Pulmonary hypoplasia presenting as persistent tachypnoea in the first few months of life.

Abstract

Over the past two years four infants with persistent tachypnoea have been referred to this hospital. All were subsequently found to have pulmonary hypoplasia. Two (cases 1 and 2) were self referred from the local population. The third had been admitted under the care of a general paediatrician in this hospital (CMMS), and the fourth case was discovered by chance. All the infants had been born in this hospital, for which the delivery rate is about 3500 a year. ### CASE 1 This boy was born by normal delivery at 39 weeks' gestation after an uneventful pregnancy; he weighed 2960 g. He was seen on the postnatal ward at 12 hours of age for grunting and poor feeding. A chest x ray taken at the time was consistent with transient tachypnoea of the newborn. He was discharged at 5 days of age but remained tachypnoeic. At 3 weeks of age he was admitted with fever and coryzal symptoms, pronounced tachypnoea, and poor feeding. Examination was unremarkable apart from a respiratory rate of 70/minute with mild intercostal recession. The coryzal illness resolved but he continued to be tachypnoeic. An electrocardiogram and an echocardiogram did not disclose any abnormalities. He was referred for lung function testing at the age of 4 months because of parental anxiety. His functional residual capacity measured by whole body plethysmography was 16.9 ml/kg indicating pulmonary hypoplasia. In our laboratory the normal mean is 29.8 ml/kg (range 17.6-42 ml/kg). Over the first year his respiratory rate gradually settled to 30-35/minute at rest. A repeat measurement at 12 months of age was 20 ml/kg, showing “catch up” lung growth. ### CASE 2 Born …