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BMJ Case Rep ; 20152015 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-26670891

RESUMO

The management of neonatal autosomal recessive polycystic kidney disease (ARPKD) complicated by severe pulmonary insufficiency presents complex clinical challenges. Where massive nephromegaly exists, early bilateral nephrectomy, supportive peritoneal dialysis and early aggressive nutrition can minimise infant mortality. Consensus, however, is lacking on the role and optimal timing of nephrectomy, with decision-making driven by the patient's clinical condition and the expertise of the centre. We report on our experience of an infant with ARPKD requiring neonatal renal replacement therapy and survival at 14 months following early bilateral nephrectomy.


Assuntos
Rim Policístico Autossômico Recessivo/cirurgia , Ecocardiografia , Feminino , Seguimentos , Humanos , Lactente , Masculino , Nefrectomia/métodos , Diálise Peritoneal/métodos , Rim Policístico Autossômico Recessivo/diagnóstico , Gravidez , Resultado do Tratamento
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