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CASE REPORT
Year : 2019  |  Volume : 12  |  Issue : 4  |  Page : 352-355

Spontaneous resolution of a congenital multicystic lung lesion in a newborn


1 Department of Paediatrics, Federal Medical Centre, Birnin Kudu, Nigeria
2 Department of Radiology, Federal Medical Centre, Birnin Kudu, Nigeria
3 Department of Paediatrics, Federal Teaching Hospital, Gombe, Nigeria
4 Department of Paediatrics, Aminu Kano Teaching Hospital, Bayero University Kano, Kano, Nigeria

Correspondence Address:
Halima Umar Ibrahim
Department of Paediatrics, Federal Medical Centre, Birnin Kudu
Nigeria
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/mjdrdypu.mjdrdypu_100_18

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Congenital cystic adenomatous malformation (CCAM) is a rare developmental abnormality of the lung occurring in 1–35,000 live births. In most cases, the outcome of a fetus with CCAM is very good whereas in some cases, it can be life-threatening. It is usually discovered in neonates because of respiratory distress. Spontaneous resolution of CCAM has been reported as rare. We report a case of spontaneous resolution of CCAM in a 21-day-old-female baby with respiratory distress and chest X-ray suggestive of multicystic lesion of the left lung.


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