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Updated: Oct 13, 2025

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Atezolizumab-induced scleroderma: a rare complication.
Christon Grant1, Varun Chalasani2, Jeffrey M Uchin3
1Department of Rheumatology, Allegheny Health Network, Pittsburgh, Pennsylvania, USA.
Programmed death-ligand 1 (PD-L1) inhibitor-induced scleroderma is rare. This case report identifies a potential autoantibody association (anti-PM/SCL-75) and suggests early diagnosis aids management.
Area of Science:
- Oncology
- Immunology
- Dermatology
Background:
- Programmed death-ligand 1 (PD-L1) inhibitors are increasingly used for metastatic non-small cell lung cancer.
- Immune-related adverse events (irAEs) are known complications of PD-L1 inhibitors.
- Scleroderma is a rare irAE, with limited published data on its clinical features and management.
Observation:
- A female patient in her 60s developed skin thickening after initiating atezolizumab for non-small cell lung cancer.
- Histological examination confirmed scleroderma.
- The patient tested positive for the anti-PM/SCL-75 antibody.
Findings:
- Discontinuation of atezolizumab and initiation of mycophenolate mofetil led to mild improvement in skin thickening.
- The anti-PM/SCL-75 antibody may be associated with PD-L1 inhibitor-induced scleroderma.
- Early diagnosis of this rare complication is crucial.
Implications:
- This case highlights the importance of recognizing scleroderma as a potential irAE of PD-L1 inhibitors.
- Testing for scleroderma-associated autoantibodies, such as anti-PM/SCL-75, may facilitate earlier diagnosis.
- Prompt identification and management can potentially limit morbidity in patients with this rare condition.
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