Congenital cystic adenomatoid malformation presentation of 11 cases and literature review

Jozef Kobos; Damian Młynarski; Bartosz Bogusz; Wojciech Górecki

doi:10.5114/pjp.2020.103716

eISSN: 2084-9869
ISSN: 1233-9687

Polish Journal of Pathology

Current issue Archive Manuscripts accepted About the journal Supplements Editorial board Abstracting and indexing Subscription Contact Instructions for authors Publication charge Ethical standards and procedures

Editorial System

Submit your Manuscript

Editorial Policies

Sarajevo Declaration on Integrity and Visibility of Scholarly Publications

Open access

4/2020
vol. 71

Send email

Copy url:

abstract:

Original paper

Congenital cystic adenomatoid malformation presentation of 11 cases and literature review

Jozef Kobos

¹

,

Damian Młynarski

²

,

Bartosz Bogusz

³

,

Wojciech Górecki

³

Department of Histology and Embryology, Chair of Anatomy and Histology, Medical University of Lodz, Poland
Department of Pathology, University Children’s Hospital of Krakow, Poland
Department of Pediatric Surgery, Jagiellonian University Medical College, University Children’s Hospital of Krakow, Poland

Pol J Pathol 2020; 71 (4): 353-356

DOI: https://doi.org/10.5114/pjp.2020.103716

Online publish date: 2021/02/22

View full text Get citation

PlumX metrics:

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.

keywords:

Congenital cystic adenomatoid malformation presentation of 11 cases and literature review

Jozef Kobos 1 , Damian Młynarski 2 , Bartosz Bogusz 3 , Wojciech Górecki 3

congenital cystic adenomatoid malformation, CCAM, lung lesion, respiratory tract disorder

Jozef Kobos

¹

,

Damian Młynarski

²

,

Bartosz Bogusz

³

,

Wojciech Górecki

³