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ctchest radiology clinical diagnosis differential acuteinterstitialpneumonia aip anisocoria causes chronic comparison defects desquamativeinterstitialpneumonia dip disorders druginduced drugrelated findings highattenuation hrct
High Attenuation pattern 1. Chronic eosinophilic pneumonia with peripheral areas of ground glass opacity. 2. Sarcoid end-stage
with peripheral areas ... end-stage with massive fibrosis ... presenting as areas ... #Comparison #Table ... #RadiologyAssistant
The idiopathic interstitial pneumonias (IIPs) comprise a heterogenous group of disorders. They represent fundamental responses of
combinations of fibrosis ... listed in the table ... have specific patterns ... IdiopathicInterstitialPneumonia #ILD ... #Findings #RadiologyAssistant
Anisocoria - Pupillary Defects - Differential Diagnosis Algorithm Physiological - Simple Anisocoria ( <O.5mm) - Anisocoria equal
Differential Diagnosis Algorithm ... Fascicle (Other CN Ill ... Trauma • Tumor (Lung ... , Breast, Thyroid ... #Causes #Ophthalmology
Personality Disorders - Differential Diagnosis Algorithm • Enduring pattern of experience and behaviour that deviates from cultural
Differential Diagnosis Algorithm ... the following areas ... impairment in important areas ... is stable and of ... long duration,
On the left a patient with DIP. The HRCT shows diffuse areas of ground-glass density in the
shows diffuse areas ... and some mosaic pattern ... abnormalities and signs of fibrosis ... DesquamativeInterstitialPneumonia #ILD ... #RadiologyAssistant
On the left a patient who is treated with cytotoxic drugs for a hematologic malignancy. The radiographic
radiographic findings are areas ... patients with a UIP pattern ... or NSIP pattern ... consider drug-related lung ... #RadiologyAssistant
Chronic hypersensitivity pneumonitis (2) The case on the left shows an inspiratory and expiratory scan: the mosaic
with areas of ground-glass ... attenuation and areas ... Signs of fibrosis ... mid and lower lung ... #RadiologyAssistant
Acute interstitial pneumonia (AIP, earlier named Hamman Rich Pneumonitis) is a rare idiopathic lung disease characterized
rare idiopathic lung ... with subsequent fibrosis ... The histologic pattern ... There are areas ... and extensive areas
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