients | * ANCAs are found in only 40% of patients | ||
| | | | ||
* Pulmonary infiltrates: ill-defined opacities with peripheral predominance | |||
* ground-glass opacities | |||
* airspace consolidation. | |||
* centrilobular nodules | |||
* bronchial wall thickening | |||
* Interlobular septal thickening | |||
* hilar or mediastinal lymphadenopathy | |||
* pleural effusion | |||
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Revision as of 02:35, 12 February 2018
Eosinophilic pneumonia Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Acute eosinophilic pneumonia may be differentiated from other causes of pulmonary eosinophilia
Acute eosinophilic pneumonia (AEP)
- The cause of acute eosinophilic pneumonia is unknown.
- Some investigators have suggested that AEP is an acute hypersensitivity reaction to an unidentified inhaled antigen in an otherwise healthy individual [1].
Transpulmonary passage of helminth larvae (Löffler syndrome)
- Three types of helminths, Ascaris (A. lumbricoides, A. suum), hookworms (Ancylostoma duodenale, Necator americanus), and Strongyloides stercoralis, have larvae that reach the lungs, penetrate into alveoli, and ascend the airways then reach the gastrointestinal tract. [10]
- Ascaris is the most common cause of Löffler syndrome worldwide. [11]
Tropical pulmonary eosinophilia
- Tropical pulmonary eosinophilia is immune response to the bloodborne microfilarial stages of the lymphatic filariae and Wuchereria bancrofti. [16-18].
- The typical symptoms are cough, breathlessness, wheezing, fatigue, and fever. Pulmonary function tests may show a mixed restrictive and obstructive abnormality with a reduction in diffusion capacity. [18]
Eosinophilic granulomatosis with polyangitis
- Eosinophilic granulomatosis with polyangiitis (Churg-Strauss) is a vasculitic disorder often characterized by sinusitis, asthma, and prominent peripheral blood eosinophilia. [49]
- It is the sole form of vasculitis that is associated with both eosinophilia and frequent lung involvement. In addition to the lungs, the skin and the cardiovascular, gastrointestinal, renal, and neurologic systems may also be involved.
Allergic bronchopulmonary aspergillosis
- Allergic bronchopulmonary aspergillosis (ABPA) is a complex hypersensitivity reaction that occurs when airways become colonized by Aspergillus. [51]
- Repeated episodes of bronchial obstruction, inflammation, and mucoid impaction can lead to bronchiectasis, fibrosis, and respiratory compromise.
- Immunologic responses elicited by Aspergillus fumigatus are responsible for this syndrome.
Drugs and toxins
Drug reaction with eosinophilia and systemic symptoms (DRESS) is a drug-induced hypersensitivity reaction that includes skin eruption, eosinophilia, atypical lymphocytosis, lymphadenopathy, and kidney involvement. Drugs causing DRESS are:
- Nonsteroidal anti-inflammatory drugs (NSAIDs) [26]
- anticonvulsants
- antidepressants
- angiotensin converting enzyme inhibitors
- beta blockers
- hydrochlorothiazide
- sulfa-containing compounds [27]
Differential Diagnosis
Clinical Picture | Laboratory diagnosis | Imaging | Treatment | |
---|---|---|---|---|
Acute eosinophilic pneumonia | Onset <1 month | |||
Chronic eosinophilic pneumonia | Onset >2–4 week | |||
Transpulmonary passage of helminth larvae | ||||
Allergic bronchopulmonary aspergillosis | ||||
Eosinophilic granulomatosis with polyangitis | 3 phases:
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20,000/mm
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