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    E-ISSN: 2149-4533 ISSN: 1300-865X
    A Rarely Seen Case: Congenital Cystic Adenomatoid Malformation, Type 0
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    Case Report
    VOLUME: 27 ISSUE: 2
    P: 207-211
    August 2022

    A Rarely Seen Case: Congenital Cystic Adenomatoid Malformation, Type 0

    The Bulletin of Legal Medicine 2022;27(2):207-211
    DOI: 10.17986/blm.1565
    Emre Gürbüz 1
    Yusuf Atan 2
    Arzu Akçay 3
    1. Konya Adli Tıp Şube Müdürlüğü, Konya, Türkiye
    2. Bilecik Şeyh Edebali Üniversitesi Tıp Fakültesi, Adli Tıp Anabilim Dalı, Bilecik, Türkiye
    3. Adli Tıp Kurumu Başkanlığı Morg İhtisas Dairesi, Patoloji Uzmanı, İstanbul, Türkiye
    No information available.
    No information available
    Received Date: 18.05.2021
    Accepted Date: 15.09.2021
    Publish Date: 01.08.2022
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    ABSTRACT

    Congenital cystic adenomatoid malformation (CCAM) is a hamartomatous lung anomaly. It constitutes 25% of all congenital lung anomalies and divides 5 subtypes. It is aimed to increase the variety of Type 0 in the literature which is very rare type. A term baby girl at 40th weeks of gestation, from a 19-year-old mother was delivered. The APGAR score of baby was determined 1-1 and baby was intubated. Detection of left sided pneumothorax a chest tube placed. But the baby could not survive after resuscitation period. After the histopathological examination of the lungs it was diagnosed as CCAM Type 0 (bilateral diffuse). By the presented case, this pathology is described with all its detectable aspects, the anomalies that may accompany, how the histopathological samples should be taken. It is intended to be shared with forensic medicine specialists, pathologists and pediatrics specialists.

    Keywords: Congenital cystic adenomatoid malformation, type 0, ventricular septal defect, autopsy, pathology, forensic medicine

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