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dc.contributor.authorGarzi, Alfredo
dc.contributor.authorFerrentino, Umberto
dc.contributor.authorArdimento, Gaetano
dc.contributor.authorBrongo, Sergio
dc.contributor.authorRubino, Maria Serena
dc.contributor.authorCalabrò, Eleonora
dc.contributor.authorClemente, Ennio
dc.contributor.authorDi Crescenzo, Rosa Maria
dc.date.accessioned2020-06-30T12:34:50Z
dc.date.available2020-06-30T12:34:50Z
dc.date.issued2019
dc.identifier.citationGarzi A, Ferrentino U, Ardimento G, Brongo S, Rubino MS, Calabrò E, Clemente E, Di Crescenzo RM. Congenital cystic adenomatoid malformation of the lung tipe II: three cases report. Translational Medicine @ UniSa 2019, 20(2): 4-8.it_IT
dc.identifier.issn2239-9747it_IT
dc.identifier.urihttp://www.translationalmedicine.unisa.it/indexit_IT
dc.identifier.urihttp://elea.unisa.it:8080/xmlui/handle/10556/4604
dc.identifier.urihttp://dx.doi.org/10.14273/unisa-2796
dc.description.abstractCongenital cystic adenomatoid malformation (CCAM) is a rare congenital lung lesion. It may appear since birth (30-35%) with difficulty breathing or may have a late onset (60- 65%) with recurring pulmonary infections or growth failure; in a small percentage of cases, the lesion can be completely asymptomatic. Fetal or post-natal surgery can be used as surgical treatment of these lesions. Postnatal surgery consists of a lobectomy, bilobectomy or pneumonectomy, based on the size of the lesion. The best age to undergo this surgery is around 2 years, but only if the injury is stable and the child has no complications. The study describes three cases of CCAM, observed at the Pediatric Surgery Section of the University of Siena. We analyzed those 3 cases whose approach was defined by the onset of symptoms, age and clinical condition of patients. In the first case the surgery was performed a few hours after birth due to the worsening of the clinical conditions; in the other two cases it was delayed because the patients were asymptomatic. The purpose of this study is to review the management of patients with CCAM in relation to clinical onset and the type of injury.it_IT
dc.format.extentP. 4-8it_IT
dc.language.isoenit_IT
dc.sourceUniSa. Sistema Bibliotecario di Ateneoit_IT
dc.subjectCongenital cystic adenomatoid malformation (CCAM)it_IT
dc.subjectCongenital pulmonary airway malformation (CPAM)it_IT
dc.subjectBronchopulmonary sequestrationit_IT
dc.subjectCongenital bronchopulmonary malformationit_IT
dc.subjectSparing surgeryit_IT
dc.titleCongenital cystic adenomatoid malformation of the lung tipe II: three cases reportit_IT
dc.typeArticleit_IT
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