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Pulmonary histopathological alterations in patients with acute respiratory failure: an autopsy study
Alexandre de Matos Soeiro1, Edwin Roger Parra, Mauro Canzian
1Faculdade de Medicina da Universidade de São Paulo - FMUSP, University of São Paulo School of Medicine, São Paulo, Brazil.
Objective:
To present the pulmonary histopathological alterations found in the autopsies of patients with acute respiratory failure (ARF) and determine whether underlying diseases and certain associated risk factors increase the incidence of these histopathological patterns.
Methods:
Final autopsy reports were reviewed, and 3030 autopsies of patients > 1 year of age with an underlying disease and associated risk factors were selected. All had developed diffuse infiltrates and died of ARF-related pulmonary alterations.
Results:
The principal pulmonary histopathological alterations resulting in immediate death were diffuse alveolar damage (DAD), pulmonary edema, lymphocytic interstitial pneumonia (LIP) and alveolar hemorrhage. The principal underlying diseases were AIDS, bronchopneumonia, sepsis, liver cirrhosis, pulmonary thromboembolism, acute myocardial infarction (AMI), cerebrovascular accident, tuberculosis, cancer, chronic kidney failure and leukemia. The principal associated risk factors were as follows: age > 50 years; arterial hypertension; congestive heart failure; chronic obstructive pulmonary disease; and diabetes mellitus. These risk factors and AIDS correlated with a high risk of developing LIP; these same risk factors, if concomitant with sepsis or liver cirrhosis, correlated with a risk of developing DAD; thromboembolism and these risk factors correlated with a risk of developing alveolar hemorrhage; these risk factors and AMI correlated with a risk of developing pulmonary edema.
Conclusion:
Pulmonary findings in patients who died of ARF presented four histopathological patterns: DAD, pulmonary edema, LIP and alveolar hemorrhage. Underlying diseases and certain associated risk factors correlated positively with specific histopathological findings on autopsy.
Insights
Pulmonary autopsy findings in patients with acute respiratory failure (ARF) revealed four main histopathological patterns: diffuse alveolar damage (DAD), pulmonary edema, lymphocytic interstitial pneumonia (LIP), and alveolar hemorrhage. Underlying diseases and risk factors influenced these patterns.
Area of Science:
- Pulmonary Pathology
- Critical Care Medicine
- Forensic Pathology
Background:
- Acute respiratory failure (ARF) is a critical condition with significant mortality.
- Understanding the pulmonary histopathological alterations in ARF is crucial for diagnosis and management.
- Autopsy findings provide definitive insights into the terminal pulmonary pathology.
Purpose of the Study:
- To document the spectrum of pulmonary histopathological alterations in patients who died from ARF.
- To investigate the association between underlying diseases, risk factors, and specific histopathological patterns in ARF.
Main Methods:
- Retrospective review of 3030 autopsy reports of patients aged >1 year with ARF.
- Inclusion criteria: underlying disease, associated risk factors, diffuse infiltrates, and ARF-related pulmonary alterations.
- Analysis of histopathological findings and correlation with clinical data.
Main Results:
- The primary histopathological patterns identified were diffuse alveolar damage (DAD), pulmonary edema, lymphocytic interstitial pneumonia (LIP), and alveolar hemorrhage.
- Common underlying diseases included AIDS, sepsis, bronchopneumonia, and cancer.
- Key risk factors were age >50, hypertension, diabetes, and chronic obstructive pulmonary disease (COPD).
- Specific correlations were observed: AIDS with LIP; sepsis/liver cirrhosis with DAD; thromboembolism with alveolar hemorrhage; AMI with pulmonary edema, all in conjunction with risk factors.
Conclusions:
- Four main histopathological patterns (DAD, pulmonary edema, LIP, alveolar hemorrhage) characterize ARF deaths.
- Underlying diseases and specific risk factors are significantly associated with distinct histopathological findings in ARF patients.
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