Neonatal pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasia.

نویسندگان

  • S Koppen
  • C R W Korver
  • M Dalinghaus
  • C J J Westermann
چکیده

A 3 week old infant presented with persistent hypoxaemia and was diagnosed with pulmonary arteriovenous malformations. Her family history was positive for hereditary haemorrhagic telangiectasia. She was treated successfully with coil embolotherapy at the age of 4 months. Transcatheter embolisation may be considered the primary treatment for pulmonary arteriovenous malformations in infancy.

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عنوان ژورنال:
  • Archives of disease in childhood. Fetal and neonatal edition

دوره 87 3  شماره 

صفحات  -

تاریخ انتشار 2002