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pubmed-article:11956788rdf:typepubmed:Citationlld:pubmed
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pubmed-article:11956788pubmed:dateCreated2002-4-16lld:pubmed
pubmed-article:11956788pubmed:abstractTextWe report the rare case of an 11-year-old boy who presented with intractable hypoxaemia and a pulmonary mass. Investigations revealed this to be a pulmonary arteriovenous malformation. It was entirely confined to the right middle lobe and was successfully treated via a right middle lobectomy. The relevant literature with respect to both diagnosis and treatment is reviewed.lld:pubmed
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pubmed-article:11956788pubmed:authorpubmed-author:CurrieBBlld:pubmed
pubmed-article:11956788pubmed:authorpubmed-author:TongA KAKlld:pubmed
pubmed-article:11956788pubmed:authorpubmed-author:La HeiE RERlld:pubmed
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pubmed-article:11956788pubmed:volume18lld:pubmed
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pubmed-article:11956788pubmed:pagination168-70lld:pubmed
pubmed-article:11956788pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:11956788pubmed:year2002lld:pubmed
pubmed-article:11956788pubmed:articleTitleCongenital pulmonary arteriovenous malformations.lld:pubmed
pubmed-article:11956788pubmed:affiliationDepartment of Surgery, Sydney Children's Hospital, Randwick, NSW, Australia.lld:pubmed
pubmed-article:11956788pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11956788pubmed:publicationTypeCase Reportslld:pubmed