Congenital Cystic Adenomatoid Malformation (CCAM) Type II: A Rare Case of Sudden Infant Death
Congenital cystic adenomatoid malformation (CCAM) is a developmental lesion of the lungs and terminal respiratory structures, which is characterized by pseudocysts, lesions, and cystically dilated airways. CCAM is also known as congenital pulmonary airway malformation (CPAM). Various classification...
Main Authors: | Monica Salerno, Francesco Sessa, Giuseppe Cocimano, Salvatore Roccuzzo, Massimiliano Esposito, Cristoforo Pomara |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-11-01
|
Series: | Children |
Subjects: | |
Online Access: | https://www.mdpi.com/2227-9067/9/12/1830 |
Similar Items
-
Congenital cystic adenomatoid malformation of lung in adults: 2 rare cases report and review of the literature
by: Feng Anning, et al.
Published: (2012-04-01) -
Cystic adenomatoid malformation of the lung: A diagnostic dilemma
by: Mohta Anup, et al.
Published: (2009-01-01) -
A complete spectrum of congenital cystic adenomatoid malformation of the lung deceptive clinical presentations and histological surprises; a single institutional study from a tertiary care hospital in North India
by: Nazia Manzoor Walvir, et al.
Published: (2023-01-01) -
Tension pneumothorax in a toddler with congenital cystic adenomatoid malformation
by: Jayalaxmi Shripati Aihole
Published: (2021-06-01) -
Congenital cystic adenomatoid malformation of lung: A case report
by: Asish Banerjee, et al.
Published: (2015-06-01)