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Large congenital cystic asdenomatous malformation of the lung in a newborn
Author(s) -
İlyas Yolbaş,
Selvi Kelekçi,
Yusuf Kenan Haspolat,
Ali Güneş,
Velat Şen
Publication year - 2013
Publication title -
dicle tıp dergisi
Language(s) - English
Resource type - Journals
eISSN - 1308-9889
pISSN - 1300-2945
DOI - 10.5798/diclemedj.0921.2013.04.0354
Subject(s) - medicine , lung
Congenital cystic adenomatous malformation (CCAM) oflung is a rare form of congenital hamartomatous lesionsof the lung consisting of cysts filled with air. The generalclinic presentation of CCAM is dyspnea in newborns.CCAM may mimic congenital pneumonia or respiratorydistress syndrome. After the delivery, the newborn malewho had low Apgar score and severe respiratory distresswas intubated and admitted to neonatal intensive careunit. Patient was ventilated for 50 days and weaned fromthe mechanical ventilator at 50th day. Type II CCAM of thelung was diagnosed according to the chest radiographsand computed tomography scan signs. Although the surgeonssuggested lobectomy considering the patient’s notcompletely asymptomatic, family did not accept this operationdue to the risk of death. The patient was dischargedfrom the hospital until the next control.Key word: Congenital cystic adenomatous malformation of lunch, newborn, conservative treatmen

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