Successful Management of Rapidly Progressive Interstitial Pneumonia With Autoimmune Features in an Elderly Patient: A Case Report
Yudai Tanaka, Ryuichi Ohta, Chiaki Sano

TL;DR
An elderly man with rapidly progressive interstitial pneumonia and autoimmune features was successfully treated with aggressive immunosuppressive therapy and tailored care.
Contribution
This case report demonstrates the effectiveness of early diagnosis and intensive treatment in managing severe autoimmune-related interstitial pneumonia in elderly patients.
Findings
Cyclophosphamide pulse therapy significantly improved the patient's condition within days.
Multidisciplinary care and tailored treatment led to functional recovery and discharge.
Early immunological evaluation and aggressive therapy are crucial for managing this condition in elderly patients.
Abstract
An 82-year-old man presented with acute respiratory distress, a one-week history of dry cough, and worsening dyspnea. Chest computed tomography revealed bilateral diffuse ground-glass opacities, raising suspicion of rapidly progressive interstitial pneumonia. Rapid autoantibody testing confirmed interstitial pneumonia with autoimmune features (IPAF), likely triggered by an upper respiratory infection. Initial treatment with high-dose steroid pulse therapy was insufficient to stabilize the patient’s respiratory status. Cyclophosphamide pulse therapy was initiated on day 4, resulting in significant improvement by day 7. The patient’s oxygen requirements steadily decreased, and follow-up imaging showed near-complete resolution of lung abnormalities. Intensive immunosuppressive therapy, infection control measures, and tailored supportive care enabled functional recovery and discharge to a…
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Taxonomy
TopicsInterstitial Lung Diseases and Idiopathic Pulmonary Fibrosis · Antifungal resistance and susceptibility · Respiratory and Cough-Related Research
