Anti-PL-7 Antisynthetase Syndrome
Imaging findings
An older woman presents with fairly symmetric lower lung zone opacity on radiograph with possible small effusions, and CT shows dilated airways with traction bronchiectasis and a lower lobe-predominant consolidation pattern similar to the preceding anti-Jo-1 case.
Key takeaways
Antisynthetase antibody testing was positive for anti-PL-7 rather than anti-Jo-1, the most common antisynthetase antibody, and these antibodies tend to be mutually exclusive so typically only one is positive; the patient later developed a rash and myositis. Even after treatment and partial improvement of the consolidation, the basal-predominant traction bronchiectasis persisted, illustrating that fibrotic change from antisynthetase-syndrome ILD can be only partially reversible.
AI-assisted summary — may contain errors. Verify against the source video. Learn more
More from this webinar
- Bronchopulmonary Sequestration with Bronchial AtresiaCongenital
- Intra-arterial Pulmonary Metastases from ChondrosarcomaNeoplastic
- Paget-Schroetter Syndrome (Effort Thrombosis of the Subclavian Vein)Vascular
- Loeys-Dietz SyndromeCongenital
- Cervical Aortic Arch with Aberrant Subclavian Artery in DiGeorge SyndromeCongenital
- Anti-Jo-1 Antisynthetase SyndromeILD
- Solitary Pulmonary AmyloidomaMetabolic
- Brown Tumors from Renal Osteodystrophy (Secondary Hyperparathyroidism)Metabolic
See all cases from April 14, 2018 →
Related ILD cases
- Fibrotic Hypersensitivity Pneumonitis (Indeterminate for UIP Pattern)
- Acute Hypersensitivity Pneumonitis from Vaping Marijuana
- Radiation-Induced Migratory Organizing Pneumonia After Breast Cancer Treatment
- Hypersensitivity Pneumonitis Misdiagnosed as Sarcoidosis
- Combined Smoking-Related Lung Disease with Overlapping LCH and RB-ILD/DIP Features
- Severe Smoking-Related Lung Disease Improving After Smoking Cessation