Congenital cystic adenomatoid malformation presentation of 11 cases and literature review

Autor:	Bartosz Bogusz, Wojciech Górecki, Damian Młynarski, Józef Kobos
Rok vydání:	2020
Předmět:	medicine.medical_specialty business.industry General Medicine Pathology and Forensic Medicine Lung lesion ccam medicine Congenital Cystic Adenomatoid Malformation lung lesion Medicine Radiology congenital cystic adenomatoid malformation Presentation (obstetrics) business respiratory tract disorder
Zdroj:	Polish Journal of Pathology, Vol 71, Iss 4, Pp 353-356 (2021)
ISSN:	1233-9687 2015-2019
DOI:	10.5114/pjp.2020.103716
Popis:	The aim of the study was to present cases of congenital cystic adenomatoid malformation (CCAM) in terms of pathological features, gender and site distribution as well as to compare the results with Stocker’s classification. A retrospective review was performed on eleven cases of CCAM obtained in 4-years period (2015-2019) in University Children’s Hospital in Krakow, in Poland. The cases for this study were 7 boys and 4 girls (64% vs. 36%). Patients age at surgery ranged from 4 days to 10 months. 6 cases involved the left lung (55%) whereas the right lung was involved in 5 cases (45%). Histopathological examination showed congenital cystic adenomatoid malformation type I in 7 cases (64%), type II in 3 cases (27%) and type III in 1 case (9%). No congenital cystic adenomatoid malformation type 0 nor IV was diagnosed. Data obtained from this study correspond to Stocker’s classification, showing that the most common CCAM types are those associated with good prognosis. Histopathological features should always confirm the nature of the lesion, that is initially suspected in the imaging examination.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77296aa8996ebe91c3594c1e71f8eeef https://doi.org/10.5114/pjp.2020.103716 Zobrazit plný text záznamu