Base de dados : LILACS
Pesquisa : C16.131.433 [Categoria DeCS]
Referências encontradas : 25 [refinar]
Mostrando: 1 .. 10   no formato [Detalhado]

página 1 de 3 ir para página          

  1 / 25 LILACS  
              next record last record
seleciona
para imprimir
Fotocópia
Texto completo SciELO Costa Rica
Texto completo
Texto completo
Id: biblio-1002563
Autor: Rojas Solano, María Jesús; Badilla García, Jenny.
Título: Hernia diafragmatica en pediatria / Diaphragmatic hernia in pediatrics
Fonte: Med. leg. Costa Rica;36(1):101-109, ene.-mar. 2019.
Idioma: es.
Resumo: Resumen La hernia diafragmática (HD) consiste en un trastorno en el desarrollo del músculo diafragmático, produciéndose el paso de contenido abdominal a la cavidad torácica. Las principales son hernia de Bochdalek, Morgagni y Hiatal.1 Malformación congénita que afecta a 1 de cada 2 200 recién nacidos. Está asociada a elevada morbimortalidad, principalmente por hipoplasia pulmonar e hipertensión.2 La ecografía prenatal determina el diagnóstico, pronóstico y terapia. La cirugía consiste en cerrar el defecto, siendo el objetivo del tratamiento mantener un adecuado intercambio gaseoso, evitar o minimizar la hipoplasia y la hipertensión pulmonar.1 Las hernias diafragmáticas presentes en el momento del nacimiento se diagnostican fácilmente. En contraste, el diagnóstico de las hernias después del periodo neonatal es muy variable, puede conducir a evaluaciones clínicas y radiológicas erróneas.3

Abstract The diaphragmatic hernia is a disorder in the development of the diaphragm, causing the passage of the abdominal contents into the thoracic cavity. The main ones are Bochdalek, Hiatal and Morgagni hernias1. Congenital malformation that affects 1 in 2 200 newborns. It is associated to high morbidity and mortality mainly due to lung hypoplasia and hypertension.2 Prenatal ultrasound determines the diagnosis, prognosis and therapy. The surgical procedure consists ofthe closure of the defect. The goal of the treatment is to maintain adequate gas exchange, to prevent or minimize hypoplasia and pulmonary hypertension.1 Congenital diaphragmatic hernias present at birth are readily recognized. In contrast, the diagnosis of diaphragmatic hernia after the neonatal period varies considerably owing to misleading clinical and radiologic features.3
Descritores: Pediatria
Diafragma
Diagnóstico Clínico
Cavidade Torácica
Hérnias Diafragmáticas Congênitas/diagnóstico por imagem
Hérnia Diafragmática
Limites: Humanos
Tipo de Publ: Revisão
Responsável: CR1.1 - BINASSS - Biblioteca Nacional de Salud y Seguridad Social


  2 / 25 LILACS  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo SciELO Brasil
Texto completo
Id: biblio-973464
Autor: Figueira, Rebeca Lopes; Costa, Karina Miura da; Marsico, Ana Laura; Milani, Thamires Melchiades da Silva; Gonçalves, Walusa Assad; Borges, Marcos de Carvalho; Silva, Orlando Castro e; Sbragia, Lourenço.
Título: Vascular and ventilatory mechanical responses in three different stages of pulmonary development in the rabbit model of congenital diaphragmatic hernia
Fonte: Acta cir. bras;33(10):879-888, Oct. 2018. graf.
Idioma: en.
Resumo: Abstract Purpose: To evaluate the vascular ventilatory response in different stages of lung development and to compare them to the neonates with congenital diaphragmatic hernia (CDH) in a rabbit model. Methods: New Zealand rabbits were divided into 8 groups (n=5): E25, E27, E30, and CDH. All groups were ventilated on a FlexiVent (Scireq, Montreal, QC, Canada), compounding the other 4 groups. The CDH surgery was performed at E25 and the harvest at E30. Dynamic compliance (CRS), dynamic elastance (ERS) and dynamic resistance (RRS) were measured every 4 min/24 min. Median wall thickness (MWT) and airspace were measured. ANOVA Bonferroni tests were used to perform statistical analysis. Significance was considered when p<0.05. Results: CRS was higher in E30 compared to all other groups (p<0.05). CRS and RRS of CDH and E27 were similar and were higher in E25 (p<0.05). MWT was decreased according to the gestational age, was increased in E27V and E30V (p<0.05) and decreased in CDHV (p<0.05), airspace was decreased in E25 and increased in all ventilated groups (p<0.05). Conclusions: The ventilation response of congenital diaphragmatic hernia is like the pseudoglandular stage of the lung development. These findings add information about the physiology of pulmonary ventilation in CDH.
Descritores: Mecânica Respiratória/fisiologia
Hérnias Diafragmáticas Congênitas/fisiopatologia
Pulmão/crescimento & desenvolvimento
-Testes de Função Respiratória
Diafragma/cirurgia
Capacidade Pulmonar Total
Resistência das Vias Respiratórias
Modelos Animais de Doenças
Hérnias Diafragmáticas Congênitas/etiologia
Pulmão/fisiopatologia
Pulmão/irrigação sanguínea
Animais Recém-Nascidos
Limites: Animais
Coelhos
Tipo de Publ: Estudo Comparativo
Responsável: BR1.1 - BIREME


  3 / 25 LILACS  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
Id: biblio-1022807
Autor: Ferrer M, Fernando; Vera, Claudio; Parrao, Guillermo; Coronado, Paula; Urbano, Norma; Vargas, Paula; Theodor, Mónica; Robles, Carolina; Duran, Ruth; Tsunekawa, Harumi; Luco, Matías; Belmar, Cristian; Poblete, José Andrés.
Título: Utilidad de factores pronósticos antenatales en pacientes con hernia diafragmática congénita aislada / Usefulness of antenatal prognostic factors in patients with hernia congenital diaphragmatic isolated
Fonte: ARS med. (Santiago, En línea);43(2):5-11, 2018. Tab, ilus.
Idioma: es.
Resumo: La Hernia Diafragmática Congénita (HDC) corresponde a una malformación del diafragma por la cual los órganos abdominales protruyen hacia la cavidad torácica durante el desarrollo intrauterino. Los recién nacidos afectados presentan grados variables de insuficiencia respiratoria e hipertensión pulmonar, asociándose a una alta morbilidad y mortalidad. Materiales y métodos: Se revisaron los casos de HDC controlados en los períodos pre y post-natal en el Hospital Clínico UC durante el período 2012-2016. Se analizaron los resultados perinatales según distintos factores pronósticos. Resultados: Fueron analizadas 26 embarazadas con diagnóstico de HDC. La sobrevida global fue de un 77% (20/26). La mortalidad global de las pacientes con herniación hepática fue de un 45% (5/11) versus 7% (1/15) en los fetos con hígado no herniado. La mortalidad neonatal fue de un 14% (3/21) en las pacientes con la relación pulmón cabeza (LHR), (observado/ esperado) o/e ≥ a 45% y 60% (3/5) cuando el LHR o/e es < 45%. De las pacientes con LHR o/e ≥ 45%, la necesidad de ECMO fue de un 33% (8/21) mientras que un LHR o/e < 45% fue de un 20% (1/5). Conclusión: La obtención antenatal de un LHR o/e ≥ 45% y ausencia de herniación hepática, son buenos predictores de sobrevida neonatal. La medición de LHR o/e no es capaz de discriminar que pacientes desarrollarán morbilidad respiratoria grave, por lo que debemos buscar nuevos y mejores modelos que permitan seleccionar que pacientes requerirán nacer en un centro con disponibilidad de terapias de soporte vital avanzado como el ECMO neonatal. (AU)

Congenital Diaphragmatic Hernia (CDH) is a malformation of the diaphragm muscle in which the abdominal organs protrude into the thoracic cavity during intrauterine development. Affected newborns have varying degrees of respiratory failure and pulmonary hypertension, associated with high morbidity and mortality. Materials and methods: Controlled HDC cases were reviewed in the pre and post-natal periods at the Clinical Hospital UC during the period 2012-2016. Perinatal results were analyzed according to different prognostic factors. Results: During the 2012-2016 period, 26 pregnant women with a diagnosis of CDH were monitored. The overall mortality of patients with hepatic herniation was 45% (5/11) versus 7% (1/15) in fetuses with a non-herniated liver. Neonatal mortality was 14% (3/21) in patients with o/e (observed/expected) LHR ≥ 45% and 60% (3/5) when the o/e LHR <45%. Of the patients with o/e LHR ≥ 45%, the need for ECMO was 33% (8/21), while a LHR o/e <45% was 20% (1/5). Conclusion: An o/e LHR ≥ 45% and absence of hepatic herniation are good predictors of neonatal survival. The o/e LHR measurement is not capable of identifying which patients will develop severe respiratory morbidity, so we must explore new and better models that allow us to select patients who need to give birth in centers with available advanced life support therapies, such as neonatal ECMO. (AU)
Descritores: Diagnóstico Pré-Natal
Hérnias Diafragmáticas Congênitas
-Oxigenação por Membrana Extracorpórea
Morbidade
Mortalidade
Limites: Humanos
Feminino
Gravidez
Tipo de Publ: Artigo Clássico
Responsável: CL10.1 - Biblioteca Biomédica


  4 / 25 LILACS  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
Id: biblio-838172
Autor: Salas, Gisela; Reusmann, Aixa; Boglione, Mariano; Rubio, Martín; Fumiere, Felicitas; Fariña, Diana.
Título: Hernia diafragmática congénita bilateral de diagnóstico tardío: reporte de un caso / Late diagnosis bilateral congenital diaphragmatic hernia: a case report
Fonte: Arch. argent. pediatr;114(1):e29-e31, feb. 2016. ilus.
Idioma: es.
Resumo: La hernia diafragmática congénita (HDC) es una malformación rara, habitualmente unilateral y más frecuente del lado izquierdo. La HDC bilateral representa el 1% de todas las HDC. La mortalidad es mayor en las HDC derechas y en las bilaterales. Reportamos el caso de un paciente con HDC bilateral, cuya malformación inicialmente se diagnosticó y trató como una HDC derecha. Luego se encontró la presencia de HDC izquierda durante la cirugía de Ladd laparoscópica a los 8 meses de edad.

Congenital diaphragmatic hernia (CDH) is a rare malformation, usually unilateral and left sided. Bilateral CDH (B-CDH) represents 1% of all CDH. Mortality is higher in right side and bilateral defects. We report a case of a patient with Bilateral CDH, initially diagnosed and treated as unilateral right CDH. At 8 months during a laparoscopic Ladd procedure a left side CDH was found.
Descritores: Diagnóstico Tardio
Hérnias Diafragmáticas Congênitas/diagnóstico
Limites: Humanos
Masculino
Recém-Nascido
Tipo de Publ: Relatos de Casos
Responsável: AR94.1 - Centro de Información Pediatrica


  5 / 25 LILACS  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
Id: biblio-1046952
Autor: García González, Juan Ariel; Palermo, Mario S. F.
Título: Hernia diafragmática congénita / Congenital diaphragmatic hernia
Fonte: Prensa méd. argent;104(10):467-477, dic 2018. fig, graf.
Idioma: es.
Resumo: The congenital diaphragmatic hernia (CDH) is a congenital defect of the formation and /or closure of the diaphragm that permits the herniation of abdominal contents into the thorax. It occurs when the diaphragmatic muscle fails to close during the prenatal development, and the contain of the abdomen migrate into the chest through this hole. When the abdominal organs are in the chest, there is limited room for the lungs to grow. This prevents the lungs for developing normally, resulting in pulmonary hypoplasia (or underdeveloped lungs). This can cause reduced blood flow to the lungs and pulmonary hypertension, as well as gastrointestinal reflux, feeding disorders and developmental delays. CDH can occur on the left side, right side or, very rarely, on both sides, and it can be life-threatening. The etiology is usually unknown. The incidence of CDH may be as high as 1 in 2000 to 1 in 5000 newborns alive. The sex relationship male/female is 1:1.8. Because of associated persistent pulmonary hypertension of the newborn and pulmonary hypoplasia, medical therapy in patients with CDH is directed toward optimizing oxygenation while avoiding definitive therapy. No time for repair of CDH is ideal, but it is suggested that the opportunity is 24-48 hours after birth to achieve pulmonary development. The key to survival lies in prompt diagnosis and treatment. Over the past two decades antenatal diagnosis rates have increased the knowledge of the pathophysiology of CDH and has become better understand with advances in clinical care including prenatal surgery, with a reported mortality of almost 35 % in live-born patients and a higher mortality when in utero deaths are conected. All these considerations are described in the article, with special reference to pre and post-natal treatment, complications management, diagnosis and prognosis
Descritores: Cuidado Pós-Natal
Segundo Trimestre da Gravidez
Taxa de Sobrevida
Fetoscopia
Hérnias Diafragmáticas Congênitas/diagnóstico
Hérnias Diafragmáticas Congênitas/embriologia
Hérnias Diafragmáticas Congênitas/fisiopatologia
Limites: Humanos
Feminino
Gravidez
Recém-Nascido
Responsável: AR392.1 - Biblioteca


  6 / 25 LILACS  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
Id: biblio-842913
Autor: Rey, Darío Raúl.
Título: Hernia de Bochdalek / Bochdalek hernia
Fonte: Rev. am. med. respir;15(2):137-138, jun. 2015. ilus.
Idioma: es.
Resumo: Paciente masculino de 80 años, que presenta tos productiva con expectoración MP y fiebre de 6-7 días de evolución. En guardia le practican par radiográfico (Figuras 1 y 2), donde se aprecia opacidad heterogénea en campo inferior derecho, con varias imágenes de tipo cavitario, localizadas en la región posterior. Aorta descendente desenrollada y con extensas calcificaciones. Imagen paratraqueal superior derecha (probable dilatación aneurismática de causa vascular). Es internado con diagnóstico presuntivo de "absceso múltiple en lóbulo inferior derecho". Al examen clínico, llama la atención tanto su buen estado general, como la ausencia de halitosis esperable en esta afección. Al examen clínico, se auscultan roncus en ambas playas pulmonares, con ruidos hidroaéreos asociados en base derecha. Con diagnóstico probable de síndrome canalicular bronquial y hernia de Bochdalek, se practica TC de tórax (Figura 3) que confirma dicha presunción
Descritores: Hérnias Diafragmáticas Congênitas
Hérnia
Responsável: AR423.1 - Biblioteca


  7 / 25 LILACS  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
Id: biblio-1006084
Autor: Cabrera Santos, José; Hidalgo Maldonado, Martha; Beltrán Segovia, Eulalia; Quezada, Cesar.
Título: HERNIA DIAFRAGMÁTICA DE BOCHDALEK EN EL ADULTO: REPORTE DE CASO / Bochdalek diaphragmatic hernia in the adult: case report
Fonte: Rev. Fac. Cienc. Méd. Univ. Cuenca;31(2):76-81, Julio 2013. ilus.
Idioma: es.
Resumo: La hernia de Bochdalek es un defecto congénito de la región posterolateral del diafragma, frecuente en el recién nacido y raro en la edad adulta. En la revisión de la literatura mundial encontramos 130 casos reportados de hernia de Bochdalek en el adulto. El uso de la tomografía computarizada permite el diagnóstico correcto del tipo y localización de la hernia, lo cual facilitará su manejo y elección del tratamiento. La exploración mediante tomografía computarizada multicorte, con posibilidades de realizar reconstrucciones coronales y sagitales, debería ser considerada como método estándar para diagnosticar esta entidad. Para concluir, debemos resaltar que las hernias de Bochdalek en el adulto, asintomáticas, actualmente son descubiertas, en forma incidental, con mayor frecuencia gracias a los avances en las nuevas técnicas de imagen, permitiendo el diagnóstico acertado. Presentamos el caso de una paciente de 33 años, sin sintomatología, que acude al servicio de imagenología del HOSPITAL GENERAL DE III-D.E, con una solicitud médica para trámites personales.

The Bochdalek hernia is a congenital defect localized in the posterior lateral section of the diaphragm, mostly found in newborns but rare in adulthood. In a revision of global literature, we found 130 reported cases of Bochdalek in adulthood. The use of computed tomography lets an accurate diagnosis of the type and the localization of the hernia that will facilitate its management and choice of treatment. Multislice computed tomography screening with the possibility to perform coronal and sagittal reconstructions should be considered as a standard method to diagnose this entity. To conclude, we should highlight that Bochdalek asymptomatic hernias are nowadays accidentally discovered mostly thanks to the technological breakthroughs in imaging, letting us an accurate diagnosis. We present a case study of a 33-year-old patient with no symptomatology who attended the imaging department at the GENERAL HOSPITAL OF III-D.E, with a medical form for personal issues.
Descritores: Diagnóstico por Imagem
Doenças Assintomáticas
Hérnias Diafragmáticas Congênitas
-Tomografia Computadorizada por Raios X
Adulto
Obesidade
Limites: Humanos
Masculino
Adulto
Tipo de Publ: Relatos de Casos
Responsável: EC3.1 - Biblioteca


  8 / 25 LILACS  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
Id: biblio-905199
Autor: Cannizzaro, C M; Gutiérrez, S H; Rubio, C; Nemer, C P; Rodríguez, S P; Fariña, D.
Título: Programa de diagnóstico y tratamiento fetal. Estudio de cohorte sobre su efectividad en la evolución de neonatos con patologías quirúrgicas / Program for prenatal diagnosis and treatment: A cohort study on effectivity on the outcome of newborns with surgical pathologies
Fonte: Med. infant;22(1):26-32, Marzo 2015. tab, ilus.
Idioma: es.
Resumo: Introducción. El diagnóstico prenatal de las malformaciones congénitas (MC) permite optimizar el cuidado perinatal. Al Hospital Garrahan (HG) ingresan recién nacidos (RN) con MC para tratamiento quirúrgico. Desde el año 2008 funciona el programa de diagnostico y tratamiento fetal (PDTF) para optimizar el cuidado prenatal y perinatal de RN con MC. El objetivo del estudio es evaluar el impacto de la derivación prenatal en RN que ingresan a la unidad de cuidados intensivos neonatales (UCIN) del HG por MC seleccionadas. Población y Métodos: estudio observacional analítico y comparativo entre grupos, sobre condición de ingreso y evolución de RN con gastrosquisis (GTQ), mielomeningocele (MMC) y hernia diafragmática (HD) y grado de stress parental, según ingreso a UCIN por derivación prenatal o postnatal. Se realizó análisis bivariado, descriptivo y comparativo de indicadores generales y especiales de cuidado. Resultados: Se incluyeron 164 RN (44 con derivación prenatal a través del PDTF). Este grupo presentó: mejor control del embarazo (93% vs 66%, p: 0.04), menor edad gestacional al diagnóstico (24s vs 33s p=0.0006) y mayor tasa de cesárea electiva (95 vs 47%, p=0.0001). Los RN tuvieron menor necesidad de reanimación e ingresaron más tempranamente a la Unidad (mediana 4hs vs 10hs, p=0,004). Hubo menor stress parental en relación al hijo (17 vs 40%). Los RN con GTQ ingresaron mejor curados y se alimentaron por vía enteral más rápidamente. Conclusión: Los RN con MC derivados prenatalmente a través del PDTF, ingresan precozmente y presentaron mejores estrategias de cuidado que los ingresados por derivación habitual (AU)

Introduction. Prenatal diagnosis of congenital malformations (CM) improve perinatal care. At the Garrahan Hospital (GH) newborns (NB) with CM are admitted for surgical treatment. Since 2008 a program for prenatal diagnosis and treatment (PDT) has been in place to optimize prenatal and perinatal care of NB with CM. The aim of this study was to assess the impact of prenatal referral of NB that are admitted to the GH for selected CM. Population and Methods: An observational, analytical, and between-group comparative study was conducted on the status on admission and outcome in NB with gastroschisis (GS), myelomeningocele (MMC), and diaphragmatic hernia (DH) and degree of parental stress, according to NICU admission after prenatal or postnatal referral. Bivariate, descriptive and comparative analysis of general and specific markers of care was performed. Results: 164 NB were included (44 were prenatally referred through the PDT program). The latter group presented with better pregnancy control (93% vs 66%, p: 0.04), younger gestational age at diagnosis (24w vs 33w p=0.0006), and higher rate of elective cesarean section (95 vs 47%, p=0.0001). This group of NB needed less reanimation and were admitted to the NICU earlier (∑4hs vs 10hs, p=0.004). Parental child-related stress was less (17 vs 40%). NB with GS had a better surgical outcome and were started on enteral feeding earlier. Conclusion: NB with CM that were prenatally referred through the PDT program, were admitted earlier and could be managed with better strategies than those who were conventionally referred (AU)
Descritores: Anormalidades Congênitas/diagnóstico
Anormalidades Congênitas/cirurgia
Gastrosquise/cirurgia
Hérnias Diafragmáticas Congênitas/cirurgia
Meningomielocele/cirurgia
Avaliação de Resultados da Assistência ao Paciente
Diagnóstico Pré-Natal
-Estudos de Coortes
Estudo Comparativo
Estudo Observacional
Assistência Perinatal/tendências
Encaminhamento e Consulta
Limites: Humanos
Recém-Nascido
Responsável: AR305.1 - SID - Servicio de Información y Documentación


  9 / 25 LILACS  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
Id: biblio-876048
Autor: Souza, Hamilton Petry de; Breigeiron, Ricardo; Oliveira, Jéferson Krawcyk de; Tatim, Jerônimo de Ortiz; Costa, Laurence Bedin da.
Título: Hérnia diafragmática congênita simulando tumor de cólon em paciente adulto jovem / Congenital diaphragmatic hernia simulating a colon tumor in young adult patient
Fonte: Rev. AMRIGS;48(4):265-267, out.-dez. 2004. ilus.
Idioma: pt.
Resumo: Os autores apresentam um caso de hérnia diafragmática congênita diagnosticada em paciente adulto jovem durante transoperatório de laparotomia exploradora. Esta, realizada visando a esclarecer quadro clínico sugestivo de obstrução colônica por etiologia neoplásica. É apresentada, ainda, uma revisão sobre o tópico, avaliando-se as semelhanças entre o caso em questão e as informações de literatura (AU)

The authors present a case of congenital diaphragmatic hernia diagnosed in a young adult patient during exploratory laparotomy. Surgery was performed to elucidate clinical findings sugestive of large bowel obstruction due to colonic neoplasia. It Is still presented a review about this subject, evaluating the similarities between the case and the literature informations (AU)
Descritores: Neoplasias do Colo/diagnóstico
Hérnias Diafragmáticas Congênitas/diagnóstico por imagem
-Doenças do Colo/diagnóstico por imagem
Diagnóstico Diferencial
Diafragma/anormalidades
Hérnias Diafragmáticas Congênitas/complicações
Hérnias Diafragmáticas Congênitas/cirurgia
Obstrução Intestinal/etiologia
Limites: Humanos
Feminino
Adulto
Tipo de Publ: Relatos de Casos
Responsável: BR18.1 - Biblioteca FAMED/HCPA


  10 / 25 LILACS  
              first record previous record
seleciona
para imprimir
Fotocópia
Texto completo
Id: biblio-859119
Autor: Loch, Luiz Fernando; Ferrari, Maigrei Dani; Corrêa, Eveline Maciel; Guidolin, Bruno Luiz.
Título: Hérnia diafragmática congênita de apresentação tardia / Late-presenting congenital diaphragmatic hernia
Fonte: Rev. AMRIGS;52(3):212-215, jul.-set. 2008. ilus.
Idioma: pt.
Resumo: Hérnia Diafragmática Congênita (HDC) é um defeito diafragmático em que as vísceras abdominais herniadas para o tórax impedem o desenvolvimento normal dos pulmões. A grande maioria dos pacientes é sintomática nas primeiras 24 horas de vida (90%), devido à grande disfunção respiratória conseqüente. No entanto, esta anomalia pode, mais raramente, passar despercebida até a idade adulta avançada. Dada a raridade da manifestação tardia da HDC, como dificuldade respiratória, este estudo relata o caso de uma criança de 9 meses de idade, com dificuldade respiratória, que após investigação foi diagnosticado HDC (AU)

Congenital Diaphragmatic Hernia (CDH) is a diaphragmatic imperfection where the abdominal viscera protrude to the thorax obstructing the regular development of the lungs. The great majority of affected patients are symptomatic in the first 24 h live (90%) due to the consequent severe respiration dysfunction. Rather rarely, however, this anomaly can pass unnoticed until late adulthood. Given the rarity of late-presenting CDH with respiratory distress, here we report the case of a 9-month-old with respiratory distress who upon investigation was diagnosed as suffering from CDH (AU)
Descritores: Hérnias Diafragmáticas Congênitas/diagnóstico por imagem
Hérnias Diafragmáticas Congênitas/cirurgia
Limites: Humanos
Feminino
Lactente
Tipo de Publ: Relatos de Casos
Responsável: BR18.1 - Biblioteca FAMED/HCPA



página 1 de 3 ir para página          
   


Refinar a pesquisa
  Base de dados : Formulário avançado   

    Pesquisar no campo  
1  
2
3
 
           



Search engine: iAH v2.6 powered by WWWISIS

BIREME/OPAS/OMS - Centro Latino-Americano e do Caribe de Informação em Ciências da Saúde