A Rarely Seen Case: Congenital Cystic Adenomatoid Malformation, Type 0
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 40<sup>th</sup> week...
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Adli Tıp Uzmanları Derneği
2022-08-01
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| Series: | Adli Tıp Bülteni |
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http://adlitipbulteni.com/archives/archive-detail/article-preview/a-rarely-seen-case-congenital-cystic-adenomatoid-m/52519
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| _version_ | 1797915433246916608 |
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| author | Emre Gürbüz Yusuf Atan Arzu Akçay |
| author_facet | Emre Gürbüz Yusuf Atan Arzu Akçay |
| author_sort | Emre Gürbüz |
| collection | DOAJ |
| description | 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 40<sup>th</sup> 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. |
| first_indexed | 2024-04-10T12:42:58Z |
| format | Article |
| id | doaj.art-60216f35208545a69cd1cb80787bba01 |
| institution | Directory Open Access Journal |
| issn | 1300-865X 2149-4533 |
| language | English |
| last_indexed | 2024-04-10T12:42:58Z |
| publishDate | 2022-08-01 |
| publisher | Adli Tıp Uzmanları Derneği |
| record_format | Article |
| series | Adli Tıp Bülteni |
| spelling | doaj.art-60216f35208545a69cd1cb80787bba012023-02-15T16:14:14ZengAdli Tıp Uzmanları DerneğiAdli Tıp Bülteni1300-865X2149-45332022-08-0127220721110.17986/blm.156513049054A Rarely Seen Case: Congenital Cystic Adenomatoid Malformation, Type 0Emre Gürbüz0Yusuf Atan1Arzu Akçay2 Konya Adli Tıp Şube Müdürlüğü, Konya, Türkiye Bilecik Şeyh Edebali Üniversitesi Tıp Fakültesi, Adli Tıp Anabilim Dalı, Bilecik, Türkiye Adli Tıp Kurumu Başkanlığı Morg İhtisas Dairesi, Patoloji Uzmanı, İstanbul, Türkiye 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 40<sup>th</sup> 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. http://adlitipbulteni.com/archives/archive-detail/article-preview/a-rarely-seen-case-congenital-cystic-adenomatoid-m/52519 congenital cystic adenomatoid malformationtype 0ventricular septal defectautopsypathologyforensic medicine |
| spellingShingle | Emre Gürbüz Yusuf Atan Arzu Akçay A Rarely Seen Case: Congenital Cystic Adenomatoid Malformation, Type 0 Adli Tıp Bülteni congenital cystic adenomatoid malformation type 0 ventricular septal defect autopsy pathology forensic medicine |
| title | A Rarely Seen Case: Congenital Cystic Adenomatoid Malformation, Type 0 |
| title_full | A Rarely Seen Case: Congenital Cystic Adenomatoid Malformation, Type 0 |
| title_fullStr | A Rarely Seen Case: Congenital Cystic Adenomatoid Malformation, Type 0 |
| title_full_unstemmed | A Rarely Seen Case: Congenital Cystic Adenomatoid Malformation, Type 0 |
| title_short | A Rarely Seen Case: Congenital Cystic Adenomatoid Malformation, Type 0 |
| title_sort | rarely seen case congenital cystic adenomatoid malformation type 0 |
| topic | congenital cystic adenomatoid malformation type 0 ventricular septal defect autopsy pathology forensic medicine |
| url |
http://adlitipbulteni.com/archives/archive-detail/article-preview/a-rarely-seen-case-congenital-cystic-adenomatoid-m/52519
|
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