Severe liver dysfunction in an infant with cystic fibrosis masquerading as metabolic liver disease.

We present a rare presentation of cystic fibrosis with neonatal cholestasis. Histological features of mucoviscidosis were present in liver involving the biliary tract, intestinal mucosa, pancreas, and lung. Besides, there was a rare association with autosomal dominant type of polycystic renal disease.

Primary Lung Abscess in Early Infancy.

Background: Lung abscess is rare in early infancy. Case characteristics: We report two infants with lung abscess, who presented with short respiratory illness.Intervention: Infants were managed with broad spectrum antibiotics including Clindamycin. Needle aspiration was attempted in one case. Message: High index of suspicion in infants with respiratory distress of prolonged duration can help in reaching the diagnosis.