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Estudio y manejo de la malformación congénita de la vía aérea pulmonar presentación de una serie de cincos casos y revisión de la literatura
| Content Provider | Semantic Scholar |
|---|---|
| Author | Nimer, Lubna Nasr El Aboultaif, Liliana Aboultaif Jáuregui, Yoleida Colmenares, Tamara Godoy, Yamil Conti, Tomasina Álvarez, Juan Manuel Martínez Sierra, Luis |
| Copyright Year | 2013 |
| Abstract | La malformacion congenita de la via aerea pulmonar es una displasia pulmonar focal caracterizada por presentar tejido pulmonar multiquistico y estructuras bronquiales. Esta patologia es diagnosticada predominantemente durante el periodo neonatal y en raras ocasiones durante la infancia. En este trabajo se presentan cinco casos de malformacion congenita de la via aerea pulmonar, con reportes tomograficos de multiples imagenes quisticas de tamanos y diametros diferentes. Tras la realizacion de lobectomia y estudio anatomopatologico tres de los casos se clasificaron como tipo 1 y dos como tipo 2 segun la Armed Forces Institute of Pathology. Debido a la infrecuencia de esta patologia, a la escasa literatura nacional y a la particular presentacion en edad escolar, en este trabajo se describen 5 casos con el fin de contribuir con el estudio, diagnostico y manejo de pacientes con esta patologia. Study and management of congenital pulmonary airwa malformation presenting of a series of five cases and review of the literature Abstract Congenital pulmonary airway malformation is a focal pulmonary dysplasia characterized by multicystic and bronchial structures in alveoli lung tissue. This condition is diagnosed predominantly in neonatal period and on rare occasions during childhood. In this paper we present five cases of congenital pulmonary airway malformation, in all cases the CT scan showed different sizes and diameters multiple cystic images. After lobectomy and athological analysis three cases were classified as type 1 and two as type 2, according to Armed Forces Institute of Pathology. Because the infrequency of this disease, lack of local literature and schoolchildren presentation, we describe in this paper five cases in order to contribute to the study, diagnosis and management of patients with this condition. |
| Starting Page | 16 |
| Ending Page | 22 |
| Page Count | 7 |
| File Format | PDF HTM / HTML |
| Volume Number | 2 |
| Alternate Webpage(s) | http://erevistas.saber.ula.ve/index.php/biomedicina/article/download/4283/4066 |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |