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ctchest radiology clinical diagnosis idiopathic interstitial lymphocyticinterstitialpneumonitis pathophysiology pm pneumonia polymyositis pulmonary signs vasculitis
The idiopathic interstitial pneumonias (IIPs) comprise a heterogenous group of disorders. They represent fundamental responses of
of NSIP, UIP, OP ... and LIP have been ... Interstitial #Pneumonia #IdiopathicInterstitialPneumonia ... #ILD #Findings ... #RadiologyAssistant
The predominant finding is ground glass opacity (GGO). There is very subtle traction bronchiectasis, indicating that the
The predominant finding ... distribution of UIP ... the diagnosis dermatomyositis ... #NonspecificInterstitialPneumonia ... #ILD #RadiologyAssistant
The predominant finding is ground glass opacity (GGO). There is very subtle traction bronchiectasis, indicating that the
The predominant finding ... distribution of UIP ... the diagnosis dermatomyositis ... #NonspecificInterstitialPneumonia ... #ILD #RadiologyAssistant
Dermatomyositis (DM) and Polymyositis (PM): Pathogenesis and clinical findings Elevated Antinuclear Antibodies: Anti-Jo-1, Anti-OJ, Anti-Mi2, Anti-SRP, Anti-EJ,
Dermatomyositis ... (DM) and Polymyositis ... diffuse CD8+ T lymphocytes ... primarily deltoids and hip ... Pathophysiology #Signs #Symptoms
Lymphocytic interstitial pneumonitis or LIP is uncommon, being seen mainly in patients with autoimmune disease, particularly
Lymphocytic interstitial ... pneumonitis or LIP ... syndrome with LIP ... LymphocyticInterstitialPneumonitis #LIP ... #ILD #RadiologyAssistant
In the images on your left you can appreciate again the spectrum of findings seen in
the spectrum of findings ... seen in NSIP. ... cases, excluding UIP ... #NonspecificInterstitialPneumonia ... #ILD #RadiologyAssistant
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