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Four months later, the patient developed diffuse interstitial pulmonary infiltrates with mediastinallymphadenopathy.
2
From our experience, marked enhancement on CT and no signal intensity on MRI in PALBV could differentiate this anomaly from mediastinallymphadenopathy.
3
Computed tomography (CT) scan of the chest revealed lung infiltrates with air bronchogram of the right middle lobe and mediastinallymphadenopathy.