Co-Existence of Congenital Cystic Adenomatoid Malformation and Pulmonary Sequestration in a Newborn with Spontaneous Pneumothorax: A Case Report and Review of the Literature

Congenital bronchopulmonary malformations are uncommon anomalies of infants and children presenting as congenital lobar emphysema, bronchogenic cyst, congenital cystic adenomatoid malformation (CCAM), or pulmonary sequestration (PS). CCAM is the second most common congenital lung malformation in new...

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Bibliographic Details
Published in:Haseki tıp bülteni 2019-06, Vol.57 (2), p.211-214
Main Authors: Cebeci, Burcu, Erener Ercan, Tuğba, Babayiğit, Arslan, Ağırgöl, Esra, Büyükkale, Gökhan, Çetinkaya, Merih
Format: Article
Language:English
Subjects:
Babies
Case reports
Congenital cystic adenomatoid malformation
Congenital diseases
Coronary vessels
Cysts
hybrid congenital lung malformation
Lung diseases
newborn
Patients
Pediatrics
Pneumonia
pulmonary sequestration
Sağlık Hizmetleri
Surgeons
Tıp
Ultrasonic imaging
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Summary:Congenital bronchopulmonary malformations are uncommon anomalies of infants and children presenting as congenital lobar emphysema, bronchogenic cyst, congenital cystic adenomatoid malformation (CCAM), or pulmonary sequestration (PS). CCAM is the second most common congenital lung malformation in newborns. There are five types of CCAM based on the embryologic and the histologic features. PS is defined as a mass of tissue developing in the lung but having no respiratory function. PS is classified into two types: extralobar and intralobar. Co-existence.of CCAM and PS is a rare occurrence. Hybrid lesions, especially type 2 CCAM and PS combination may have a more severe clinical progress. Herein, we report a male infant with type 2 CCAM in combination with PS who died despite both medical and surgical treatment.
ISSN:1302-0072
2147-2688
DOI:10.4274/haseki.galenos.2018.4225