Özet:

Congenital cystic adenomatoid malformation (KKAM) is a hamartomatic lung anomaly that accounts for 1/4 of all parental lungs anomalies. Five subtypes are separated. It is intended to increase the variety of facts in the literature of the very rare type 0 with the present fact. In the 40th week of pregnancy, a female baby was given birth. The postpartum APGAR score was identified as 1-1 and was treated for non-spontaneous breathing and taken for newborn intensive care. On the left, pnömotoraks was detected because of the breast tube was resuscitated but exitus was accepted when no response was received. In the histopathological examination of the samples taken from the lungs in the autopsy, the diagnosis of cystic adenomatoid malformation Type 0 (bilateral diffuse) was found. The presented phenomenon and all aspects of this pathology can be identified, the anomalies that can be accompanied, how histopatological samples should be taken and the newborn deaths in the ethology that may have a similar history-medical resume, with the aim of emphasizing the memory of the anomalies of KKAM, all of these aspects are shared with the specialists of judicial medicine, pathology and pediatrics.

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