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Author Spotlight: Investigating the Pathophysiology of Eosinophilic Esophagitis
Published on: May 10, 2024
Reconsideration of discrepancies between clinical and histopathological features in acute eosinophilic pneumonia
H Mochimaru1, Y Fukuda, A Azuma
1. mochi123@dj8.so-net.ne.jp.
Background And Objectives:
Acute eosinophilic pneumonia (AEP) is a very rare condition, with only one paper published so far discussing histopathological findings at surgical biopsy. In that paper, AEP is considered to be an acute and proliferative stage of DAD accompanied by eosinophilia. However, acute respiratory distress syndrome, acute interstitial pneumonia, and acute exacerbation of idiopathic pulmonary fibrosis, which, unlike AEP are mostly life-threatening diseases, also exhibit DAD. AEP also presents with severe hypoxia but rapidly improves on treatment with corticosteroids alone, without subsequent fibrosis. In contrast, the other above-mentioned diseases with the same histopathology show greatly different clinical courses. The reasons for these differences remain unclear.
Methods:
Here we investigated the histopathology of AEP in 2 surgical lung biopsy and 14 transbronchial lung biopsy cases. Additionally, we determined the presence or absence of different phases of DAD by histopathology in these AEP cases.
Results And Conclusion:
Characteristic histopathological findings of AEP consist of alveolar edema with infiltration of eosinophils and lymphocytes and edema of perivascular area and interlobular septa. The alveolar spaces showed fibrinous exudates. There were no hyaline membranes or massive intraluminal fibrosis. These histopathological findings of interstitial edema and fluid exudates are consistent with radiological findings of lung edema and can explain the rapid and complete improvement.Because AEP does not exhibit lung fibrosis histopathologically, it should not to be included in DAD which is associated with lung fibrosis.
Insights
Acute eosinophilic pneumonia (AEP) shows characteristic histopathology of edema and eosinophil infiltration, distinct from diffuse alveolar damage (DAD). This unique pattern explains AEP's rapid improvement without fibrosis, differentiating it from fibrotic lung diseases.
Area of Science:
- Pulmonary Medicine
- Pathology
- Respiratory Diseases
Background:
- Acute eosinophilic pneumonia (AEP) is a rare condition.
- Previous studies suggest AEP may be a stage of diffuse alveolar damage (DAD) with eosinophilia.
- Other conditions like ARDS, AIP, and IPF share DAD histopathology but have different clinical courses and outcomes.
Purpose of the Study:
- To investigate the histopathology of AEP.
- To determine the presence of DAD phases in AEP cases.
- To differentiate AEP from other DAD-associated lung diseases.
Main Methods:
- Histopathological analysis of 16 AEP cases (2 surgical, 14 transbronchial biopsies).
- Assessment for different phases of diffuse alveolar damage (DAD) via histopathology.
Main Results:
- AEP histopathology shows alveolar edema, eosinophil/lymphocyte infiltration, and interstitial edema.
- Fibrinous exudates were present in alveolar spaces; no hyaline membranes or significant fibrosis observed.
- Findings are consistent with radiological lung edema, explaining rapid clinical improvement.
Conclusions:
- Characteristic AEP histopathology includes edema and eosinophilic infiltration, without fibrosis.
- AEP should be distinguished from diffuse alveolar damage (DAD) due to the absence of fibrosis.
- Histopathological findings support the rapid and complete recovery observed in AEP patients.
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