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Updated: Feb 25, 2026

Oropharyngeal Administration of Bleomycin in the Murine Model of Pulmonary Fibrosis
Published on: May 9, 2025
PULMONARY LESIONS ASSOCIATED WITH BLEOMYCIN THERAPY IN MALIGNANCIES
J R Bhardwaj1, K Kartik2, S Sambandam3
1Professor & Head, Pune-411 040.
Bleomycin treatment for malignancy can cause severe lung damage, including interstitial pneumonitis and fibrosis. Autopsy studies reveal these pulmonary lesions often affect the lower lobes and mimic metastatic nodules.
Area of Science:
- Pulmonary Pathology
- Oncology
- Toxicology
Background:
- Bleomycin is a chemotherapy agent used to treat various cancers.
- Drug-induced lung injury is a significant concern in cancer patients undergoing treatment.
- Understanding the specific pulmonary manifestations of bleomycin is crucial for patient management.
Purpose of the Study:
- To investigate the autopsy findings of pulmonary lesions in patients treated with bleomycin.
- To characterize the histological changes and distribution of these lesions.
- To correlate clinical symptoms with pathological findings.
Main Methods:
- Autopsy examination of seven patients with malignancy treated with bleomycin.
- Histopathological analysis of lung tissue.
- Correlation of findings with clinical data, including respiratory distress.
Main Results:
- Pulmonary lesions were observed in all studied patients, with a predilection for lower lobes and subpleural areas.
- All cases showed diffuse alveolar damage progressing to interstitial pneumonitis.
- Histological changes included proteinaceous exudate, interstitial fibrosis, and epithelial dysplasia resembling metastatic nodules.
Conclusions:
- Bleomycin treatment is associated with significant pulmonary toxicity.
- The observed lung lesions can present with respiratory distress and mimic metastatic disease.
- These findings highlight the importance of monitoring pulmonary function in patients receiving bleomycin.
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05:45A Refined Aerosol-Based Intratracheal Bleomycin Delivery Method for Reproducible and Minimally Invasive Mouse Models of Pulmonary Fibrosis
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