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1.
Arch Pediatr ; 18(3): 331-7, 2011 Mar.
Artigo em Francês | MEDLINE | ID: mdl-21292458

RESUMO

Pulmonary atresia and critical pulmonary stenosis with intact ventricular septum includes a wide spectrum of cardiopathies with great morphological heterogeneity. The pulmonary valve may be completely atretic or may contain a puncture hole if stenosis is present. The obstruction may be membranous and/or muscular. All components of the right ventricle can be affected, even the coronary circulation with ventriculocoronary connections and stenosis or atresia of the pulmonary arteries. Prenatal diagnosis is made when the right ventricle is hypoplastic and hypertrophic. The pulmonary valve is thickened and the pulmonary artery is perfused retrogradely through the ductus arteriosus. Right ventriculocoronary connections may sometimes be seen with fetal echocardiography. Postnatal survival depends on the patency of the ductus arteriosus, requiring prostaglandin E1 infusion. When hypoplastic right ventricle and/or ventricle-dependent coronary circulation exists, biventricular circulation is not possible. In these cases, surgical treatment is palliative. In cases with well-developed right ventricle, transcatheter therapy is usually provided with perforation and balloon dilation of the pulmonary valve. In cases of muscular obstruction of the right ventricle outflow tract, surgery may be considered as first-line therapy. In case of prenatal diagnosis, the medical termination of pregnancy is possible when severe right ventricular hypoplasia exists, precluding biventricular circulation. Postnatally, the prognosis of the patients is highly variable, mainly related to the size of the right cavities and the presence of coronary anomalies.


Assuntos
Atresia Pulmonar/diagnóstico , Atresia Pulmonar/terapia , Estenose da Valva Pulmonar/diagnóstico , Estenose da Valva Pulmonar/terapia , Aborto Induzido , Cateterismo , Diagnóstico Diferencial , Feminino , Cardiopatias Congênitas/diagnóstico , Humanos , Recém-Nascido , Gravidez , Diagnóstico Pré-Natal
2.
Unfallchirurgie ; 10(4): 182-91, 1984 Aug.
Artigo em Alemão | MEDLINE | ID: mdl-6485135

RESUMO

Within a period of twelve years, the authors have treated twelve patients with metacarpophalangeal joint luxations of thumb and long fingers which could not be reposed by conservative treatment. The case reports are presented in order to describe the problems posed by this relatively rare injury, the reasons hindering a reposition, and the treatment methods. This study is intended to underline the importance of early diagnosis and immediate surgical treatment in order to maintain the function of the joint.


Assuntos
Traumatismos dos Dedos , Luxações Articulares/cirurgia , Articulação Metacarpofalângica/lesões , Adolescente , Adulto , Criança , Pré-Escolar , Feminino , Humanos , Luxações Articulares/diagnóstico por imagem , Ligamentos Articulares/lesões , Masculino , Articulação Metacarpofalângica/diagnóstico por imagem , Pessoa de Meia-Idade , Músculos/lesões , Complicações Pós-Operatórias/diagnóstico por imagem , Radiografia , Traumatismos dos Tendões , Polegar/lesões , Cicatrização
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