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Updated: Jun 27, 2025

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Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
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Diffuse Interstitial Lung Disease Revealing Antisynthetase Syndrome
Hanane Benjelloun1, Fatima Ezzahra Haouassia2, Khadija Chaanoune1
1Pulmonology, Ibn Rochd University Hospital, Casablanca, MAR.
Cureus
|May 6, 2024
Summary
Interstitial lung disease (ILD) in connective tissue diseases can reveal Antisynthetase Syndrome (ASS). Early diagnosis and treatment with corticosteroids and cyclophosphamide led to a favorable outcome in a 53-year-old patient.
Area of Science:
- Rheumatology and Pulmonology
- Autoimmune Diseases
- Connective Tissue Diseases
Background:
- Interstitial lung disease (ILD) is a common complication of connective tissue diseases, sometimes being the initial presentation.
- Antisynthetase syndrome (ASS) is a complex autoimmune disorder characterized by specific autoantibodies, notably anti-Jo-1.
- The severity of ILD significantly impacts prognosis and guides treatment strategies in ASS.
Observation:
- A 53-year-old female patient presented with ILD.
- The ILD was the presenting symptom that led to the diagnosis of ASS.
- The patient's condition was monitored during follow-up.
Findings:
- The patient was diagnosed with Antisynthetase Syndrome (ASS) based on the presence of ILD.
- Treatment involved high-dose corticosteroids and cyclophosphamide.
- The patient experienced a favorable clinical evolution following treatment.
Implications:
- This case highlights the importance of recognizing ILD as a potential early sign of ASS.
- Aggressive immunosuppressive therapy, including corticosteroids and cyclophosphamide, can effectively manage ASS-associated ILD.
- Prompt diagnosis and management are crucial for improving patient prognosis in ASS.

